FDA News Releases

• Date Index

• Chapel Hill Creamery Recalls Cheese Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Gel Spice, Inc. Issues Alert on Elevated Lead Levels in One Lot of Fresh Finds Ground Turmeric Powder, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: CareFusion Recalls AVEA Ventilator Due to an Electrical Issue Which May Cause an Unexpected Shutdown, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Compliance Date Extension for Certain Vending Machine Calorie Disclosures, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - AVEA Ventilator by CareFusion: Class I Recall - Electrical Issue May Cause Unexpected Shutdown, FDA MedWatch
• CFSAN Constituent Update - CFSAN Address Change, U.S. Food & Drug Administration (FDA)
• FDA approves Adlyxin to treat type 2 diabetes, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Good Dog, Bad Food: Foods for People That Are Bad for Your Dog, U.S. Food & Drug Administration (FDA)
• General Mills Expands Retail Flour Recall, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Announces FY 2017 Animal Drug User Fee Rates for ADUFA and AGDUFA, U.S. Food & Drug Administration (FDA)
• Let's Do Lunch, Inc., dba Integrated Food Service, Expands Voluntary Recall, U.S. Food & Drug Administration (FDA)
• Meijer Recalls Fresh Salad Products Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA updates warnings for fluoroquinolone antibiotics, U.S. Food & Drug Administration (FDA)
• Opportunity to Comment: Blood Donor Deferral Policy for Reducing the Risk of Human Immunodeficiency Virus Transmission by Blood and Blood Products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fluoroquinolone Antibacterial Drugs for Systemic Use: Drug Safety Communication - Warnings Updated Due to Disabling Side Effects, FDA MedWatch
• FDA Hepatitis Update - Approval of VIEKIRA XR extended release fixed dose combination tablets, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Electronic System for Milk Products Export Lists, U.S. Food & Drug Administration (FDA)
• Voluntary Recall for 30 Bakery Products, U.S. Food & Drug Administration (FDA)
• Allergen Alert: Kitchen Cravings Strawberry and Mixed Berry Parfaits with trace peanuts, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Stryker Sustainability Solutions Recalls Flush Angiographic Catheter Due to Tip Separation, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HCG and Sermorelin by Talon Compounding Pharmacy: Recall - Lack of Sterility Assurance, FDA MedWatch
• Talon Compounding Pharmacy Issues Voluntary Nationwide Recall of HCG and Sermorelin Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
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  • Talon Compounding Pharmacy Issues Voluntary Nationwide Recall of HCG and Sermorelin Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Starway Inc. Issues Allergy Alert on Undeclared Milk and Unallowed Color Ponceau 4R (E124) in Peony Mark Brand Biscuits, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Angiodynamics Soft Vu Omni Flush Angiographic Catheter by Stryker Sustainability Solutions (formerly Ascent Healthcare Solutions): Class I Recall - Tip Separation, FDA MedWatch
• Hy-Vee Voluntarily Recalls a Limited Quantity of Its No-Salt-Added Black Beans Due to Potential Presence of Foreign Material, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Survey and Data from Ongoing Sampling Program, U.S. Food & Drug Administration (FDA)
• Krispak, Inc. Issues Allergy Alert on Undeclared Treenuts - Pecans In GFS Honey Roasted Peanuts Received From Supplier Trophy Nut Co., U.S. Food & Drug Administration (FDA)
• Agave Dream Recalls Cappuccino Ice Cream Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medwatch Safety Alert: WEN by Chaz Dean Cleansing Conditioners: FDA Statement - Investigation of Adverse Event Reports, FDA Office of Women's Health
• ConAgra Foods Expands Recall of P.F. Chang’s Home Menu Brand Meals Available in Grocery Retailers Due to Potential Presence of Foreign Material ConAgra Foods Does Not Make Meals for P.F. Chang’s Restaurants, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Draft Revised Guidance for Industry Available, U.S. Food & Drug Administration (FDA)
• Faribault Foods, Inc. Announces Voluntary Recall of a Limited Quantity of No-Salt-Added Black Beans (Frijoles Negros Bajo En Sodio, Frijoles Negros, Frijol Negro Sin Sal) Due to the Potential Presence of Foreign Material, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - WEN by Chaz Dean Cleansing Conditioners: FDA Statement - Investigation of Adverse Event Reports, FDA MedWatch
• Theo Chocolate Issues Allergy Alert on Undeclared Milk in Salted Almond 70% Dark Chocolate, U.S. Food & Drug Administration (FDA)
• Update: Tippin’s Gourmet Pies, LLC Announces the Recall of Tippin’s Key Lime Pie for the Presence of Undeclared Peanut Residue Due to Supplier Recall, U.S. Food & Drug Administration (FDA)
• PharmaTech LLC Issues Voluntary Nationwide Recall of Diocto Liquid Distributed by Rugby Laboratories Due to Product Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Oral Liquid Docusate Sodium by PharmaTech : Recall - Contaminated with B. cepacia, FDA MedWatch
• FDA approves first intraocular lens with extended range of vision for cataract patients, U.S. Food & Drug Administration (FDA)
• Monogram Appetizers Issues Allergy Alert On Undeclared (Egg) In Poppers Brand Mozzarella Cheese Sticks, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Releases Foods and Veterinary Medicine Strategic Plan, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FVM Strategic Plan, U.S. Food & Drug Administration (FDA)
• International Commissary Corporation Issues Voluntary Recall of Marie Callender's Cheese Biscuit Mix Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Issues Final Rule under FSMA to Update Food Facility Registration, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Issues Final Rule under FSMA to Update Food Facility Registration, U.S. Food & Drug Administration (FDA)
• Kerry Inc. Recalls Golden Dipt Jalapeno Breaders Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products, U.S. Food & Drug Administration (FDA)
• Baptista's Bakery Issues Allergy Alert on Undeclared Milk in Snack Factory Original Pretzel Crisps, U.S. Food & Drug Administration (FDA)
• Two Flavors of Betty Crocker Cake Mix Recalled, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - INRatio and INRatio2 PT/INR Monitor System by Alere: Recall - Potentially Inaccurate INR Results, FDA MedWatch
• The July 2016 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Alere to Initiate Voluntary Withdrawal of the Alere INRatio and INRatio2 PT/INR Monitor System, U.S. Food & Drug Administration (FDA)
• Read about Summer Safety, Osteoporosis and more, FDA Office of Women's Health
• FDA approves new medication for dry eye disease, U.S. Food & Drug Administration (FDA)
• General Mills Voluntarily Recalls a Limited Quantity of Frozen Beyond Meat Vegetarian Indian Curry with Beyond Chicken, U.S. Food & Drug Administration (FDA)
• FDA approves first MRI-guided focused ultrasound device to treat essential tremor, U.S. Food & Drug Administration (FDA)
• Who You Gonna Call?..., FoodSafety.gov
• Kroger Recalls Deluxe S'mores Ice Cream Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Continental Mills Recalls Blueberry Pancake Mix Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Hearn Kirkwood Recalls "Evie's Cheddar Potato Salad" Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Differin Gel 0.1% for over-the-counter use to treat acne, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Vending Machine Calorie Disclosures Compliance Date, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listing of Veterinary Master Files, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - June 2016 Safety Labeling Changes includes 42 products with revisions to Prescribing Information, FDA MedWatch
• FDA advances Precision Medicine Initiative by issuing draft guidances on next generation sequencing-based tests, U.S. Food & Drug Administration (FDA)
• Federal court orders Alabama seafood company to cease production due to food safety violations, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals July 2016 Update, U.S. Food & Drug Administration (FDA)
• Mister Cookie Face LLC, a Subsidiary of Fieldbrook Foods Corporation, Announces a Voluntary Recall of Sundae Shoppe Ice Cream Dipped Variety Cones for the Possible Presence of Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• FDA approves first absorbable stent for coronary artery disease, U.S. Food & Drug Administration (FDA)
• Cumberland Farms Announces Voluntary Recall of Sea Salt Caramel Delights Flavor of Cumberland Farms Premium Chocolate Treats Due to Possible Presance of Peanuts, U.S. Food & Drug Administration (FDA)
• Dream Body Weight Loss Issues Voluntary Nationwide Recall of Dream Body 450mg, Dream Body Extreme Gold 800mg, Dream Body Advanced 400mg Due to Undeclared Sibutramine, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listings of Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
• General Mills Expands Flour Recall to Include Additional Dates from Last Fall, U.S. Food & Drug Administration (FDA)
• Eastland Food Corp. Issues Allergy Alert on Undeclared Milk in Euro Custard Cakes, U.S. Food & Drug Administration (FDA)
• Order a FREE Summer Safety Kit today!, FDA Office of Women's Health
• CVM Updates - FDA Fifth Biannual Progress Report on Judicious Use of Antimicrobials in Food-producing Animals, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: HeartWare Inc. Extends Recall to Include Batteries Used in the Ventricular Assist Device Due to Premature Power Depletion, U.S. Food & Drug Administration (FDA)
• FDA clears first test to detect specific genetic markers for certain antibiotic-resistant bacteria directly from clinical specimens, U.S. Food & Drug Administration (FDA)
• FDA Basics Webinar- June 30, 2016: Vaccines for Use in Pregnancy to Protect Young Infants from Disease, U.S. Food & Drug Administration (FDA)
• FDA approves implantable device that changes the shape of the cornea to correct near vision, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HeartWare Ventricular Assist Device (HVAD) Batteries by HeartWare Inc.: Class I Recall - Premature Power Depletion, FDA MedWatch
• CFSAN Constituent Update - FDA to Extend Comment Period on Draft Guidance for Industry: Action Level for Inorganic Arsenic in Rice Cereals for Infants, U.S. Food & Drug Administration (FDA)
• FDA requests additional information to address data gaps for consumer hand sanitizers, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Comment Period on Raw Manure as Fertilizer Extended, U.S. Food & Drug Administration (FDA)
• Statement from FDA Commissioner Robert Califf, M.D. announcing the acting director of the FDA Oncology Center of Excellence, U.S. Food & Drug Administration (FDA)
• FDA approves Epclusa for treatment of chronic Hepatitis C virus infection, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Purina Animal Nutrition Initiates Recall of Purina Medicated Sheep Feed due to Elevated Copper Level, U.S. Food & Drug Administration (FDA)
