FDA News Releases

• Date Index

• The March 2017 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Vulto Creamery Issues Voluntary Recall of All Soft, Wash-Rind Raw Milk Cheeses Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Vulto Creamery Issues Voluntary Recall of All Soft, Wash-Rind Raw Milk Cheeses Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Landies Candies Co. Inc. Issues Allergy Alert on Undeclared Peanuts on “WEGMANS MILK CHOCOLATE (BIG EAR BUNNY) SUCKER”, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals, U.S. Food & Drug Administration (FDA)
• The Soynut Butter Co Recalls I.M. Healthy Original Creamy Soynut Butter Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Evanger’s Pet Food and Against the Grain Voluntarily Recalls Additional Products Out of Abundance of Caution due to Potential Adulteration with Pentobarbital, U.S. Food & Drug Administration (FDA)
• Meijer Expands Recall To Include Meijer Artisan Made Natural Muenster Cheese And Pre-Made Ham Sub Sandwich Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Evanger’s Pet Food and Against the Grain Voluntarily Recalls Additional Products, U.S. Food & Drug Administration (FDA)
• FDA approves first treatment for frequent urination at night due to overproduction of urine, U.S. Food & Drug Administration (FDA)
• Meijer Issues Allergy Alert On Mislabeled Pre-Made Caesar Salads Caesar Salads Mislabeled As Greek Salads Sold In Meijer Deli Sections, U.S. Food & Drug Administration (FDA)
• Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • Cosmetics News Update, U.S. Food & Drug Administration (FDA)
• Mutual Recognition promises new framework for pharmaceutical inspections for United States and European Union, U.S. Food & Drug Administration (FDA)
• Versa Marketing, Inc. Recalls Fusia Szechuan Stir Fry Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Cautions Pet Owners and Caretakers Not to Feed Certain Evanger’s or Against the Grain Canned Pet Foods, U.S. Food & Drug Administration (FDA)
• FDA approves Odactra for house dust mite allergies, U.S. Food & Drug Administration (FDA)
• New Blog: FDA’s Commitment to Women’s Heart Health Research, FDA Office of Women's Health
• Yoke's Fresh Market Issues Voluntary Cheese Recall, U.S. Food & Drug Administration (FDA)
• FDA approves Xermelo for carcinoid syndrome diarrhea, U.S. Food & Drug Administration (FDA)
• Lipari Foods Issues Voluntary Recall of Various Bulk and Retail Cheese Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• TECHNIVIE (fixed-dose combination of ombitasvir, paritaprevir, and ritonavir) label was updated to expand the indication, U.S. Food & Drug Administration (FDA)
• March EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Allergy Alert Issued in Two Massachusetts Whole Foods Market Stores for Undeclared Pecans in King Cakes, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Reopens Comment Period on Draft Guidance for Industry: Fruit Juice and Vegetable Juice as Color Additives in Food, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Edex (alprostadil for injection) 10 mcg 2 Pack by Endo Pharmaceuticals: Recall - Potential Lack of Sterility Assurance, FDA MedWatch
• Endo Pharmaceuticals Inc. Issues Voluntary Nationwide Recall for One Lot of Edex® (alprostadil for injection) 10 mcg 2 Pack Carton Due to Potential Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Whole Foods Market recalls “Our Chefs’ Own” Spinach Orzo Salad due to undeclared tree nut allergen, U.S. Food & Drug Administration (FDA)
• Manzana Products Co., Inc. Issues Voluntary Recall of Apple Sauces Due to Potential Presence of Foreign Material, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Avella Specialty Pharmacy Unexpired Sterile Injectable Products Labeled “Latex Free”: Recall - Products May Contain Synthetic or Natural Latex, FDA MedWatch
• Lakeview Cheese and Bashas’ Family of Stores Issue Voluntary Cheese Recall, U.S. Food & Drug Administration (FDA)
• Avella Specialty Pharmacy Issues Voluntary Nationwide Recall of all Sterile Products Produced at Advanced Pharma Houston Location from September 1, 2016 through February 16, 2017 Due to Potential Inaccuracy of Latex Free Label Reference, U.S. Food & Drug Administration (FDA)
• FDA clears test to help manage antibiotic treatment for lower respiratory tract infections and sepsis, U.S. Food & Drug Administration (FDA)
• FDA allows marketing of test to identify organisms that cause bloodstream infections and provide antibiotic sensitivity results, U.S. Food & Drug Administration (FDA)
• Kusher LLC Issues Allergy Alert on Undeclared Egg and Milk in Cookies, U.S. Food & Drug Administration (FDA)
• Raw milk isn't always healthier, FoodSafety.gov
• FDA MedWatch - XtraHRD Natural Male Enhancement Capsules by Organic Herbal Supply, Inc.: Recall - Undeclared Drug Ingredient, FDA MedWatch
• Louisiana drug and dietary supplement maker ordered to cease operations due to federal violations, U.S. Food & Drug Administration (FDA)
• Organic Herbal Supply, Inc. Announces a Voluntary Nationwide Recall of XtraHRD Natural Male Enhancement Capsules, U.S. Food & Drug Administration (FDA)
• Bee International issues Allergy Alert on Undeclared Milk in “Plastic Heart Tubes with Chocolate Lentils”, U.S. Food & Drug Administration (FDA)
• Biery Cheese Company Recalls Various Types Of Specialty Longhorn Colby Cheeses Due To Possible Listeria Monocytogenes Contamination, U.S. Food & Drug Administration (FDA)
• MDS Foods Inc, of Massillon, OH is Expanding the Current Recall to include Products Identified by Deutsch Kase Haus, LLC of Middlebury, Indiana from their 02/15/2017 Product Recall, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Approves Diroban, the First Generic Drug to Treat Heartworm Disease in Dogs, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Cautions Pet Owners and Caretakers Not to Feed Certain Evanger’s or Against the Grain Canned Pet Foods Due to Adulteration with Pentobarbital, U.S. Food & Drug Administration (FDA)
• Ditos Issues Allergy Alert on Undeclared Milk and Soy in Heart Plastic Platter Strawberries W/Dip with Chocolate Frosting and Heart Plastic Platter Mixed Fruit W/Dip with Chocolate Frosting, U.S. Food & Drug Administration (FDA)