• IKEA N.A. Services, LLC Issues Allergy Alert on Undeclared Milk, Almond, Hazelnut in the CHOKLAD MORK and CHOKLAD MORK 70% Dark Chocolate Bars, Net Wt. 3.5 oz., U.S. Food & Drug Administration (FDA)
• Purina Animal Nutrition Initiates Recall of Purina Medicated Sheep Feed due to Elevated Copper Level, U.S. Food & Drug Administration (FDA)
• What You Need to Know About Home Canning, FoodSafety.gov
• Sunflower kernel recall impacts Nature Valley Protein Chewy Bars & Nature Valley Simple Nut Bars, U.S. Food & Drug Administration (FDA)
• Recall For Undeclared Allergen Taken as Part of FDA's Safety Advisory Regarding Grain Craft Flour Recall, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - GenomeTrakr Transforming Food Safety, U.S. Food & Drug Administration (FDA)
• Figi's Issues Recall Alert Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Creative Snacks Co. Issues Allergy Alert on Undeclared Peanuts and Soy in Select The Fresh Market Smoked TFM Supreme Nut Mix Bags, U.S. Food & Drug Administration (FDA)
• Learn the Facts About Opioids, FDA Office of Women's Health
• Michael’s® Naturopathic Programs Issues Allergy Alert on Undeclared Milk and Soy in The Dietary Supplement Cholesterol Metabolism Factors™, U.S. Food & Drug Administration (FDA)
• Mondelēz Global LLC Conducts Nationwide Voluntary Recall of Limited Quantity of Honey Maid Teddy Grahams Cinnamon Cubs Product Sold in Foodservice Channels in the U.S., U.S. Food & Drug Administration (FDA)
• Atlantic Spice Recalls Sunflower Seeds Roasted Salted, Tropical Mix and Cranberry Health Mix Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Radagast Pet Food, Inc. Is Voluntarily Recalling Four Lots Of Frozen Rad Cat Raw Diet Due To Possibly Salmonella And Listeria Monocytogenes Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Radagast Pet Food, Inc. Is Voluntarily Recalling Four Lots Of Frozen Rad Cat Raw Diet, U.S. Food & Drug Administration (FDA)
• Bolthouse Farms Voluntarily Recalls Protein Beverages Due to Possible Spoilage, U.S. Food & Drug Administration (FDA)
• Snyder’s-Lance Is Issuing an Allergy Alert for Lance Oyster Crackers, U.S. Food & Drug Administration (FDA)
• Kellogg Company Voluntarily Recalls Certain Graham Products, U.S. Food & Drug Administration (FDA)
• Update: Tippin's Gourmet Pies, LLC Announces the Recall of Tippin's Key Lime Pie for the Presence of Undeclared Peanut Residue Due to Supplier Recall, U.S. Food & Drug Administration (FDA)
• Updated: National Frozen Foods Corporation Recalls Frozen Green Peas and Frozen Mixed Vegetables Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Marin Foods Specialties, Inc. Recalls Raw Macadamia Nuts Sold at Whole Foods Market® Stores in CA, NV, OR, and WA Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Pinnacle Foods Inc. Voluntarily Recalls Limited Quantity of C&W Early Harvest Petite Peas and C&W Petite Peas Due to Possible Listeria Contamination, U.S. Food & Drug Administration (FDA)
• Greenland Trading Corporation Recalls Al Rasheed Sardine Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Continuing Medical Education Video about the Nutrition Facts Label Now Available, U.S. Food & Drug Administration (FDA)
• Dutch Treat Foods Recalls Sweet Pea Pasta Salad Because of Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Molly & Drew Voluntarily Recalls Three Lots of American Original Beer Bread Mix Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Let's Do Lunch, Inc., dba Integrated Food Service, Voluntarily Recalls Certain Ready-To-Eat Sandwiches Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Fresh Express Issues Precautionary Recall of a Small Quantity of Caesar Salad Kits Due to an Undeclared Walnut Allergen, U.S. Food & Drug Administration (FDA)
• Eillien's Candies Inc. Voluntarily Recalls Various Sizes and Brands of Snack Products Containing Roasted-Salted Sunflower Kernels and Roasted-Unsalted Sunflower Kernels Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Minor Use/Minor Species (MUMS) Grant Application Open Period Due August 12, 2016, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Reminds Retail Establishments of Upcoming Changes to the Use of Antibiotics in Food Animals, U.S. Food & Drug Administration (FDA)
• National Frozen Foods Corporation Recalls Frozen Green Peas and Frozen Mixed Vegetables Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Green Cuisine Recalls Pesto Pasta Salad with Arugula Sold in Select Whole Foods Market Stores Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Updates for Prezista (darunavir) for use in pregnant women, U.S. Food & Drug Administration (FDA)
• GMJ Natural Products, Inc. Issues Allergy Alert on Undeclared Whey Protein in "Jugo Moringa Plus Antioxidant 32 Fl Oz Jug", U.S. Food & Drug Administration (FDA)
• Earnest Eats Recalls Earnest Eats Dark Chocolate Almond Chewy Granola Bars Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HP Hood LLC Voluntarily Recalls Protein Drinks From Its Sacramento Facility Due To Premature Spoilage, U.S. Food & Drug Administration (FDA)
• Gardner Pie Company Issues Allergy Alert on Cheesecakes and Key Lime Pies Sold Between 4/11/16 and 6/14/16 Due to Potential Undeclared Peanut Residue, U.S. Food & Drug Administration (FDA)
• Tippin's Gourmet Pies, LLC Announces the Recall of Tippin's Key Lime Pie for the Presence of Undeclared Peanut Residue Due to Supplier Recall, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA to Hold Webinar on New Nutrition Facts Label, U.S. Food & Drug Administration (FDA)
• Zupan's Markets Initiates Voluntary Recall of Macaroni Salad With Cheddar Cheese Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kashi Company Expands Date Codes of Two Products Related to Previously Announced Recall of Snack Bars and Bear Naked Granola, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces 2016 Stakeholder Meetings on Reauthorization of Two Animal Drug User Fee Programs, U.S. Food & Drug Administration (FDA)
• Crescent Specialty Foods Inc. Recalls Raw Pistachios Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HelloFresh Recalls Frozen Peas Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Essential Foods Recalls Four Flavors of Globespun Gourmet Wraps Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kroger Supplier Expands Sunflower Products Recall, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update: Sweet Productions, Inc., U.S. Food & Drug Administration (FDA)
• Armour-Eckrich Meats Recalls Armour Snackmakers Keebler Animal Crackers Due to the Presence of Undeclared Peanut Residue, U.S. Food & Drug Administration (FDA)
• Frito-Lay Issues Allergy Alert on Undeclared Milk In Select Spicy Sweet Chili Doritos Tortilla Chips, U.S. Food & Drug Administration (FDA)
• Sinosharp Issues Allergy Alert on Undeclared Milk Allergens in "Chocolate Flavored Cookies", U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: IFSAC Analysis Improves Understanding of Foodborne Illness Attribution, U.S. Food & Drug Administration (FDA)
• Read about clinical trials, HIV and more, FDA Office of Women's Health
• Mars Chocolate North America Issues Allergy Alert for Select Varieties of Combos For Potential Undeclared Peanut Residue, U.S. Food & Drug Administration (FDA)
• Simple Health LLC Announces The Recall of Tosi Cappuccino Crunch SuperBites For Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Canagliflozin (Invokana, Invokamet) and Dapagliflozin (Farxiga, Xigduo XR): Drug Safety Communication - Strengthened Kidney Warnings, FDA MedWatch
• CFSAN Constituent Update - Public Workshops on Menu Labeling, U.S. Food & Drug Administration (FDA)
• Honey Bunchie, LLC Recalls a Limited Number of Gourmet Honey Bars That Contain SunOpta Sunflower Kernels due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kellogg Company Voluntarily Recalls Certain Snacks for Potential Undeclared Peanut Residue Due to Flour Supplier Recall, U.S. Food & Drug Administration (FDA)
• Creative Snacks Co. Issues Further Expanded Recall on Sunflower Seeds and Trail Mixes Including Sunflower Seeds Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update to Frito-Lay Recall of Select Rold Gold Tiny Twists, Rold Gold Thins, Rold Gold Sticks and Rold Gold Honey Wheat Braided, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Zecuity (sumatriptan) Migraine Patch: UPDATED Drug Safety Communication - FDA Evaluating Risk of Burns and Scars, FDA MedWatch
• NoGii Voluntarily Recalls Nuts About Berries Paleo Bars Because of Possible Health Risk Related to Sunflower Seeds, U.S. Food & Drug Administration (FDA)
• FDA approves vaccine to prevent cholera for travelers, U.S. Food & Drug Administration (FDA)
• Bounce USA Recalls Apple Cinnamon Protein Punch Energy Balls Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Post Consumer Brands Voluntarily Recalls Limited Quantity of Great Grains Protein Blend – Honey, Oats & Seeds Cereal Due to Possible Listeria Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - May 2016 Safety Labeling Changes posting includes 86 products with changes to Prescribing Information, FDA MedWatch
• How to Travel Safely with Dietary Restrictions, FoodSafety.gov
• Giant Eagle Expands Recall of Sunflower Seeds Sold At Select Giant Eagle and Market District Stores in Pittsburgh, U.S. Food & Drug Administration (FDA)
• Giant Eagle Expands Recall of Sunflower Seeds Sold At The Carmel Market District, U.S. Food & Drug Administration (FDA)
• Giant Eagle Expands Recall of Sunflower Seeds Sold At Market District Stores, U.S. Food & Drug Administration (FDA)
• Giant Eagle Expands Recall of Sunflower Seeds Sold At Select Giant Eagle and Market District Stores in Cleveland, U.S. Food & Drug Administration (FDA)
• Fal Foods USA Inc. Issues Allergy Alert on Undeclared Milk in DF Mavens Chocolate Almond Fudge Frozen Bars, U.S. Food & Drug Administration (FDA)
• Hershey Issues Voluntary Recall of SoFit Products Due to Expanded Supplier Recall of Sunflower Seeds, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Webinar on Guidance for Voluntarily Reducing Sodium, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Draft Guidance for Sponsors of Certain Oncology Drugs for Companion Animals, U.S. Food & Drug Administration (FDA)
• FDA targets unlawful internet sales of illegal prescription medicines during International Operation Pangea IX, U.S. Food & Drug Administration (FDA)
• Rucker's Wholesale and Service Co. Recalls Sunflower Kernel, Sweet & Salty Mix, Cajun Hot Mix Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Taylors Candy Inc. Recalls "Stuckey’s Sunflower Kernels" Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nature Made (Various Products) by Pharmavite LLC: Recall - Possible Health Risk, FDA MedWatch
• SunOpta Announces Second Expansion of Voluntarily Recall on Market District Pre-Packaged Bulk Sunflower Seeds Sold at Select Giant Eagle and Market District Stores, U.S. Food & Drug Administration (FDA)
• SunOpta Announces Second Expansion of Voluntarily Recall on Market District Pre-Packaged and Bulk Sunflower Seeds Sold at Market District Stores, U.S. Food & Drug Administration (FDA)