• Saputo Inc. Recalls Certain Gouda Cheese Products Due to Potential Contamination of Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Veggie Noodle Co. Recalls Butternut Spirals Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Zimmer Biomet Recalls Comprehensive Reverse Shoulder due to a High Fracture Rate, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Comprehensive Reverse Shoulder by Zimmer Biomet: Class I Recall - High Fracture Rate, FDA MedWatch
• FDA approves new psoriasis drug, U.S. Food & Drug Administration (FDA)
• The FDA is issuing this recall notice from the Canadian Food Inspection Agency to alert U.S. consumers who may have purchased these products in Canada not to eat or serve them. The products under recall were manufactured specifically for the Canadian marketplace. - Updated Food Recall Warning - PC Organics brand baby food pouches recalled due to potential presence of dangerous bacteria, U.S. Food & Drug Administration (FDA)
• Allergen Alert Expansion: Legendary Baking Issues Allergy Alert - Almonds And Egg In Salted Caramel Chocolate Almond Pie - Allergens Not Declared In Ingredient List, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - CFSAN to Issue PDF Export Certificates for Food Products, U.S. Food & Drug Administration (FDA)
• Guggisberg Cheese, Inc. Recalls Various Colby Type Cheeses due to Possible Listeria Monocytogenes Contamination, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Announcing Public Meeting to Discuss Use of the Term “Healthy” in Food Labeling, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HCG (Human Chorionic Gonadotropin) Freeze Dried Vials by Synergy Rx: Recall - Lack of Sterility Assurance, FDA MedWatch
• Country Fresh Recalls Various Cooking And Snacking Products Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Against The Grain Pet Food Voluntarily Recalls One Lot of Pulled Beef Due to Potential Adulteration with Pentobarbital, U.S. Food & Drug Administration (FDA)
• Synergy Rx Pharmacy Issues Voluntary Nationwide Recall of All Lots of HCG (Human Chorionic Gonadotropin)Freeze Dried Vials Due to a Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Cousins Products LLC Issues Allergy Alert and Voluntary Recall on 16oz Creole Tomato Dressing, Best by Date 05/18/17, due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Against The Grain Pet Food Voluntarily Recalls One Lot of Pulled Beef Due to Potential Adulteration with Pentobarbital, U.S. Food & Drug Administration (FDA)
• Choice Farms LLC Recalls Very Limited Quantity of Mushrooms Stuffed with Cheese Supplied by a Third Party that may have the potential for Listeria monocytogenes Contamination, U.S. Food & Drug Administration (FDA)
• FDA approved class labeling revisions regarding the risk of hepatitis B virus reactivation in patients coinfected with hepatitis C virus (HCV) and hepatitis B virus (HBV), U.S. Food & Drug Administration (FDA)
• Sargento Recalls Select Products, U.S. Food & Drug Administration (FDA)
• MDS Foods Inc. - Food Safety Press Release, U.S. Food & Drug Administration (FDA)
• Meijer Recalls Meijer Brand Colby and Colby Jack Deli Cheeses Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• PetSmart Voluntarily Recalls Single Lot of Grreat Choice® Canned Dog Food Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - PetSmart Voluntarily Recalls Single Lot of Grreat Choice® Canned Dog Food Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Legendary Baking Issues Allergy Alert-Almonds and Egg in Salted Caramel Chocolate Almond Pie Allergens Declared but Listed Under “May Contain”, U.S. Food & Drug Administration (FDA)
• Exela Pharma Sciences, LLC Issues Voluntary Nationwide Recall of Ibuprofen Lysine Injection, 20 Mg/2 Ml (10 Mg/Ml) Due to Particulate Matter, U.S. Food & Drug Administration (FDA)
• Ruth’s Salad Charlotte NC Expands Recall of Ruth’s Salads Pimento Spreads due to Possible Health Risk. May Contain Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• FDA approves drug to treat Duchenne muscular dystrophy, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Cancer Drug for Dogs (Paccal Vet-CA1 ) No Longer Conditionally Approved, U.S. Food & Drug Administration (FDA)
• Federal judge approves consent decree with California dietary supplement distributor, Regeneca Worldwide, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Alaris Syringe Pump Module (Large Volume Pump), Model 8100 and AIL Sensor Kits by CareFusion: Class I Recall - Alarm Error, FDA MedWatch
• Medical Device Safety and Recalls: CareFusion Recalls Alaris Syringe Pump due to an Alarm Error Which May Cause Interruption of Therapy, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ibuprofen Lysine Injection, 20 mg/2 mL (10 mg/mL) by Exela Pharma Sciences: Recall - Particulate Matter, FDA MedWatch
• FDA MedWatch - Well Balance Xanthium & Siler Combo (Bi Yan Pian) Dietary Supplement by Kingsway Trading Inc.: Recall - Product Contains Banned Ephedra Alkaloids, FDA MedWatch
• Kingsway Trading Inc. Recalls “Xanthium & Siler Combo (Bi Yan Pian) Dietary Supplement” because it Contains Banned Ephedra Alkaloids, U.S. Food & Drug Administration (FDA)
• Fred Meyer Stores Issues Allergy Alert on Fred Meyer 100% Whole Wheat Bread due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Read about Research on Heart Disease in Women and more, FDA Office of Women's Health
• Starway Inc. Issues an Alert on Undeclared Sulfites in Peony Mark Brand Dried Lily Flower, U.S. Food & Drug Administration (FDA)
• Post-Game Plays: Food Safety Tips for Leftovers, FoodSafety.gov
• Update of CVM's What's New - Evanger’s Voluntarily Recalls Hunk of Beef Because Of Pentobarbital Exposure in one Batch of Food, U.S. Food & Drug Administration (FDA)
• The February 2017 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Evanger’s Voluntarily Recalls Hunk of Beef Because Of Pentobarbital Exposure in one Batch of Food, U.S. Food & Drug Administration (FDA)
• Today is National Wear Red Day, FDA Office of Women's Health
• Update of CVM's What's New - United States Files Enforcement Action Against Florida Company, U.S. Food & Drug Administration (FDA)
• Falafel King Issues Allergy Alert on Undeclared Milk in “Tzatziki Sauce”, U.S. Food & Drug Administration (FDA)
• Ruth’s Salad Charlotte NC is Recalling Ruth’s Original Pimento Spread 7 oz Because of Possible Health Risk. May Contain Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• February EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Sustiva (efavirenz) label was recently revised, U.S. Food & Drug Administration (FDA)