• SunOpta Announces Second Expansion of Voluntarily Recall on Market District Pre-Packaged and Bulk Sunflower Seeds Sold at Select Giant Eagle and Market District Stores, U.S. Food & Drug Administration (FDA)
• Rucker's Makin' Batch Candies Issues Food Recall of Cajun Mix - Because of Possible Health Risk, due to Potential Presence of Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• SunOpta Announces Second Expansion of Voluntarily Recall on Market District Pre-Packaged and Bulk Sunflower Seeds Sold at the Carmel Market District, U.S. Food & Drug Administration (FDA)
• Nature Made® Recalls Various Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Herr Foods Inc. Announces Voluntary Recall of Waffle Works Brand of 4 oz. Double Chocolate Waffle Sandwiches due to Undeclared Milk: Allergy Concern for Those With Milk Allergy, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Loperamide (Imodium): Drug Safety Communication - Serious Heart Problems With High Doses From Abuse and Misuse, FDA MedWatch
• The Body Shot Bar Issues Voluntary Nationwide Recall of Step 2 Due to Undeclared Sibutramine, U.S. Food & Drug Administration (FDA)
• Frito-Lay Issues Voluntary Recall of Select Rold Gold Tiny Twists, Rold Gold Thins, Rold Gold Sticks and Rold Gold Honey Wheat Braided Due to Potential Undeclared Peanut Allergen, U.S. Food & Drug Administration (FDA)
• Atkins Nutritionals, Inc. Issues Voluntary Recall of Certain Products After Sunflower Seed Supplier Expands Recall Due to Listeria Concerns, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Over-the-Counter Antacid Products Containing Aspirin: FDA Drug Safety Communication - Serious Bleeding Risk, FDA MedWatch
• The June 2016 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Nature's One Voluntarily Recalls 'PediaSmart Dairy Vanilla' Because of Possible Under-Delivery of Nutrition Using Included Scoop, U.S. Food & Drug Administration (FDA)
• First Source Expanded Recall Of "Various Products Containing Sunflower Kernels Received From Our Supplier Sunopta" Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Brown & Haley Expands Voluntary Recall of Mountain Thins Trail Mix Flavor Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Hy-Vee Voluntarily Recalls One Salad Topping and Additional Trail Mix Products Due to Expanded Sunflower Seed Recall in the U.S., U.S. Food & Drug Administration (FDA)
• Publix Recalls Nut, Seed and Raisin Mix Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Maranatha Brand Voluntarily Recalls Certain Lots of Sunflower Seed Butter Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kashi Company Voluntarily Recalls Two Varieties of Snack Bars and Two Varieties of Bear Naked® Granola Due to Potential Health Risk After Sunflower Seed Supplier Increases Scope of Impacted Products, U.S. Food & Drug Administration (FDA)
• Hostess Brands, LLC Issues Recall On Possible Undeclared Peanut Residue In Certain Snack Cake And Donut Products, U.S. Food & Drug Administration (FDA)
• Chelsea Food Services Issues Allergy Alert On Undeclared Egg In Product, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Investigates Low Levels of Peanut Residue Found in Limited Flour and Flour Products, U.S. Food & Drug Administration (FDA)
• Updated: Hickory Harvest Expands Recall of Certain Sunflower Kernel Products Because of Possible Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• ACH Food Companies, Inc. Issues Voluntary Recall of Salad Toppings Due to Possible Health Risk Related to Sunflower Seeds, U.S. Food & Drug Administration (FDA)
• Nu Life Market Voluntarily Recalls Sun Life Sunflower Spread Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Approves Entyce, a New Animal Drug for Appetite Stimulation in Dogs, U.S. Food & Drug Administration (FDA)
• Bayou Brothers Issues an Allergy Alert for an Undeclared Fish Allergen in Bayou Brothers Creole Sauce With a "Best By" Date of "23MAR17" Through "18MAY18", U.S. Food & Drug Administration (FDA)
• CVM Updates - An Interview with FDA’s New Deputy Commissioner for Foods and Veterinary Medicine, U.S. Food & Drug Administration (FDA)
• Clif Bar & Company Issues Voluntary Recall of Three Flavors: CLIF BAR Nuts & Seeds Energy Bars, CLIF BAR Sierra Trail Mix Energy Bars, and CLIF Mojo Mountain Mix Trail Mix Bars Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FURTHER EXPANDED Recall Period of Certain Sunflower Kernel Products Due to Possible Contamination by Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Urgent Food Recall of Jungle Jim's Roast No Salt Sunflower Seeds, Windy Acres Fruity Trail Mix & Windy Acres No Salt Sunflower Seeds Due to Potential Presence of Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Additional Quaker Quinoa Granola Bars Recalled as a Result of Expanded Sunflower Kernel Contamination by SunOpta, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Zecuity (sumatriptan) Migraine Patch: Drug Safety Communication - FDA Evaluating Risk of Burns and Scars, FDA MedWatch
• Meadow Gold Dairy in Boise Conducts Voluntary Recall of Whipping Cream and Half and Half Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• June 2016 EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Update of CVM's What's New - Animal Drug Approvals June 2016 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Kashi Company Voluntarily Recalls One Variety of Kashi® Granola Bars and One Variety of Bear Naked® Granola Due to Potential Health Risk Related to Sunflower Seeds, U.S. Food & Drug Administration (FDA)
• Statement from FDA Commissioner Robert Califf, M.D. on the release of the final individual patient expanded access form, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - An Interview with FDA’s New Deputy Commissioner for Foods and Veterinary Medicine, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Stӧckert 3T Heater-Cooler System by Sorin Group Deustchland GmbH: Safety Communication - Reports of Mycobacterium Chimaera Infections, FDA MedWatch
• Medical Device Safety and Recalls: Mycobacterium chimaera Infections Associated with Sorin Group Deustchland GmbH Stӧckert 3T Heater-Cooler System, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Voluntarily Reducing Sodium, U.S. Food & Drug Administration (FDA)
• Gold Medal, Gold Medal Wondra, and Signature Kitchens Flour Recalled Due to Possible E. coli O121 Contamination, U.S. Food & Drug Administration (FDA)
• Expanded Voluntary Recall on Certain Backroad Country Brand Sunflower Kernel Products, U.S. Food & Drug Administration (FDA)
• Sid Wainer and Son Recalls Domaine de Provence La Cucina Tart Shells and Domaine de Provence Neutral 3" Cone Tart Shells Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Whole Foods Market store in California issues consumer advisory on kimchi products due to undeclared food allergens, U.S. Food & Drug Administration (FDA)
• Sweet Earth Natural Foods Issues Voluntary Recall of Mispackaged Big Sur Burritos That Contain the Santa Cruz Burrito: Potential Allergy Concern for Those with Milk Allergy, U.S. Food & Drug Administration (FDA)
• FDA approves new diagnostic imaging agent to detect recurrent prostate cancer, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Medtronic Respiratory and Monitoring Solutions Recalls Battery Pack Used on Patient Monitors Due to Potential Fire Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Hummingbird Med Devices Inc. Recalls Hummi Micro-Draw Blood Transfer Device Due to Potential for Parts to Disconnect, U.S. Food & Drug Administration (FDA)
• How to Have a Food Safe Memorial Day Weekend, FoodSafety.gov
• FDA approves first buprenorphine implant for treatment of opioid dependence, U.S. Food & Drug Administration (FDA)
• Voluntary Recall On Certain Backroad Country Brand Sunflower Kernel Products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hummi Micro-Draw Blood Transfer Device by Hummingbird Med Devices: Class I Recall - Potential for Parts to Disconnect, FDA MedWatch
• CFSAN Constituent Update - Final Food Defense Regulation, U.S. Food & Drug Administration (FDA)
• FDA issues final food defense regulation, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Guidance Regarding the Food Labeling Term “Evaporated Cane Juice”, U.S. Food & Drug Administration (FDA)
• C. J. Dannemiller Co. Annouces Recall of "Sunflower Kernels, Roasted and Salted" and "Sunflower Kernels, Roasted No Salt" Because of Possible Listeria monocytogenes, U.S. Food & Drug Administration (FDA)
• E S Foods Recalls Meal Breaks Containing Sunflower Seeds Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Hickory Harvest Expands Recall of Certain Sunflower Kernel Products Because of Possible Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - RFR Annual Report, U.S. Food & Drug Administration (FDA)
• First Source Recalls "Various Products Containing Sunflower Kernels Received From Our Supplier Sunopta" Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Food Gusto, Inc. Issues Allergy Alert on Undeclared Milk in Birdy 3 in 1 Coffee Mix (Robusta), U.S. Food & Drug Administration (FDA)
• Ultimate Nutrition Issues Allergy Alert on Possible Undeclared Milk Allergen in Amino Gold Products, U.S. Food & Drug Administration (FDA)
• Updated: The Pictsweet Company Notifies Consumers That Select Kroger Brand Frozen Vegetables Shipped into the Western US are Included in Previously Announced Recall, U.S. Food & Drug Administration (FDA)
• Hy-Vee Voluntarily Recalls Six Trail Mix Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Dakota Style Foods, Inc. Recalls Product Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Dakota Style Foods, Inc. Recalls Product Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Papa John's Salad and Produce Recalls Oriental Salad with Sesame Ginger Dressing Due to Possible Listeria monocytogenes Contamination, U.S. Food & Drug Administration (FDA)
• TreeHouse Foods Expands Voluntary Product Recall Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Announces New Nutrition Facts Label, U.S. Food & Drug Administration (FDA)
• The Caramel Factory, LLC Issues An Allergy Alert, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Comment Period extended to July 25, 2016 --FDA seeks public comment on Proposed Rule; Proposal To Ban Electrical Stimulation Devices (ESDs) Used To Treat Self-Injurious or Aggressive Behavior, U.S. Food & Drug Administration (FDA)
• FDA modernizes Nutrition Facts label for packaged foods, U.S. Food & Drug Administration (FDA)
• Expanded Recall Period of Certain Sunflower Kernel Products Due to Possible Contamination By Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update: Warning Letters Highlight Differences Between Cosmetics and Medical Devices, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nizoral (ketoconazole) Oral Tablets: Drug Safety Communication - Prescribing for Unapproved Uses including Skin and Nail Infections Continues; Linked to Patient Death, FDA MedWatch
• FDA MedWatch - Well Care Compounding Pharmacy Sterile Compounded Products: Recall - Lack Of Sterility Assurance, FDA MedWatch
• FDA MedWatch (corrected link) - Canagliflozin (Invokana, Invokamet): Drug Safety Communication - Clinical Trial Results Find Increased Risk of Leg and Foot Amputations, FDA MedWatch
• FDA MedWatch - Canagliflozin (Invokana, Invokamet): Drug Safety Communication - Clinical Trial Results Find Increased Risk of Leg and Foot Amputations, FDA MedWatch
• Well Care Compounding Pharmacy Issues Voluntary Statewide Recall of All Sterile Compounded Products Due to Lack Of Assurance if Sterility Concerns, U.S. Food & Drug Administration (FDA)
• Dr. Praeger's Sensible Foods, Inc. Announces Voluntary Recall of Various Dr. Praeger's and Ungar's Products Related to CRF Frozen Vegetable Recall for Possible Health Risk, U.S. Food & Drug Administration (FDA)
• The Quaker Oats Company Issues Voluntary Recall of Quaker Quinoa Granola Bars Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Webinar: May 17, 2016: Practice the Art of Sun Protection, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Provides Update on Jerky Pet Treat Investigation, U.S. Food & Drug Administration (FDA)
• A Precautionary Recall of Three Cases of The Farmers Market Chopped Asian Salad Kit is Announced Due to Possible Exposure to Allergens, U.S. Food & Drug Administration (FDA)
• Montero Farms Recalls Orange Habanero Peppers Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HMSHost Recalls Multiple Brands of Cape Cod Cranberry Trail Mix Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Hy-Vee Voluntarily Recalls Frozen Hy-Vee Vegetable Fried Rice and Frozen Hy-Vee Chicken Fried Rice Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - CALL FOR ABSTRACTS: 2017 National Food Safety Education Conference, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - April 2016 Drug Safety Labeling Changes includes 29 products with revisions to Prescribing Information, FDA MedWatch
• FDA MedWatch - BiCNU (carmustine for injection): FDA Alert - Counterfeit Product Discovered in Some Foreign Countries, FDA MedWatch
• Voluntary Recall on Piggly Wiggly Brand Yellow Cut Corn, U.S. Food & Drug Administration (FDA)
• SOS Telecom, Inc. Recalls New Unapproved Drugs Marked as Dietary Supplements, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: Draft Guidance for Qualified Facilities under the FSMA Preventive Controls Rules, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CFSAN Constituent Update: Draft Guidance for Qualified Facilities under the FSMA Preventive Controls Rules, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fluoroquinolone Antibacterial Drugs: Drug Safety Communication - FDA Advises Restricting Use for Certain Uncomplicated Infections, FDA MedWatch
• Update of CVM's What's New - Xylitol and Your Dog: Danger, Paws Off, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Issues Final Guidance on Frequently Asked Questions About Medical Foods, U.S. Food & Drug Administration (FDA)
• Publix Recalls Cranberry Nut And Seed Mix Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Issues Allergy Alert on Undeclared Peanut and Coconut in Korean BBQ Sauce, U.S. Food & Drug Administration (FDA)
• Vending Nut Co. recalls Sunflower Kernel Products Because Of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• Read about National Women's Health Week and more, FDA Office of Women's Health
  • <Possible follow-ups>
  • Read about National Women's Health Week and more, FDA Office of Women's Health
• Frontier Co-op Initiates Voluntary Recall of Organic Hojicha Tea Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• United Natural Trading LLC Announces Voluntary Recall of Walnuts, U.S. Food & Drug Administration (FDA)
• World Class Distribution Issues Voluntary Recall on Kale & Edamame Salad Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kroger Recalls Simple Truth Organic Frozen Mix Vegetables after Supplier Listeria Concern, U.S. Food & Drug Administration (FDA)
• Food Recall of Sweet & Salty Trail Mix - Because of Possible Health Risk, Due to Potential Presence of Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Manna Pro Products Issues Limited Voluntary Recall of Chick Starter Medicated Distributed in California, Nevada, Oregon, and Hawaii, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Manna Pro Products Issues Limited Voluntary Recall of Chick Starter Medicated Distributed in California, Nevada, Oregon, and Hawaii, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Olanzapine: Drug Safety Communication - FDA Warns About Rare But Serious Skin Reactions, FDA MedWatch
• CFSAN Constituent Update - Statement on FDA’s Actions on Labeling of KIND Products, U.S. Food & Drug Administration (FDA)
• FDA issues rule for data collection of antimicrobial sales and distribution by animal species, U.S. Food & Drug Administration (FDA)
• NORPAC Foods, Inc. Recalls Natural Directions Organic Mixed Vegetables, And Natural Directions Organic Green Peas, Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Food Recall Of Sweet And Salty Trail Mix –Because Of Possible Health Risk, Due To Potential Presence Of Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• The Pictsweet Company Announces Voluntary Recall of Select Frozen Vegetable Items due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Releases Final Rule Related to the Reporting of Antimicrobial Sales and Distribution Information, U.S. Food & Drug Administration (FDA)
• Kroger Recalls Broccoli Raisin Salad After Supplier Listeria Concern, U.S. Food & Drug Administration (FDA)
• Let's Talk Health, Inc. Issues Alert on Undeclared Milk and Soy in Energizer Drink Mix, U.S. Food & Drug Administration (FDA)
• The Pictsweet Company Notifies Consumers that Select Kroger Brand Frozen Vegetables Shipped into the Western US are Included in Previously Announced Recall, U.S. Food & Drug Administration (FDA)
• Bickel’s Snack Foods Recalls Golden Gourmet Veggie Chips Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Ajinomoto Windsor Recall of Products Related to CRF Frozen Vegetable Recall, U.S. Food & Drug Administration (FDA)
• CVM Updates - Virtual attendance Available for the ADUFA/AGDUFA Public Meetings, U.S. Food & Drug Administration (FDA)
• Harris Teeter Voluntarily Recalls Harris Teeter Frozen Organic Corn and Harris Teeter Frozen Mixed Vegetables, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - PharMEDium Sterile Preparations Compounded With a Single Recalled Lot of Fresenius Kabi Sensorcaine-MPF (bupivacaine HCl): Recall - Presence of Glass Particulate Matter, FDA MedWatch
• Updated: Watts Brothers Farms Organic Mixed Vegetables, Organic Super Sweet Corn, And Organic Peas And Trader Joe's Organic Super Sweet Corn Recalled Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• PharMEDium Issues Voluntary Nationwide Recall Sterile Preparations Compounded With a Single Recalled Lot of Fresenius Kabi Sensorcaine-MPF (bupivacaine HCl) Due to the Presence of Glass Particulate Matter, U.S. Food & Drug Administration (FDA)
• Tasty Toppings Recalls Dorothy Lynch Home Style Dressing, U.S. Food & Drug Administration (FDA)
• Twin City Foods, Inc. Recalls Frozen Organic Peas And Mixed Vegetables Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Stahlbush Island Farms, Inc. Recalls IQF Green Beans Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Voluntary Recall On Pulmuone Noodles, U.S. Food & Drug Administration (FDA)
• Schulze and Burch Biscuit Co. Recalls Various Millville Protein Chewy Bars Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Wheatberry Salad, U.S. Food & Drug Administration (FDA)
• Creative Snacks Co. Issues Recall on Sunflower Seeds and Trail Mixes Including Sunflower Seeds, U.S. Food & Drug Administration (FDA)
• The May 2016 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Three Public Meetings on FSMA, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Three Public Meetings on FSMA, U.S. Food & Drug Administration (FDA)
• Watts Brothers Farms Organic Mixed Vegetables, Organic Super Sweet Corn, And Organic Peas And Trader Joe's Organic Super Sweet Corn Recalled Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Releases 2014 Health and Diet Survey Findings, U.S. Food & Drug Administration (FDA)
• TreeHouse Foods Issues Voluntary Product Recall Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Pita Pal Foods, LP Recalls Corn Relish Salad, Texas Caviar Salad, Mediterranean 3 Bean Salad And Chipotle Quinoa Salad Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• TreeHouse Foods Amends Product Recall Information, U.S. Food & Drug Administration (FDA)
• Hickory Harvest Recalls Certain Sunflower Kernel Products Because Of Possible Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Updated: CRF Frozen Foods Expands Voluntary Recall to Include All Frozen Vegetable and Fruit Products Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Brown & Haley Issues Voluntary Recall of Mountain Thins "Trail Mix" Flavor Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Giant Eagle Voluntarily Recalls Bulk Sunflower Seeds Sold at Pittsburgh Market District Stores, U.S. Food & Drug Administration (FDA)
• Giant Eagle Voluntarily Recalls Bulk Sunflower Seeds Sold at Ohio Market District Stores, U.S. Food & Drug Administration (FDA)
• Market District Voluntarily Recalls Bulk Sunflower Seeds, U.S. Food & Drug Administration (FDA)
• Kroger Recalls Sunflower Products after Supplier Listeria Concern, U.S. Food & Drug Administration (FDA)
• Giant Eagle Voluntarily Recalls Bulk Sunflower Seeds Sold at Select Giant Eagle and Market District Stores, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: B. Braun Medical Inc. Recalls Dialog+ Hemodialysis Systems Due Defective Conductivity Sensors, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Recognizes Canada as Having a Comparable Food Safety System to the U.S., U.S. Food & Drug Administration (FDA)
• Frontera Foods Issues Allergy Alert for Undeclared Soy Allergen in Original Taco Skillet Sauce with a "Best By" Date of "13 Apr 17", U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Frontera Foods Issues Allergy Alert for Undeclared Soy Allergen in Original Taco Skillet Sauce with a "Best By" Date of "13 Apr 17", U.S. Food & Drug Administration (FDA)
• Recall of Certain Sunflower Kernel Products Due to Possible Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals May 2016 Update, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Dialog+ Hemodialysis Systems by B. Braun Medical: Class I Recall - Defective Conductivity Sensors, FDA MedWatch
• Blue Bell Ice Cream Recalls Mispackaged Rocky Road Pints That Contain Cookies 'N Cream Ice Cream; Potential Allergy Concerns For Those With Wheat and Soy Allergies, U.S. Food & Drug Administration (FDA)
• Cook Medical Issues Global, Voluntary Recall of Catheters with Beacon Tip Technology, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Beacon Tip Technology Catheters by Cook Medical: Recall - Polymer Degradation of the Catheter Tip, FDA MedWatch