• Cosmetics News Update: How many cosmetic firms register with FDA? Latest report, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Chlorhexidine Gluconate: Drug Safety Communication - Rare But Serious Allergic Reactions, FDA MedWatch
• Update of CVM's What's New - Guidances Under Development for 2017, U.S. Food & Drug Administration (FDA)
• Le Fedou, Fromagerie De Hyelzas Sas Recalls “Tomme Brebis Fedou Cheese” and “Soureliette Cheese” because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Barberi International Inc. Recalls Frozen Ajiaco Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• New American Food Products, LLC Issues Allergy Alert on Weigels’s Mountain Valley and Royal Farms Market Place- Milk Chocolate Vanilla Caramels due to Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• U.S. Smokeless Tobacco Company Voluntarily Recalls Certain Smokeless Tobacco Products Manufactured at its Franklin Park, IL Facility, U.S. Food & Drug Administration (FDA)
• Your guide to a food-safe Super Bowl buffet, FoodSafety.gov
• Update of CVM's What's New - Animal Drug Approvals February 2017 Update, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Bard Peripheral Vascular Inc. Recalls Halo One Thin-Walled Guiding Sheath Due to Sheath Separation, Kinking, or Tip Damage, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - February 1, 2017, U.S. Food & Drug Administration (FDA)
• EVOTAZ (atazanavir/cobicistat) label was updated to include new data, U.S. Food & Drug Administration (FDA)
• Stribild (elvitegravir, cobicistat, emtrictiabine, tenofovir disoproxil fumarate) tablet label was revised to expand the patient population, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - How to Work with FDA on Food Guidance Documents, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Halo One Thin-Walled Guiding Sheath by Bard Peripheral Vascular Inc.: Class I Recall - Sheath Separation, Kinking, or Tip Damage, FDA MedWatch
• Medical Device Safety and Recalls: bioMerieux Recalls NucliSENS easyMAG Magnetic Silica and NucliSENS Magnetic Extraction Reagents due to Potential Inaccurate Test Results, U.S. Food & Drug Administration (FDA)
• NSE Products, Inc. Issues Allergy Alert on Undeclared Milk in Ageloc TR90 Protein Boost, U.S. Food & Drug Administration (FDA)
• Marich Confectionery Co. Issues Allergy Alert On Potential Undeclared Almonds In Product, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Certain Homeopathic Teething Products: FDA Warning - Confirmed Elevated Levels of Belladonna, FDA MedWatch
• FDA confirms elevated levels of belladonna in certain homeopathic teething products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - NucliSENS easyMAG Magnetic Silica and NucliSENS Magnetic Extraction Reagents by bioMerieux: Recall - Potential Inaccurate Test Results, FDA MedWatch
• Fred Meyer Recalls Bakery Fresh Goodness Carrot Cupcakes Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Carriage House Creations Recalls Carriage House Various Bourbon Basting Sauces and Hot Barbecue Sauce due to Undeclared Soy and Peanuts, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Toolbox and Guide for Consumer Food Safety Educators, U.S. Food & Drug Administration (FDA)
• Hospira Issues A Voluntary Nationwide Recall For One Lot Of Vancomycin Hydrochloride for Injection, USP Due To The Presence of Particulate Matter Within a Single Vial, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vancomycin Hydrochloride for Injection, USP by Hospira: Recall - Particulate Matter in Vial, FDA MedWatch
• CFSAN Constituent Update - Save the Date for a Public Meeting on the Use of the Term “Healthy”, 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)
• Athens Baking Company, Inc. Issues Voluntary Allergy Alert on Undeclared Milk in Harvest Whole Wheat Bread, U.S. Food & Drug Administration (FDA)
• Chip’n Dipped Voluntarily Expands Recall to Include 7 More of it’s Dark Chocolate Bars Due to Possible Presence of Undeclared Milk, U.S. Food & Drug Administration (FDA)
• King's Pastry Canada Issues Allergy Alert on Undeclared (Hazelnuts) In Various Cakes, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Announces Draft Guidance to Help Sprout Operations Comply with Produce Safety Rule, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - A Guide for Producers – Cattle Estrous Cycle and FDA-Approved Drugs to Control and Synchronize Estrus, U.S. Food & Drug Administration (FDA)
• D.F. Stauffer Biscuit Co., Inc. Issues Allergy Alert and Voluntary Recall on One Specific Best By Date Of 32oz Original Animal Crackers Due to Undeclared Milk Ingredient, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Blue Ridge Beef Recalls Product Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Statement from FDA Commissioner Robert Califf, M.D. announcing new draft guidances on medical product communications, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Warns of Illnesses and Deaths in Pets Exposed to Prescription topical (human) cancer treatment: Fluorouracil, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Requests Comments on Documents Related to Certain Biotechnology and Mosquito-related Products, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Requests Comments on Documents Related to Certain Biotechnology and Mosquito-related Products, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CFSAN Constituent Update - FDA Requests Comments on Documents Related to Certain Biotechnology and Mosquito-related Products, U.S. Food & Drug Administration (FDA)
• FDA and EPA issue final fish consumption advice, FDA Office of Women's Health
• CFSAN Constituent Update - Fish Consumption Advice, U.S. Food & Drug Administration (FDA)
• Blue Ridge Beef Recalls Product Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: UPDATE - Importance of Following Validated Reprocessing Instructions for PENTAX ED-3490TK Video Duodenoscopes: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - ED-3490TK Video Duodenoscope by Pentax: FDA Safety Communication - UPDATE - Follow Pentax Validated Reprocessing Instructions, FDA MedWatch
• Grange Co-Op Recalls Rogue All Purpose Rabbit Pellets For High Vitamin D Health Risk, U.S. Food & Drug Administration (FDA)
• Physio-Control Launches Voluntary Field Action for LIFEPAK 1000 Defibrillator, U.S. Food & Drug Administration (FDA)
• The Pictsweet Company Announces Voluntary Recall of Pictsweet Farms 12oz Breaded Okra due to Risk of Glass Contamination, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Grange Co-Op Recalls Rogue All Purpose Rabbit Pellets For High Vitamin D Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lifepak 1000 Defibrillators by Physio-Control: Voluntary Field Action - Immediately Remove and Reinstall Battery, FDA MedWatch
• Medical Device Safety and Recalls: FUJIFILM Medical Systems, U.S.A., Inc. removes certain older duodenoscope models from clinical use: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Golden Flake Snack Foods, Inc., Announces Voluntary Recall of Two Specific Product Code Lots of HOT Thin & Crispy 5.0 oz. Potato Chips Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Ban on Powdered Medical Gloves Applies to Veterinary Use, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals January 2017 Update (Green Book), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Duodenoscopes by Fujifilm Medical Systems: Safety Communication - Certain Older Models Removed From Clinical Use, FDA MedWatch
• CFSAN Constituent Update: FDA Issues Revised Draft Guidance for Control of Listeria monocytogenes in Ready-To-Eat Foods, U.S. Food & Drug Administration (FDA)
• Hy-Vee Voluntarily Recalls Several Candy Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Public Hearing on Partnerships to Enhance the Safety of Imported Foods, U.S. Food & Drug Administration (FDA)
• Tupperware U.S., Inc. Recalls Southwest Chipotle Seasoning Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Dutch Valley Food Distributors, Inc. Announces a Voluntary Nationwide Recall of Cappuccino Snack Mix For Potential Salmonella, U.S. Food & Drug Administration (FDA)
• New Look: January Women's Health Update, FDA Office of Women's Health
• Medical Device Safety and Recalls: Bayer Recalls Medrad Intego PET Infusion System Source Administration Sets due to Particulates Generated in Vial, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Provides Additional Time to Comment on Request For Information and Draft Guidance on Fiber on the Nutrition Facts Label, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - PNC-27 Products: FDA Warning – Do Not Use For Treatment or Cure for Cancer, FDA MedWatch
• FDA MedWatch - Medrad Intego PET Infusion System Source Administration Sets by Bayer: Recall - Particulates Generated in Vial, FDA MedWatch
• FDA MedWatch - Implantable Infusion Pumps in the Magnetic Resonance (MR) Environment: FDA Safety Communication - Important Safety Precautions, FDA MedWatch
• The J.M. Smucker Company Expands Limited Voluntary Recall on Certain Lots of Canned Cat Food Due to Low Levels of Thiamine (Vitamin B1), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - The J.M. Smucker Company Expands Limited Voluntary Recall on Certain Lots of Canned Cat Food, U.S. Food & Drug Administration (FDA)
• Chip’n Dipped Issues Allergy Alert on Undeclared Milk in "Dark Chocolate Crunch Bar", U.S. Food & Drug Administration (FDA)
• National Food Safety Education Conference: Registration Still Open!, FoodSafety.gov
• Mann Packing Voluntarily Issuing Class 1 Recall of Organic Veggies Snacking Tray, U.S. Food & Drug Administration (FDA)
• Palmer Candy Company Announces Voluntary Limited Recall of Select Candy Products, U.S. Food & Drug Administration (FDA)
• Hostess Brands, LLC Issues Voluntary Recall of Limited-Edition Holiday White Peppermint Hostess® Twinkies® because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Implantable Cardiac Devices and Merlin@home Transmitter by St. Jude Medical: FDA Safety Communication - Cybersecurity Vulnerabilities Identified, FDA MedWatch
• Medical Device Safety and Recalls: Cybersecurity Vulnerabilities Identified in St. Jude Medical's Implantable Cardiac Devices and Merlin@home Transmitter: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Harris Teeter, LLC Issues Voluntary Recall of Everroast Chicken Caesar Wrap for Undeclared Fish, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA To Provide Additional Time to Comment on Request For Information and Draft Guidance on Fiber on the Nutrition Facts Label, U.S. Food & Drug Administration (FDA)
• The January 2017 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Bakers of Paris Recalls Croissants Sold at Whole Foods Market® Stores in Northern California Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• Allergy Alert Issued in Select Whole Foods Market Stores for Undeclared Almond Flour in Tarts, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Nurse Assist Inc. Recalls Normal Saline Flush IV Syringes Due to Possible Burkholderia Cepacia Bloodstream Infections, U.S. Food & Drug Administration (FDA)
• The J.M. Smucker Company Announces a Limited Voluntary Recall on Certain Lots of Canned Cat Food Due to Low Levels of Thiamine (Vitamin B1), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Publishes Design Recommendations for Residue Studies in Honey, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Two Guidance Documents on the Nutrition Facts Label, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - The J.M. Smucker Company Announces a Limited Voluntary Recall on Certain Lots of Canned Cat Food, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: FDA Begins Posting Adverse Event Report Data for Foods and Cosmetics, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CFSAN Constituent Update: FDA Begins Posting Adverse Event Report Data for Foods and Cosmetics, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Announces Implementation of GFI #213, Outlines Continuing Efforts to Address Antimicrobial Resistance, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Conditionally Approves Tanovea-CA1, the first New Animal Drug for Treating Lymphoma in Dogs, U.S. Food & Drug Administration (FDA)
• January EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Mikesell’s Recalls 2.25 Oz. Nacho Cheese Tortilla Chips Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• How to safely prepare tamales and pasteles, FoodSafety.gov
• Route 11 Issues Voluntary Recall For Sour Cream & Chive Flavored Potato Chips, U.S. Food & Drug Administration (FDA)
• Texas Best Protein DBA Farm to Market Foods Issues Allergy Alert on Undeclared Peanut in Green Bean Casserole, U.S. Food & Drug Administration (FDA)
• TreeHouse Foods Amends Best By Dates in Voluntary Product Recall of Macaroni & Cheese Cup Products, U.S. Food & Drug Administration (FDA)