• FDA publishes revised draft guidance for developing direct-acting antiviral drugs for treatment of chronic hep C, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Transfers Siluriformes Fish Inspection to USDA, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Aripiprazole (Abilify, Abilify Maintena, Aristada): Drug Safety Communication - FDA Warns About New Impulse-control Problems, FDA MedWatch
• CRF Frozen Foods Expands Voluntary Recall to Include All Frozen Vegetable and Fruit Products Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Vitalicious Issues Allergy Alert For Undeclared Milk In SELECT Apple Crumb VitaTops, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Brintellix (vortioxetine): Drug Safety Communication - Brand Name Change to Trintellix, to Avoid Confusion With Antiplatelet Drug Brilinta (ticagrelor), FDA MedWatch
• Giant Eagle Voluntarily Recalls Walnut Delight and Pecan Tassie Cookies Due to an Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• CSM Bakery Solutions Voluntary Recalls 8" Single Layer Red Velvet Cake Sold At Safeway And 12” Decorated Chocolate Chip Cookie Sold At Acme And Jewel Stores Due To Undeclared Peanut Allergen, U.S. Food & Drug Administration (FDA)
• CSM Bakery Solutions' Voluntary Recall of Cinnabon Stix® Due to Undeclared Peanut Allergen, U.S. Food & Drug Administration (FDA)
• FDA launches public education campaign to prevent and reduce tobacco use among LGBT young adults, U.S. Food & Drug Administration (FDA)
• The Republic of Tea Issues Voluntary Recall of Organic Turmeric Ginger Green Tea, U.S. Food & Drug Administration (FDA)
• 7-Eleven Issues Allergy Alert on Undeclared Peanut in Fresh Fully Baked Chocolate Chunk, Sugar and Oatmeal Raisin Cookies, U.S. Food & Drug Administration (FDA)
• Bakery Express of Central FL., Inc. Issues Alleregy Alert on Undeclared Peanuts in 7-Eleven Fresh to Go Cookies, U.S. Food & Drug Administration (FDA)
• Making It A Lifestyle, L.L.C. Issues a Voluntary Nationwide Recall of 3rd Degree, Black Gold X Advanced, and Black Label X Due to the Presence of Undeclared Sibutramine and Sildenafil, U.S. Food & Drug Administration (FDA)
• World's Choice Products, Inc. Issues Allergy Alert on Undeclared Milk And Soy Lecithin From Whey Protein in Supreme Elixir, Kids Juice, And Xtreme Fiber Detox, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - May 2, 2016, U.S. Food & Drug Administration (FDA)
• 7 Things to Know About Arsenic in Rice & Rice Cereal, FoodSafety.gov
• CFSAN Constituent Update - Final Guidance on Menu Labeling, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Releases Guide on Pet Food Diets Intended to Treat Diseases, U.S. Food & Drug Administration (FDA)
• Southeastern Grocers Issues Voluntary Recall on Undeclared Peanuts in Bakery Creme Cakes, U.S. Food & Drug Administration (FDA)
• Old Home Kitchens Issues Allergy Alert and Voluntary Recall on Undeclared Peanuts in "Old Home Kitchens 14oz Sliced Creme Cake", U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA NARMS Retail Meat Interim Report for Salmonella Shows Encouraging Early Trends Continue, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Public Meetings on Implementation of the FSMA Prevention-Oriented Import Safety Programs, U.S. Food & Drug Administration (FDA)
• Bakery Express of Southern California Issues Allergy Alert on Undeclared Peanut in 7-Eleven Fresh To Go Cookies, U.S. Food & Drug Administration (FDA)
• Schaffner Distributing Pronutri LLC. Issues an Allergy Alert on Undeclared Soy Lecithin and Milk in Re-VITA-lize, U.S. Food & Drug Administration (FDA)
• Fresenius Kabi Issues Voluntary Nationwide Recall of Sensorcaine®-MPF (bupivacaine HCl) Injection, USP due to the Presence of Particulate Matter Characterized as Glass, U.S. Food & Drug Administration (FDA)
• CSM Bakery Solutions Issues Allergy Alert on Undeclared Peanut in Chick-Fil-A Chocolate Chunk Cookies, U.S. Food & Drug Administration (FDA)
• Krasnyi Oktyabr USA Inc. Recalls Vobla (Roach) Dry Eviscerated Salted Fish and Bream Dry Eviscerated Salted Fish Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Glenn Wayne Wholesale Bakery Issues Allergy Alert on Undeclared Peanuts in Select 7-Eleven Fresh To Go Cookies, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sensorcaine-MPF (bupivacaine HCl) by Fresenius Kabi: Recall - Presence of Particulate Matter, FDA MedWatch
• Protect Your Baby from Cronobacter Infection, FoodSafety.gov
• FDA MedWatch - Fluconazole (Diflucan): Drug Safety Communication - FDA Evaluating Study Examining Use of Oral Fluconazole (Diflucan) in Pregnancy, FDA MedWatch
• CVS Pharmacy Announces Voluntary Recall of Gold Emblem Abound Organic Spiced Herbal Tea Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CRF Frozen Foods Recalls Frozen Vegetables Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Nuvi Global Corporation Issues Allergy Alert on Undeclared Milk and Soy in StemVitae 30oz Liquid Multivitamin, U.S. Food & Drug Administration (FDA)
• FDA proposes ban on electrical stimulation devices intended to treat self-injurious or aggressive behavior, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Proposal to Ban Electrical Stimulating Devices (ESDs) for self-injurious or aggressive behavior, U.S. Food & Drug Administration (FDA)
• Celebrate Earth Day by Reducing Food Waste & Foodborne Illness, FoodSafety.gov
• Urgent Product Recall for Undeclared Soy and Milk Allergens, U.S. Food & Drug Administration (FDA)
• Pharmakon Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of All Sterile Compounded Products Due to FDA Concern of Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Exceptional Health Products Issues Allergy Alert On Undeclared Soy And Milk Allergens In Angel Wings - Daily Multi 120 Capsules, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Extended Comment Period Associated with Raw Manure as Fertilizer, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Covidien Oridion Labeled Capnostream 20 and Capnostream 20p Patient Monitor Battery Packs by Medtronic: Recall - Risk of Thermal Damage, FDA MedWatch
• Medtronic Announces Worldwide Voluntary Recall for Battery Pack In Covidien Oridion Labeled Capnostream20 and Capnostream20p Patient Monitors, U.S. Food & Drug Administration (FDA)
• Mary's Home Canning Recalls Mary's Home Made Vegetable Soup Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Back to Nature Expands Voluntary Recall for Limited Number of Classic Creme Cookies Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Boston Scientific Corporation Recalls Fetch 2 Aspiration Catheter Due to Shaft Breakage, U.S. Food & Drug Administration (FDA)
• FDA launches first ad campaign focused on dangers of smokeless tobacco among rural teens, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Final Guidance for Industry #231 Available – Distributor Labeling for New Animal Drugs, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Public Meeting in Preparation for ICCR-10, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces 2016 Public Meetings and Comment Period on Reauthorization of Two Animal Drug User Fee Programs, U.S. Food & Drug Administration (FDA)
• Midwest International Corp Issues Allergy Alert on Undeclared Milk in Hosdo Cake, U.S. Food & Drug Administration (FDA)
• Milky Way International Trading Corp. Issues Voluntary Nationwide Recall of Nice! Peach Slices and Nice! Mixed Fruits in 8-ounce Glass Jars Due to Possible Glass in Products, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Issues Import Alert on Imported Shrimp and Prawns from Peninsular Malaysia, U.S. Food & Drug Administration (FDA)
• A&S Food Trading Inc. Issues Alert on Undeclared Sulfites in Gorgeous Memory Daylily, U.S. Food & Drug Administration (FDA)
• Thomas Star Bakery of Ohio LLC Issues Voluntary Recall on Buns Bread, U.S. Food & Drug Administration (FDA)
• Ryszard Food Distributor Inc. Issues Alert on Undeclared Sulfites in Novus Snack Golden Raisins in 10 ounce plastic packages, U.S. Food & Drug Administration (FDA)
• Sterile Drug Products from Pharmakon Pharmaceuticals, Inc: CDER Statement - FDA alerts health care professionals not to use due to a lack of sterility assurance and other quality issues, FDA MedWatch
• OLMA-XXI, Inc. Recalls Norven Herring in Oil Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - March 2016 Drug Safety Labeling Changes - 35 products with revisions to Prescribing Information, FDA MedWatch
• Sugarfina Issues Allergy Alert on Undeclared Peanuts in Milk Chocolate Malt Balls, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 50% Magnesium Sulfate Injection, USP by Hospira: Recall - Presence Of Particulate Matter, FDA MedWatch
• Nubreed Nutrition Issues a Voluntary Nationwide Recall of Undisputed, a Product Marketed as a Dietary Supplement Containing Acacia Rigidula, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Issues Final Guidance on Exempt Infant Formula Production, U.S. Food & Drug Administration (FDA)
• FDA approves folic acid fortification of corn masa flour, U.S. Food & Drug Administration (FDA)
• Hospira Issues A Voluntary Recall For One Lot Of 50% Magnesium Sulfate Injection, USP Due To The Presence Of Particulate, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Focus Diagnostics Laboratory Examination Kits: Class I Recall - Inaccurate Test Results, FDA MedWatch
• Medical Device Safety and Recalls: Focus Diagnostics Recalls Laboratory Examination Kits Due to Inaccurate Test Results, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Vascular Solutions Recalls Guardian II Hemostasis Valve Due to Low Pressure Seal Defect, U.S. Food & Drug Administration (FDA)
• Enforcement Report 4/13/2016, U.S. Food & Drug Administration (FDA)
• Country Favor Issues Allergy Alert on Undeclared Peanuts in "Best Taste Keo Me Den Candy", U.S. Food & Drug Administration (FDA)
• EBB (U.S.) Inc. (English Bay Batter) Issues Voluntary Allergy Alert for PICs by Price Chopper Cinnamon Rolls with Cream Cheese Icing due to Incorrect Allergen Caution, U.S. Food & Drug Administration (FDA)
• Reser's Fine Foods, Inc. Recalls Refrigerated Salads Because of Possible Health Risk Due to Onion Supplier Recall, U.S. Food & Drug Administration (FDA)
• Back to Nature Issues Allergy Alert for Limited Number of Classic Creme Cookies Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Mislabeled Asparagus, Pea and Ricotta Salad Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• Dexcom, Inc., Issues Press Release to Supplement Previous Customer Notification, U.S. Food & Drug Administration (FDA)
• Super Herbs Issues Voluntary Nationwide Recall Of SUPER HERBS Due To Presence Of Undeclared Sibutramine, Desmethylsibutramine and/or Phenolphthalein, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Dexcom Inc. Recalls G4 Platinum and G5 Mobile Continuous Glucose Monitoring System Receivers Due to Audible Alarm Failure, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fetch 2 Aspiration Catheter by Boston Scientific: Recall - Shaft Breakage, FDA MedWatch
• FDA MedWatch - G4 Platinum and G5 Mobile Continuous Glucose Monitoring System Receivers by Dexcom.: Class I Recall - Audible Alarm Failure, FDA MedWatch