• American Roland Food Corp. Initiates A Recall Of Roland® Manzanilla Olives Stuffed With Anchovies Due To Product Quality Issue, U.S. Food & Drug Administration (FDA)
• Whitestone Feeds, Inc. Announces Voluntary Recall of all JES Premium 40 Tubs due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Comment Period Extension for “Healthy” Claim for Food Labeling, U.S. Food & Drug Administration (FDA)
• Huvepharma, Inc. Issues Voluntary Nationwide Recall of Duramycin-10 Due to Stability Failure, U.S. Food & Drug Administration (FDA)
• How to safely cook and serve meat dishes, FoodSafety.gov
• Herr Foods Inc. Announces Voluntary Recall of Herr’s Brand of Smoked Chipotle Flavored Kettle Cooked Potato Chips and Peddler’s Pantry Smoked Dried Chipotle Kettle Cooked Potato Chips due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Southeastern Mills, Inc. Announces Recall of Certain Food Ingredients and Food Mixes Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves first drug for spinal muscular atrophy, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: FDA Warns Health Care Providers Against Relying Solely on Zika Virus Serological IgM Assay Results; Reminds them to Wait for Confirmatory Test Results Before Making Patient Management Decisions: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - ZIKV Detect IgM Capture ELISA by InBios International, Inc: FDA Safety Communication - Wait for Confirmatory Test Results Before Making Patient Management Decisions, FDA MedWatch
• Update of CVM's What's New - Update on Implementation of FDA’s Guidance for Industry #213, U.S. Food & Drug Administration (FDA)
• Holiday food safety for pregnant women, FoodSafety.gov
• Fresh Express Announces Precautionary Recall of a Limited Quantity of 9 oz. Hearts of Romaine Salad Due to Possible Allergen Exposure, U.S. Food & Drug Administration (FDA)
• Bickel's Snack Foods Notice of Voluntary Recall, U.S. Food & Drug Administration (FDA)
• Herrs Announces Voluntary Recall of Chipotle-Flavored Chips, U.S. Food & Drug Administration (FDA)
• Dawn Food Products Recalls Limited Quantities of Bulk Bakery Mix Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• House-Autry Mills Announces Voluntary Recall of Limited Products Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• 4 Holiday Food Safety Tips, FDA Office of Women's Health
• Update of CVM's What's New - FDA Annual Summary Report on Antimicrobials Sold or Distributed in 2015 for Use in Food-Producing Animals, U.S. Food & Drug Administration (FDA)
• H-E-B Expands Recall On Raw Shelled Pistachios, U.S. Food & Drug Administration (FDA)
• Dieffenbach's Potato Chips Inc. Issues Voluntary Recall for Sour Cream & Onion Kettle Chips Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Rich Products Corporation Issues Nationwide Allergy Alert on Undeclared Walnuts in Certain Ice Cream Cake Products, U.S. Food & Drug Administration (FDA)
• 4 steps for safely roasting a pig, FoodSafety.gov
• CFSAN Constituent Update - FDA Issues Draft Guidance Recommending a Limit on the Amount of Lead in Lipstick and Other Cosmetics, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA’s Strategy for FSMA Training: An Update, U.S. Food & Drug Administration (FDA)
• Altijira Murray Products, LLC Recalls Selected Ice Cream Products Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Standard Offset Cup Impactor with POM-C Handle by Greatbatch Medical: Class I Recall - Inadequate Sterilization, FDA MedWatch
• Medical Device Safety and Recalls: Greatbatch Medical Recalls Standard Offset Cup Impactor Used for Hip Joint Replacement due to Inadequate Sterilization, U.S. Food & Drug Administration (FDA)
• VanLaw Food Products, Inc. Announces Voluntary Recall of WinCo Brand Ranch Dressing, U.S. Food & Drug Administration (FDA)
• H-E-B Issues Voluntary Recall On Bakery Products, U.S. Food & Drug Administration (FDA)
• Food Recall Warning - Snyder of Berlin Buffalo Blue Kettle Cooked Potato Chips Recalled Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• December Women's Health Update, FDA Office of Women's Health
• Holiday treat or unsafe to eat?, FoodSafety.gov
• FDA grants accelerated approval to new treatment for advanced ovarian cancer, U.S. Food & Drug Administration (FDA)
• Houdini Inc. Recalls Blue Cheese Savory Twists, 7 Oz Box Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Poppies International, Inc. Battleboro, North Carolina Recalls Mini Eclairs and Chocolate Covered Cream Puffs Because of Potential Health Risks, U.S. Food & Drug Administration (FDA)
• Williams-Sonoma Announces the Voluntary Recall of Meyer Lemon Poppy Quick Bread, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Chantix (varenicline) and Zyban (bupropion): Drug Safety Communication - Mental Health Side Effects Revised, FDA MedWatch
• 3 most common food prep questions, FoodSafety.gov
• FDA Bans Powdered Surgeon Gloves; Powdered patient examination gloves; Absorbable Powder for Surgeon’s Glove, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: FDA Issues Interim Final Rule Allowing More Raw Fruits and Vegetables to Bear Health Claims about Relationship between Dietary Saturated Fat and Cholesterol and the Risk of Coronary Heart Disease, U.S. Food & Drug Administration (FDA)
• Ron’s Home Style Foods, Inc. Recalls Tropical Fruit Supreme, Pineapple Nut Delight, and Pistachio Crème Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Arcadia Trading Inc. Recalls Lizard Fish Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New CVM Center Director Announced, U.S. Food & Drug Administration (FDA)
• Old Dutch Recalls Various Flavored Potato Chip Products due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Ridley Block Operations Announces Voluntary Recall of Ultralyx 24% + 3% Mag Composite, U.S. Food & Drug Administration (FDA)
• New Hope Mills Expands Recall of Limited Amounts of Crepe Mix as a Precaution Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Recall of beef cattle feed product, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Extension of Comment Period, U.S. Food & Drug Administration (FDA)
• H-E-B Issues Recall On Raw Shelled Pistachios, U.S. Food & Drug Administration (FDA)
• Thomas Hammer Coffee Roasters Inc. Issues Allergy Alert on Undeclared Milk, Egg, Soy, Wheat in The Cranberry Orange Scone, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Issues Guidance Recommending Global Standards for Bioequivalence Study, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Concludes Consultation on Pink Flesh Pineapple, U.S. Food & Drug Administration (FDA)