• Voluntary Recall of Fetch 2 Aspiration Catheter, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Guardian II Hemostasis Valves by Vascular Solutions, Inc: Recall - Risk of Air Leakage, FDA MedWatch
• FDA approves new drug for chronic lymphocytic leukemia in patients with a specific chromosomal abnormality, U.S. Food & Drug Administration (FDA)
• Vascular Solutions, Inc. Issues Recall of Guardian® II Hemostasis Valves, U.S. Food & Drug Administration (FDA)
• Read about Minority Women's Health and more, FDA Office of Women's Health
• Progressive Gourment Inc. Issues an Allergy Alert on Taste of Inspirations Edamame Rangoon Due to Possible Mislabeling and Undeclared Crustacean Shellfish, U.S. Food & Drug Administration (FDA)
• FDA takes steps to withdraw approval of the swine drug carbadox due to safety concerns, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Metformin-containing Drugs: Drug Safety Communication - Revised Warnings for Certain Patients With Reduced Kidney Function, FDA MedWatch
• Michel Et Augustin Inc. Issues Allergy Alert on Undeclared Hazelnuts in Petites Baguettes Butter Cookies Dark Chocolate, U.S. Food & Drug Administration (FDA)
• 2016 World Health Day - Food Safety & Diabetes, FoodSafety.gov
• WD Import and Export Inc. Issues an Alert on Dried Fish Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA allows marketing of first-of-kind tissue containment system for use with certain laparoscopic power morcellators in select patients, U.S. Food & Drug Administration (FDA)
• The April 2016 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• CVM Updates - Comment Period on draft EA and preliminary FONSI for Genetically Engineered Mosquitoes Extended, U.S. Food & Drug Administration (FDA)
• 4/6/2016 Enforcement Report, U.S. Food & Drug Administration (FDA)
• Granna’s LLC Issues Allergy Alert On Undeclared Milk in French Toast, U.S. Food & Drug Administration (FDA)
• FDA approves first leadless pacemaker to treat heart rhythm disorders, U.S. Food & Drug Administration (FDA)
• Fresh From Texas Recalls Apple Product Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Supports Mini-Symposium about Blackhead Disease Organized by AAAP, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals April 2016 Update (Green Book), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Diabetes Medications Containing Saxagliptin and Alogliptin: Drug Safety Communication - Risk of Heart Failure, FDA MedWatch
• FDA MedWatch - Continuum Labs LGD-4033 by Invisiblu International: Recall - Investigational Drug Not Approved for Use, FDA MedWatch
• HIV/AIDS Update - Approval of Descovy (emtricitabine (FTC) and tenofovir alafenamide (TAF) fixed-dose combination), U.S. Food & Drug Administration (FDA)
• INVISIBLU International LLC Issues Voluntary Nationwide Recall Of Continuum Labs Lgd-4033 Due To Product Containing LGD-4033 (Ligandrol), An Investigational Drug Not Approved For Use, U.S. Food & Drug Administration (FDA)
• FDA releases final rule to ensure food safety during transport, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Final Rule to Ensure Food Safety During Transport, U.S. Food & Drug Administration (FDA)
• Sports Fans Against Foodborne Illness, FoodSafety.gov
• Snyder's-Lance Announces Voluntary Recall of a Limited Number of Emerald Cashew Roasted Salted Halves & Pieces Due to Potential Presence of Glass, U.S. Food & Drug Administration (FDA)
• Alimentos Congelados, S.A. Recalls Frozen Broccoli Cuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Roland Foods, LLC, Initiates A Voluntary Recall Of Roland Fire Roasted Red Pepper Strips Due To The Possible Presence Of Glass In The Product, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sterile Drug Products by Medaus Pharmacy: FDA Alert - Lack of Sterility Assurance, FDA MedWatch
• FDA MedWatch - Urogynecologic Surgical Mesh Implants by Boston Scientific: Notification – Potential for Counterfeit Raw Material, FDA MedWatch
• CFSAN Constituent Update - FDA Proposes Limit for Inorganic Arsenic in Infant Rice Cereal, U.S. Food & Drug Administration (FDA)
• 7 Things Pregnant Women and Parents Need to Know About Arsenic in Rice and Rice Cereal, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Interference between Computed Tomography (CT) and Electronic Medical Devices: Notification – Current Understanding of Potential Risk, FDA MedWatch
• Update of CVM's What's New - Final Guidance for Industry 156 Available, U.S. Food & Drug Administration (FDA)
• Lee Seed Company, Inc. Issues Allergy Alert on Undeclared Milk in Yogurt Super Soynuts, U.S. Food & Drug Administration (FDA)
• Food Bank Recalls Canned Mandarin Oranges Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• R.W. Baker Co. Issues Allergy Alert on Undeclared Peanuts in "Meijer Plain Knot Rolls" "Assorted Dinner Rolls 128 ct.", U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Updated Information on Interference between CT and Electronic Medical Devices, U.S. Food & Drug Administration (FDA)
• Flowers Foods Issues Allergy Alert and Voluntary Recall on Cobblestone Bread Co. Wheat English Muffins in CT, DE, KY, ME, MD, MA, NH, NJ, NY, NC, OH, PA, RI, SC, TN, VT, VA, DC, and WV, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update -Correction:Truvada (emtricitabine/tenofovir disoproxil fumarate) pediatric labeling expanded, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Cook Medical Recalls Central Venous Catheter and Pressure Monitoring Sets and Trays due to Tips that May Split or Separate, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: The FDA Recommends Against Using OxySure Portable Emergency Oxygen System, Model 615: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Enforcement Report, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 5% Dextrose Injection USP in PAB Container by B. Braun Medical: Recall - Leakage and/or Particulate Matter, FDA MedWatch
• CVM Updates - FDA and Health Canada announce first simultaneous review and approval of a veterinary drug for food-producing animals, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - OxySure Portable Emergency Oxygen System, Model 615 by OxySure Therapeutics, Inc: FDA Safety Communication - Do Not Use, FDA MedWatch
• B. Braun Medical Inc. Issues Voluntary Nationwide Recall of Lot J5J706, 5% Dextrose Injection USP in PAB Container Due to Leakage and/or Particulate Matter Identified To Be Microbial Growth, U.S. Food & Drug Administration (FDA)
• Revised Press Release For: "Reliable Drug" Recall of all Compounded Medications Due to a Potential for Mislabeling and Lack of Quality Assurance, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Revised Press Release For: "Reliable Drug" Recall of all Compounded Medications Due to a Potential for Mislabeling and Lack of Quality Assurance, U.S. Food & Drug Administration (FDA)
• QFC Issues Allergy Alert on Undeclared Pecans, Wheat, and Soy in Cranberry Chicken Salad, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Compounded Products by Reliable Drug Pharmacy: Recall - Potential for Mislabeling and Lack of Quality Assurance, FDA MedWatch
• Trader Joe's Issues Voluntary Allergy Alert on Undeclared Milk in Chocolate Orange Sticks and Chocolate Raspberry Sticks, U.S. Food & Drug Administration (FDA)
• "Reliable Drug" Recalls All Compounded Medications Due to a Potential for Mislabeling and Lack of Quality Assurance, U.S. Food & Drug Administration (FDA)
• Smallbatch Pets Inc. Voluntarily Recalls Frozen Dog Duckbatch Sliders Due to Possible Salmonella and Listeria Monocytogenes Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Truvada (emtricitabine/tenofovir disoproxil fumarate) pediatric labeling expanded, & additional tablet strengths added, U.S. Food & Drug Administration (FDA)
• American Gourmet Recalls American Gourmet Roasted/Salted Pistachios Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Gerber is Voluntarily Recalling Two Batches of GERBER® Organic 2ND FOODS® Pouches Due to a Packaging Defect That May Result in Product Spoilage, U.S. Food & Drug Administration (FDA)
• AA USA Trading Inc. Issues Allergy Alert on Undeclared Sulfites in AA Brand Dried Ginger Slice, U.S. Food & Drug Administration (FDA)
• FDA takes important step to increase the development of, and access to, abuse-deterrent opioids, U.S. Food & Drug Administration (FDA)
• Enforcement Report 3/23/2016, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Best Bentonite Clay by Best Bentonite: FDA Alert - Risk of Lead Poisoning, FDA MedWatch
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update: Warning Letters Address Drug Claims Made for Products Marketed as Cosmetics, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update: Warning Letters Address Drug Claims Made for Products Marketed as Cosmetics, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update: Warning Letters Address Drug Claims Made for Products Marketed as Cosmetics, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Opioid Pain Medicines: Drug Safety Communication - New Safety Warnings Added to Prescription Opioid Medications, FDA MedWatch
• FDA warns about several safety issues with opioid pain medicines; requires label changes, U.S. Food & Drug Administration (FDA)
• NOW Health Group, Inc. Voluntarily Recalls Limited Quantity of Six Dietary Supplements Due to Mislabeling, U.S. Food & Drug Administration (FDA)
• Proposal to Ban Powdered Surgeon’s Gloves, Powdered Patient Examination Gloves, and Absorbable Powder for Lubricating a Surgeon’s Glove, U.S. Food & Drug Administration (FDA)
• H-E-B Issues Voluntary Recall: Select 5oz Hill Country Fare Chunk Light Tuna in Oil Recalled for Potential Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sodium Bicarbonate Injection, USP by Hospira: Recall - Particulate Matter, FDA MedWatch
• FDA proposes ban on most powdered medical gloves, U.S. Food & Drug Administration (FDA)
• FDA approves new treatment for inhalation anthrax, U.S. Food & Drug Administration (FDA)
• Hospira Issues a Voluntary Recall for One Lot of Sodium Bicarbonate Injection, USP Due to the Presence of a Particulate, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - MFA Incorporated issues recall on rabbit feed pellets (both bagged and bulk) in southwest Missouri due to excessive sodium, U.S. Food & Drug Administration (FDA)
• MFA Incorporated issues recall on rabbit feed pellets (both bagged and bulk) in southwest Missouri due to excessive sodium, U.S. Food & Drug Administration (FDA)
• UPDATE - Ashland Food Co-Op Recalls Organic Raw Macadamia Nuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GlideScope Titanium Single-Use Video Laryngoscope by Verathon: Class I Recall - Potential Video Feed Disruption, FDA MedWatch
• Medical Device Safety and Recalls: Verathon Inc. Recalls GlideScope Titanium Single-Use Video Laryngoscope Due to Potential Video Feed Disruption, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Arrow International Inc. Recalls Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits Due to Sheath Separation Issue, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Funding Opportunity for States, U.S. Food & Drug Administration (FDA)