• FDA approves Eucrisa for eczema, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - General Anesthetic and Sedation Drugs: Drug Safety Communication - New Warnings for Young Children and Pregnant Women, FDA MedWatch
• Linden Cookies Issues Allergy Alert on Undeclared Milk in Mini Chocolate Chip Cookies and 3 Pack Chocolate Chip Cookies, U.S. Food & Drug Administration (FDA)
• FDA approves first autologous cellularized scaffold for the repair of cartilage defects of the knee, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Finalizes FSMA Third-Party Certification User Fee Program, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Clarifies Applicability of Color Additive Regulations for Vegetable and Fruit Juice, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Centurion Recalls Multi-Med Single Lumen Catheters due to Excess Material that May Split or Separate, U.S. Food & Drug Administration (FDA)
• Brand Castle, LLC Recalls Limited Quantities of 16oz. Boxes of In The Mix® Monkey Bread Mix Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Lenny & Larry’s, Inc. Conducts Nationwide Voluntary Recall of Chocolate Chip and Coconut Chocolate Chip Complete Cookie Recall Due To Possible Undeclared Milk in Dark Chocolate Chips, U.S. Food & Drug Administration (FDA)
• Fourth Street Barbecue, Inc. /Packing Division Recalls Mac & Cheese Dinner Cups Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• New Hope Mills Recalls Limited Amounts of Crepe Mix as a Precaution Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• TreeHouse Foods Announces Voluntary Product Recall Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Valley Milk Products, Strasburg, Virginia Recalls Limited Amount of Milk and Buttermilk Powder Because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• Shearer's Foods, LLC Recalls Product Made With Affected Seasonings Due To Potential Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Pioglitazone-containing Medicines: Drug Safety Communication - Updated FDA Review, Increased Risk of Bladder Cancer, FDA MedWatch
• FDA Cosmetics News: Using Adverse Event Reports to Monitor Cosmetic Safety, U.S. Food & Drug Administration (FDA)
• Blue Ridge Beef of Eatonton, GA Recalls Product Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Advises Consumers Not to Eat Apple Tree Goat Dairy Goat Cheese Products Because of Possible Listeria Contamination, U.S. Food & Drug Administration (FDA)
• Boulder Brands, Inc. Voluntarily Recalls Earth Balance Vegan White Cheddar Mac & Cheese and Earth Balance Vegan Cheddar Mac & Cheese Due to Possible Dairy Allergen Contamination, U.S. Food & Drug Administration (FDA)
• Deep River Snacks Issues Voluntary Recall For Sour Cream & Onion Kettle Chips Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Convenience Kits Containing Multi-Med Single Lumen Catheters by Centurion: Class I Recall - Excess Material May Split or Separate, FDA MedWatch
• Update of CVM's What's New - Blue Ridge Beef of Eatonton, GA Recalls Product Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA takes action against four tobacco manufacturers for illegal sales of flavored cigarettes labeled as little cigars or cigars, U.S. Food & Drug Administration (FDA)
• FDA Cosmetics News: How many cosmetic firms register with FDA? Latest report, U.S. Food & Drug Administration (FDA)
• 'Tis the season for holiday food safety tips, FoodSafety.gov
• Update of CVM's What's New - Animal Drug Approvals December 2016 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Stonewall Kitchen Recalls Limited Quantities of Cinnamon Apple, Orange Cranberry and Toasted Coconut Pancake & Waffle Mixes as a Precautionary Measure Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FAIRWAY “LIKE NO OTHER MARKET” Recalls FAIRWAY Brand Candy Corn Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Publix Recalls Publix Premium Pancake and Waffle Mixes Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Publix Recalls Publix Premium Pancake and Waffle Mixes Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Application Reminder: Firms Intending to Ship Dairy Products to Chile, China, or the European Union, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Using Adverse Event Reports to Monitor Cosmetic Safety, U.S. Food & Drug Administration (FDA)
• Oriental Packing Co., Inc. Issues Another Recall Alert on Lead in Curry Powder, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Draft Guidance on Food Contact Substances for Use with Infant Formula and Human Milk, U.S. Food & Drug Administration (FDA)
• The December 2016 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Voluntary Class II Recall of Chocolate Hazelnut Butter CLIF® Nut Butter Filled, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Guidance for Industry about Model Accreditation Standards for Third-Party Certification Bodies, U.S. Food & Drug Administration (FDA)
• FMIF Holdings, LLC Urges Consumers of 8oz Pods Purchased Online to Dispose of Product Immediately, U.S. Food & Drug Administration (FDA)
• Keep food safety guidance at hand..., FoodSafety.gov
• Phil-Am Trading, Inc. Recalls Phil-Am Smoked Mackerel (Hasa-Hasa) Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Royal Seafood Baza, Inc. Recalls Various Ready to Eat Herring Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Consumer Advisory, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA to Align Menu Labeling Compliance Date with the Enforcement Date for Menu Labeling to May 5, 2017, U.S. Food & Drug Administration (FDA)
• FDA approves Jardiance to reduce cardiovascular death in adults with type 2 diabetes, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Revises CPG on Extralabel Use of Medicated Feeds for Minor Species, U.S. Food & Drug Administration (FDA)
• Derby City Vending Issues Allergy Alert of Undeclared Milk, Egg And Soy in their Buffalo Chicken Sandwich, U.S. Food & Drug Administration (FDA)
• Food safety tips for World HIV/AIDS Day, FoodSafety.gov
• Update of CVM's What's New - Intermountain Farmers Association Issues Recall of Rabbit Feed for High Vitamin D Content, U.S. Food & Drug Administration (FDA)