• Tri-Union Seafoods LLC Issues Precautionary, Voluntary Recall on Select 5 oz. Canned Chunk Light Tuna in Oil and 5 oz. Canned Chuck Light Tuna in Water, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Final Rule on Bovine Spongiform Encephalopathy, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: FDA Announces Final Rule on Bovine Spongiform Encephalopathy, U.S. Food & Drug Administration (FDA)
• Bumble Bee Foods, LLC Issues Voluntary Recall on 3 Production Codes of Canned Chunk Light Tuna Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Organic Raw Macadamia Nuts Recalled Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Draft Guidance for Industry Available, U.S. Food & Drug Administration (FDA)
• Enforcement Report 3/16/2016, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Olympus Validates Updated Reprocessing Instructions for Duodenoscope Models TJF-160F and TJF-160VF: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Grant Award Opportunity for Antimicrobial Use and Resistance Data Collection, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Eye Drops: FDA Statement - Potential Risk of Loose Safety Seals, FDA MedWatch
• Medical Device Safety and Recalls: Abbott Vascular Recalls MitraClip Clip Delivery System Due to Issue with Delivery System Deployment Process, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Duodenoscope Models TJF-160F and TJF-160VF by Olympus: Safety Communication - Reprocessing Instructions Validated, FDA MedWatch
• Texas Star Nut & Food Company is Expanding the Recall on Natural Pistachio Kernels and Products Containing Pistachio Kernels, Which Were Previously Voluntarily Recalled Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA's New Online "Snack Shack" in Whyville Teaches Youth about the Nutrition Facts Label, U.S. Food & Drug Administration (FDA)
• FDA Enforcement Report Update, U.S. Food & Drug Administration (FDA)
• Northern Tier Bakery LLC Issues Voluntary Recall Due to Allergy Alert on Undeclared Milk in Tuna Salad Wedge Sandwich, U.S. Food & Drug Administration (FDA)
• Awareness Voluntary Recalls Boost Tea Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - February 2016 Drug Safety Labeling Changes includes 21 products with revisions to Prescribing Information., FDA MedWatch
• Update of CVM's What's New - Updated Medicated Feed Mill Licenses/VFD Distributor Notifications, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Arrow International Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits by Teleflex Incorporated : Class I Recall - Sheath Body may become Separated from Sheath Hub, FDA MedWatch
• Kanan Enterprises Conducts Nationwide Voluntary Recall of Natural in Shell Pistachios, U.S. Food & Drug Administration (FDA)
• Teleflex Incorporated Announces Worldwide Recall of ARROW International Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits, U.S. Food & Drug Administration (FDA)
• JRZ Dairy, Inc., Selinsgrove, PA Recalls Whole Milk Yogurt and Low Fat Yogurt Because of a Possible Health Risk Due To Incomplete Pasteurization, U.S. Food & Drug Administration (FDA)
• Nestlé USA Announces Voluntary Recall of a Limited Number of DiGiorno® Pizzas, Lean Cuisine® and Stouffer’s® Products Due to the Potential Presence of Foreign Material, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Comment Period for Draft Environmental Assessment for Genetically Engineered Mosquito, U.S. Food & Drug Administration (FDA)
• Texas Star Nut and Food Co., Inc. Voluntarily Recalls Nature's Eats, Natural Pistachio Kernels Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Best Cash & Carry Inc. Issues Alert on Undeclared Sulfites in Apricots, U.S. Food & Drug Administration (FDA)
• Teva Pharmaceuticals Initiates Voluntary Nationwide Recall of One Lot of Amikacin Sulfate Injection USP 1 gram/4mL (250 mg/mL) Vials Due to Glass Particulate Matter, U.S. Food & Drug Administration (FDA)
• Best Cash & Carry Inc. Issues Allert on Undelared Sulfites in Apricots, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA’s Antimicrobial Resistance Monitoring Team Wins Government Award to Design Public Health Surveillance Mobile App, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Amikacin Sulfate Injection USP, 1 gram/4mL (250 mg/mL) Vials by Teva: Recall - Glass Particulate Matter, FDA MedWatch
• Read about Women's Health Research, Essure, HIV and more, FDA Office of Women's Health
• CFSAN Constituent Update: FDA Issues Final Guidance for Industry on How to Reduce Acrylamide in Certain Foods, U.S. Food & Drug Administration (FDA)
• Wonderful Pistachios Voluntarily Recalls Pistachios Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Wonderful Pistachios Voluntarily Recalls Pistachios Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Human and Animal Sterile Drug Products by I.V. Specialty: FDA Alert - Lack of Sterility Assurance, FDA MedWatch
• CFSAN Constituent Update - Menu Labeling Enforcement, U.S. Food & Drug Administration (FDA)
• Antes de adquirir un producto o contratar un servicio, vea estos videos, GobiernoUSA.gov
• Eatin' Alive Issues Allergy Alert on Undeclared Soy in Thai Peanut Noodles and Thai Wrap, U.S. Food & Drug Administration (FDA)
• CVM Updates - Changes in Leadership for FDA's Foods and Veterinary Medicine Program, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Changes in Leadership for FDA's Foods and Veterinary Medicine Program, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Final Guidance for Industry 203 Available - Ensuring Safety of Animal Feed Maintained and Fed On-Farm, U.S. Food & Drug Administration (FDA)
• Specialty Commodities, Inc. Issues Allergy Alert on Undeclared Cashew Allergen in Dry Roasted Almonds, U.S. Food & Drug Administration (FDA)
• ¡Celebremos el “Mes de la historia de la mujer”!, GobiernoUSA.gov
• Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of Fluconazole Injection, USP, (in 0.9% Sodium Chloride) 200mg per 100ml Due to the Discovery of an Out of Specification Impurity Result Detected During Routine Quality Testing of Stability Samples at the 18-Month Interval, U.S. Food & Drug Administration (FDA)
• Voluntary Recall of Cheese and Fruit Bistro Box for Undisclosed Allergen, U.S. Food & Drug Administration (FDA)
• Voluntary Recall of Non Organic Gogo Squeez Applesauce Pouches, U.S. Food & Drug Administration (FDA)
• Progressive Gourment Inc. Issues Alert on Sausage Egg Cheese Muffin Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fluconazole Injection, USP, (in 0.9 Percent Sodium Chloride) 200mg per 100ml: Recall - Elevated Impurity, FDA MedWatch
• Enforcement Report for March 02, 2016, U.S. Food & Drug Administration (FDA)
• Maytag Dairy Farms Blue Cheese Sold at 17 Select Schnuck Markets Recalled Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Loki Fish Company Recalls Smoked Pink Salmon Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• BI-LO Store in Glennville, GA Recalls Cantaloupes Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Obtenga ayuda tributaria en español, GobiernoUSA.gov
• Medical Device Safety and Recalls: Dräger Evita V500 and Babylog VN500 Ventilators - Recall Expanded to Include Optional PS500 Batteries with New Power Supply Firmware, U.S. Food & Drug Administration (FDA)
• Hy-Vee Voluntarily Recalls Maytag Blue Cheese Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA and DOJ take action against Virginia soybean business for selling contaminated sprouts, U.S. Food & Drug Administration (FDA)
• Ayude a prevenir la tos ferina en los bebés, GobiernoUSA.gov
• CFSAN Constituent Update - FDA Seeks Public Comments, Data and Information on Assessing the Risk of Raw Manure as Fertilizer, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals March 2016 Update (Green Book), U.S. Food & Drug Administration (FDA)
• FDA Investigates Multistate Outbreak of Salmonella Muenchen Linked to Alfalfa Sprouts Produced by Sweetwater Farms, U.S. Food & Drug Administration (FDA)
• COMPLERA label updated, U.S. Food & Drug Administration (FDA)
• ODEFSEY fixed dose approved, U.S. Food & Drug Administration (FDA)
• STRIBILD label updated, U.S. Food & Drug Administration (FDA)
• Olysio label revised, U.S. Food & Drug Administration (FDA)
• CVM Updates - NARMS Announces Grant Award Opportunity for Retail Meat Testing in the National Antimicrobial Resistance Monitoring System (NARMS), U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Maytag Blue Cheese Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Jack and the Green Sprouts, Inc. is Voluntarily Recalling Alfalfa and Alfalfa Onion Sprouts, U.S. Food & Drug Administration (FDA)
• FDA Takes Additional Action to Better Understand Safety of Essure, U.S. Food & Drug Administration (FDA)
• FDA takes additional action to better understand safety of Essure, inform patients of potential risks, FDA Office of Women's Health
  • <Possible follow-ups>
  • FDA takes additional action to better understand safety of Essure, inform patients of potential risks, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - MitraClip Delivery System by Abbott: Safety Notice - Reinforcement of Proper Procedures to Operate and Deploy, FDA MedWatch
• CVM Updates - CVM Director Dunham to Leave Agency for New Opportunity in Academia, U.S. Food & Drug Administration (FDA)
• Maytag Dairy Farms Expands Voluntary Recall Of Blue Cheese Products Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Abbott Issues Voluntary Safety Notice on MitraClip Delivery System Deployment Process, U.S. Food & Drug Administration (FDA)
• FDA providing $2 million in new grants for natural history studies in rare diseases, U.S. Food & Drug Administration (FDA)
• Temporada electoral: participe en nuestra sesión de preguntas el 29 de febrero, GobiernoUSA.gov
• Federal judge approves consent decree with Florida dietary supplement distributor, Viruxo, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Questions and Answers on Spice Safety, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Cook Medical Expands Recall for Beacon Tip Angiographic Catheters to Include Additional Product Lots, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 24, 2016, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New FDA Commissioner, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Neurosurgical Head Holders (Skull Clamps) : FDA Safety Communication - Device Slippage, FDA MedWatch
• Medical Device Safety and Recalls: Neurosurgical Head Holders (Skull Clamps) and Device Slippage: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update: Cosmetics Program; Import and Domestic, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Holding Public Meeting on FSMA Prevention-Oriented Import System Regulations and Implementation, U.S. Food & Drug Administration (FDA)
• Lipari Foods Issues Allergy Alert on Dark Chocolate Covered Coffee Bean Products Due to Undeclared Almonds, U.S. Food & Drug Administration (FDA)
• Rucker's Wholesale & Service Co. Issues Allergy Alert on Undeclared Peanut Ingredient in Uncle Bucks & Cabela's Classic Candies Maple Nut Candy Peg Bags, U.S. Food & Drug Administration (FDA)
• Marathon Ventures, Incorporated Announces Voluntary Recall of Raw Macadamia Nuts Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Updated - FDA Recommends Health Care Facilities Transition from Custom Ultrasonics Endoscope Washer/Disinfectors to Alternate Reprocessing Methods: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update: Pakco (Pty) Ltd., U.S. Food & Drug Administration (FDA)
• Wilderness Family Naturals Issues Allergy Alert on Undeclared Milk in Organic Coconut Milk Powder And Products Containing Organic Coconut Milk Powder, U.S. Food & Drug Administration (FDA)
• Best Foods Inc. Issues Allergy Alert on Undeclared Peanuts in Deer Brand Cumin Powder 7 Ounce and Deer Brand Cumin Powder 14 Ounce, U.S. Food & Drug Administration (FDA)
• Información importante antes de presentar su declaración de impuestos, GobiernoUSA.gov
• Participe mañana en nuestra charla bilingüe sobre el proceso electoral y de primarias, GobiernoUSA.gov
• CFSAN Constituent Update - President’s FY 2017 Budget Requests FSMA Investments, U.S. Food & Drug Administration (FDA)
• Maytag Dairy Farms Issues Voluntary Recall of Blue Cheese Due to Food Safety Concern, U.S. Food & Drug Administration (FDA)
• Maytag Dairy Farms Expands Voluntary Recall of Blue Cheese Due to Food Safety Concern, U.S. Food & Drug Administration (FDA)
• Maytag Dairy Farms Voluntarily Recalls Blue Cheese Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Small Entity Compliance Guide on Omega-3 Fatty Acids Final Rule, U.S. Food & Drug Administration (FDA)
• Fresh Creative Foods Issues Allergy Alert on Undeclared Fish (Anchovy) in H-E-B Tartar Sauce, U.S. Food & Drug Administration (FDA)
• Health Matters America Inc. Issues Nationwide Recall of Sprouted Flax Seed Powder and Sprouted Chia & Flax Seed Powder Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 17, 2016, U.S. Food & Drug Administration (FDA)
• Country Life Natural Foods Recalls Raw Pistachios Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Wild Blue Yonder Foods Issues Recall for Chappaqua Crunch Granola with Blueberries and Bananas Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Hypothyroidism in Dogs—There’s now an FDA-Approved Treatment, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - ED-3490TK Video Duodenoscope by Pentax: FDA Safety Communication - Pentax Validates Reprocessing Instructions, FDA MedWatch
• Peking Food LLC Issues Allergy Alert For Undeclared Egg in Assorted Chef Hon Brand Steamed Buns, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: PENTAX Validates Reprocessing Instructions for ED-3490TK Video Duodenoscopes: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 0.9 Percent Sodium Chloride Solution for Irrigation by Baxter: Recall - Presence of Particulate Matter, FDA MedWatch
• CFSAN Constituent Update - FDA Announces Grant Award to Establish Regional Centers for Food Safety Training, Outreach and Technical Assistance, U.S. Food & Drug Administration (FDA)
• Baxter Issues Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Solution for Irrigation Due to Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• Get a Free Heart Health Kit for Women, FDA Office of Women's Health
• FDA Announces Pharmakon Pharmaceuticals Voluntary Recall of Morphine Sulfate 0.5 mg/mL Preservative Free in 0.9% Sodium Chloride, U.S. Food & Drug Administration (FDA)
• Lipari Foods Issues Voluntary Recall of Various Retail and Food Service Raw Pistachio Products Due to Potential Salmonella Risk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Lipari Foods Issues Voluntary Recall of Various Retail And Food Service Raw Pistachio Products Due to Potential Salmonella Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Morphine Sulfate 0.5 mg/mL Preservative Free in 0.9 percent Sodium Chloride by by Pharmakon Pharmaceuticals: Recall - Super-potent Product, FDA MedWatch
• Forever Cheese Recalls Imported Mitica Brand Pecorino Aged Cheese in Walnut Leaves For Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Pecorino Aged Cheese in Walnut Leaves in Two Stores Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Maine smoked fish company agrees to halt production of adulterated fish, U.S. Food & Drug Administration (FDA)
• International Foodsource, LLC Issues a Voluntary Recall of Various Raw Pistachios Products Due to Possible Salmonella Risk, U.S. Food & Drug Administration (FDA)
• Garden of Life Expands Voluntary Recall to Include Additional Lots of Raw Meal Products Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update -Important changes to Harvoni affecting several categories of patients, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA to Reopen Comment Period on Proposed Rule on Gluten-Free Labeling of Fermented and Hydrolyzed Foods, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - January 2016 Drug Safety Labeling Changes includes 26 products with revisions to Prescribing Information., FDA MedWatch
• Enforcement Report for February 10, 2016, U.S. Food & Drug Administration (FDA)
• Rosas y espinas: en este Día de San Valentín, dígale no al abuso, GobiernoUSA.gov
• King Soopers Recalls Gourmet Bread Pudding Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Cook Medical Issues Global Recall of Select Lots of Central Venous Catheters and Pressure Monitoring Sets and Trays, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Central Venous Catheters and Pressure Monitoring Sets and Trays by Cook Medical: Recall - Catheter Tip Fracture and/or Separation, FDA MedWatch
• FDA MedWatch - Syrspend SF and Syrspend SF Grape Suspending Agents by Fagron: FDA Alert - Microbial Contamination with Yeast, FDA MedWatch
• FDA MedWatch - Oxylog 2000 Plus, 3000, and 3000 Plus Emergency Transport Ventilators by Dräger Medical: Class I Recall - System Error May Lead to a Halt in Ventilation Therapy, FDA MedWatch
• Medical Device Safety and Recalls: Dräger Medical Inc. Emergency Transport Ventilators, U.S. Food & Drug Administration (FDA)
• FDA seeks $5.1 billion total for FY 2017, including funds to implement food safety law, improve medical product safety and quality, U.S. Food & Drug Administration (FDA)
• The February 2016 MedSun Newsletter is now available, U.S. Food & Drug Administration (FDA)
• Giant Eagle Voluntarily Recalls Japanese Hand Breaded Cod Fillets Due to an Undeclared Soy Allergen, U.S. Food & Drug Administration (FDA)
• Living Tree Community Foods Recalls Macadamia Nuts and Macadamia Butter Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: FDA Is Taking a New Look at Criteria for Raw Milk Cheese, U.S. Food & Drug Administration (FDA)
• Fresh Express Announces Precautionary Recall of a Limited Quantity of Chopped Romaine Salad Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• TF Foods Issues Allergy Alert on Undeclared Peanuts in Fried Bean Snack (Na-Pia-Jo), U.S. Food & Drug Administration (FDA)
• The Jel Sert Company Issues a Voluntary Recall of Margaritaville Banana Cream Pie Filling due to Possible Salmonella Risk, U.S. Food & Drug Administration (FDA)
• H-E-B Creamy Creations Caramel Pecan Turtle Ice Cream Voluntarily Recalled Due to Possible Foreign Material in the Product, U.S. Food & Drug Administration (FDA)
• Food Safety Player's Guide for Tomorrow's Game, FoodSafety.gov
• FDA Hepatitis Update - Changes to the Daklinza (daclatasvir) label expand indication, U.S. Food & Drug Administration (FDA)
• Read about Heart Health, Opioids and more in the February eUpdate, FDA Office of Women's Health
• BJ's Wholesale Club Announces Recall of Deli Meats Due to Undeclared Pistachios in Product, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Save the Date - FSMA Public Meeting, U.S. Food & Drug Administration (FDA)
• Mahina Mele Farms, LLC Expands Voluntary Recall of Macadamia Nut Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Un plan realista y efectivo para mantenerse en forma, GobiernoUSA.gov
• Califf, FDA top officials call for sweeping review of agency opioids policies, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 03, 2016, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 27, 2016, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals February 2016 Update (Green Book), U.S. Food & Drug Administration (FDA)
• European Natural Food & Trading Co. Inc. Issues Allergy Alert on Undeclared Sulfites in Product, U.S. Food & Drug Administration (FDA)
• Sign Up Before the Big Game!, FoodSafety.gov
• Usted podría tener glaucoma y no saberlo, GobiernoUSA.gov
• Update of CVM's What's New - 2016 Windows to Regulatory Research Internship Program is canceled, U.S. Food & Drug Administration (FDA)
• Braga Organic Farms Issues Voluntary Recall of Pistachios Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Susan Mayne’s First Year as Director of CFSAN, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: FDA Announces Funding Opportunities for Education, Training and Technical Assistance under the FDA Food Safety Modernization Act (FSMA), U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - February 1, 2016, U.S. Food & Drug Administration (FDA)
• Garden of Life, LLC Recalls Raw Meal Organic Shake & Meal Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Pink Bikini and Shorts on The Beach Dietary Supplements by Lucy's Weight Loss System: Recall - Undeclared Drug Ingredient, FDA MedWatch
• Lucy's Weight Loss System Issues Voluntary Nationwide Recall of Pink Bikini and Shorts on The Beach Dietary Supplements Due To Possible Undeclared Active Pharmaceutical Ingredient, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Approval of Zepatier for treatment of chronic hepatitis C genotypes 1 and 4, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Warning Letters to Manufacturers of Unapproved Levothyroxine Drugs for Hypothyroidism in Dogs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Bentonite Me Baby – Bentonite Clay by Alikay Naturals: Consumer Warning - Risk of Lead Poisoning, FDA MedWatch
• FDA MedWatch - Crema Piel De Seda (Silky Skin Cream) by Viansilk: Consumer Warning - Risk of Mercury Poisoning, FDA MedWatch
• Medical Device Safety and Recalls: Arkray Recalls SPOTCHEM II Test Strips Due to Inaccurate Blood Sugar Readings, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - SPOTCHEM II Test Strips by Arkray: Class I Recall - Inaccurate Blood Sugar Readings, FDA MedWatch
• FDA approves first drug to show survival benefit in liposarcoma, U.S. Food & Drug Administration (FDA)
• Figi's Issues Recall Alert on Mislabeled Marzipan, U.S. Food & Drug Administration (FDA)
• House of Flavors Issues Allergy Alert on Undeclared Pecans in Purple Cow Cookie Butter Ice Cream, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Thornhill Research Inc. Recalls MOVES Ventilator System Due to Battery Problem, U.S. Food & Drug Administration (FDA)
• FDA Classifies St. Jude Medical Field Action For 447 Of The Company’s Optisure High Voltage Leads As A Class 1 Advisory In The U.S., U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: St. Jude Medical Recalls Optisure Dual Coil Defibrillation Leads Due to Damage that May Prevent Patient Therapy, U.S. Food & Drug Administration (FDA)