• Bakkavor Foods USA, Inc. Issues Voluntary Recalls of Certain Hummus Products Because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Bakkavor Foods USA, Inc. Issues Voluntary Recalls of Certain Hummus Products Because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• Intermountain Farmers Association Issues Recall of Rabbit Feed for High Vitamin D Content, U.S. Food & Drug Administration (FDA)
• Ultimate Body-Tox Issues a Nationwide Voluntary Recall of Ultimate Body Tox PRO Found to Contain Undeclared Sibutramine, U.S. Food & Drug Administration (FDA)
• MS Bionic, Inc. Issues a Voluntary Nationwide Recall of All Lots of Megajex Natural Male Sex Enhancer Dietary Supplement, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Medtronic Recalls Neurovascular Products due to Potential Separation and Detachment of Polytetrafluoroethylene (PTFE) Coating, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Megajex Natural Male Sex Enhancer by MS Bionic: Recall - Undeclared Drug Ingredients, FDA MedWatch
• FDA MedWatch - Ultimate Body Tox PRO: Recall - Undeclared Drug Ingredient, FDA MedWatch
• Food regulators seize adulterated milk products for food safety violations, U.S. Food & Drug Administration (FDA)
• Product Label Missing Milk and Fish Allergen Advisory in Blue Crab Mini Crab Cakes, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Secondhand (and Third-hand) Smoke May Be Making Your Pet Sick, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Announces Minor Use/Minor Species (MUMS) Grant Application Open Period Due January 13, 2017, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Clarification on Menu Labeling Compliance Date, U.S. Food & Drug Administration (FDA)
• Caregiving and Diabetes: Lending a Helping Hand, FDA Office of Women's Health
• Calbee North America Issues Allergy Alert On Undeclared Milk In Harvest Snap Black Pepper Snap Pea Crisps, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Calbee North America Issues Allergy Alert On Undeclared Milk In Harvest Snap Black Pepper Snap Pea Crisps, U.S. Food & Drug Administration (FDA)
• December EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Anderson’s Frozen Custard issues Allergy Alert on Undeclared Peanuts in Pumpkin Ice Cream Pies, U.S. Food & Drug Administration (FDA)
• JFC International Inc. Issues Allergy Alert On Undeclared Wheat In You-Ka Fresh Ramune And You-Ka Punch Ramune, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Products Containing Belladonna Extract by Raritan Pharmaceuticals: Recall - Possible Belladonna Alkaloids, FDA MedWatch
• Recall Announcement: Sabra Dipping Company’s Recall of Hummus Prompts Secondary Recall of Mediterranean Chicken Hummus Sandwich, U.S. Food & Drug Administration (FDA)
• Raritan Pharmaceuticals Inc. Issues a Voluntary Nationwide Recall of Products Containing Belladonna Extract Due to the Possibility of the Presence of Belladonna Alkaloids, U.S. Food & Drug Administration (FDA)
• National Recall by Sabra Dipping Company Leads to Secondary Recall of Deli Sandwich in Pittsburg (PA), Cleveland (OH) and Buffalo (NY) Markets, U.S. Food & Drug Administration (FDA)
• Nutrivitashop, A DBA of Naturecom Inc is Requesting the Voluntarily Recall of DMAA Net Weight 500g Due to the Presence of DMAA that may Pose Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Handy Seafood Recall: Product Label Missing Milk and Fish Allergen Advisory in Whole Foods Blue Crab Mini Crab Cakes, U.S. Food & Drug Administration (FDA)
• Sabra Dipping Company’s Recall Prompts Secondary Recall of Mediterranean Style Chicken With Hummus Sandwiches in Washington Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• National Recall by Sabra Dipping Company Leads to Secondary Recall of Deli Sandwich in Northern California and Nevada, U.S. Food & Drug Administration (FDA)
• Plan ahead to make the most of your leftovers, FoodSafety.gov
• Sabra Dipping Company’s Recall Prompts Secondary Recall of Vegetable Products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - FindrWIRZ Guidewire System by SentreHeart: Class I Recall - Coating Separation, FDA MedWatch
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update: Warning & Untitled Letters to Industry Citing Color Additive Violations, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: SentreHeart Recalls FindrWIRZ Guidewire System due to Coating Separation, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Request For Information and Draft Guidance on Fiber, U.S. Food & Drug Administration (FDA)
• 6 ways to cook a turkey, FoodSafety.gov
• Cantrell Drug Company Issues Voluntary Recall of Select Sterile Drug Products Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tri-Coast Pharmacy Sterile Products: Recall - Lack of Sterility Assurance, FDA MedWatch
• Tri-Coast Pharmacy Inc. Voluntarily Recalling All Sterile Products Prepared Between May 17, 2016 and November 17, 2016 Due to Concern Over Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sterile Drug Products by Cantrell Drug Company: Recall - Lack of Sterility Assurance, FDA MedWatch
  • <Possible follow-ups>
  • FDA MedWatch - Sterile Drug Products by Cantrell Drug Company: Recall - Lack of Sterility Assurance, FDA MedWatch
• Allergy Alert Issued on Mislabeled Product for Undeclared Milk and Soy in Heinz Homestyle Bistro Au Jus Gravy, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Removes Approval for the Use of PFCs in Food Packaging Based on the Abandonment, U.S. Food & Drug Administration (FDA)
• Sabra Dipping Company Issues Voluntary Recall Of Certain Hummus Products Because Of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• H-E-B Issues Precautionary Baby Food Recall, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Advises Consumers of Recall of Certain Sabra Hummus Products, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Releases 2014 NARMS Integrated Report; Finds Measurable Improvements in Antimicrobial Resistance Levels, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GNC Women’s Ultra Mega Time Release 180 count Dietary Supplement by Nutra Manufacturing: Recall - Undeclared Milk, FDA MedWatch
• Nutra Manufacturing, Inc. Announces Nationwide Voluntary Recall of One Lot of GNC Women’s Ultra Mega Time Release 180 count Dietary Supplement, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - 2017 Consumer Food Safety Education Conference Early Bird Registration Rate Closes December 1, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Video Available - Veterinary Feed Directive - an Overview, U.S. Food & Drug Administration (FDA)
• Request Foods, Inc. Issues Allergy Alert On Undeclared Eggs In GFS® Brand Cheese Manicotti, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Finalizes Report on the Regulation of Combination Drug Medicated Feeds, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Reopens Comment Period on Draft Guidance Concerning Structure/Function Claims, U.S. Food & Drug Administration (FDA)
• FDA research to help speed development of Zika virus vaccines and therapeutics, U.S. Food & Drug Administration (FDA)
• Read about Essure, Caregiving and more, FDA Office of Women's Health
• CFSAN Constituent Update - Food Safety Survey, U.S. Food & Drug Administration (FDA)
• Do you know the 3 ways to safely thaw a turkey?, FoodSafety.gov
• CFSAN Constituent Update - FDA Shares Data from Ongoing Sampling Program, U.S. Food & Drug Administration (FDA)
• FDA approves Intrarosa for postmenopausal women experiencing pain during sex, U.S. Food & Drug Administration (FDA)
• The Popcorn Shoppe Issues Allergy Alert on Undeclared Milk and Soy in Olde Tyme Recipe Popcorn Balls, Edwards Orchard Popcorn Balls and Edwards Orchards West Popcorn Balls, U.S. Food & Drug Administration (FDA)
• Marine Agrifuture, LLC. Recalls "Kahuku Ogo", “Robusta Ogo” and “Kahuku Sea Asparagus” Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• 4C Foods Corp. Voluntarily Recalls 4C Grated Cheese, Homestyle Grated Cheese, and Cento Grated Cheese Brands NET WT. 6 OZ Glass Jars Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Essure labeling with important safety information for patients and physicians, FDA Office of Women's Health
• FDA MedWatch - Essure Permanent Birth Control System by Bayer Healthcare: FDA Announcement - Label Changes, FDA MedWatch
• To Wash or Not Wash?, FoodSafety.gov
• Voluntary Recall of Weight Watchers Smart Ones Chocolate Chip Cookie Dough Sundae Due to Possible Health Risks from Cookie Dough Pieces Purchased from a Third Party Supplier, U.S. Food & Drug Administration (FDA)
• Cedar Crest Specialties, Inc. Issues Recall on Chocolate Chip Cookie Dough, Monster Cookie and Pirate's Bounty Ice Cream as a Result of Aspen Hills, Inc. Cookie Dough Recall, U.S. Food & Drug Administration (FDA)
• Ashby's Sterling Ice Cream Recalls Peanut Butter Landslide Ice Cream Due to Health Risk; This is Related to Expanded Recall by Outside Supplier Aspen Hills, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Approves Itrafungol, a New Animal Drug for Treating Ringworm in Cats, U.S. Food & Drug Administration (FDA)
• Free2b Foods Issues Allergy Alert on Undeclared Milk Ingredient in Chocolate Sun Cups, U.S. Food & Drug Administration (FDA)
• Chocolate Shoppe Ice Cream Company EXPANDS Recall Of Select Products Containing Chocolate Chip Cookie Dough Pieces Purchased From Outside Supplier Aspen Hills Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Agave Dream Recalls Several Flavors Of Ice Creams In Pint Size Containers Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approved VEMLIDY to treat hepatitis B virus, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Releases Final Guidance for Voluntary Qualified Importer Program, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA's Voluntary Qualified Importer Program: Guidance for Industry, U.S. Food & Drug Administration (FDA)
• 6 Resources for American Diabetes Month, FDA Office of Women's Health
• ISB Food Group, LLC Recalls L.A. Creamery Honeycomb Ice Cream And L.A. Creamery Salted Caramel Ice Cream With Expiration Dates Of March 18, 2017 Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• ISB Food Group, LLC Recalls Nancy’s Fancy Butterscotch Budino Gelato And Nancy’s Fancy Peanut Butter With Crunchy Peanuts Gelato With Expiration Dates Of March 18, 2017 Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Food safety myths vs. facts: Thanksgiving cooking edition, FoodSafety.gov
• FDA MedWatch - Skinny Bee Diet by Love My Tru Body: Recall - Undeclared Drug Ingredients, FDA MedWatch
• Love My Tru Body Issues Voluntary Nationwide Recall of Skinny Bee Diet Due To Presence of Undeclared Sibutramine, Desmethylsibutramine and/Phenolphthalein, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Side Head Regulator TT Tablet by Life Rising/Ton Shen Health: Recall - Elevated Levels of Lead, FDA MedWatch
• Ton Shen Health Recalls Life Rising Brand “Side Head Regulator TT Tablet” Because of Possible Health Risk for Children Under the Age of 18, U.S. Food & Drug Administration (FDA)
• SHRI SHIVA Foods Inc. Recalls "MTR Sambar Powder" Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Selzentry approved for pediatric use, U.S. Food & Drug Administration (FDA)
• Crescent Vending Co. Issues Allergy Alert on Undeclared (Wheat, Soy, Milk, And Egg) in Product, U.S. Food & Drug Administration (FDA)
• OLMA-XXI, Inc. Recalls Two Smoked Fish Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Flu.Gov is now redirecting to CDC/flu, Centers for Disease Control and Prevention (CDC)
• McConnell’s Fine Ice Creams Recalls Select 16oz. Packages Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Select Whole Foods Market Stores in Mid-Atlantic Region Issues Allergy Alert Due to Undeclared Eggs, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals November 2016 Update, U.S. Food & Drug Administration (FDA)
• The November 2016 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• ICAPP Voluntarily Recalls Certain Lots of Frozen Strawberries, U.S. Food & Drug Administration (FDA)
• Thanksgiving planning made easy, FoodSafety.gov
• AC Creamery Inc. Recalls "Manila Sky Purple Yumm Ice Cream" Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• November EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• FDA Veterinarian - November 1, 2016, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Releases Revised Guidance about Animal Drug User Fees, Fee Waivers and Reductions, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - FDA Releases Revised Guidance about Animal Drug User Fees, Fee Waivers and Reductions, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: HeartWare Recalls Ventricular Assist Device Controllers Due to Loose Connectors which may Prevent Alarm from Sounding and Pump Stops, U.S. Food & Drug Administration (FDA)
• Mondelēz Global LLC Conducts Nationwide Voluntary - Recall of Oreo Fudge Cremes Product Sold in the U.S. Recall Due to Milk Allergen Not Listed in Ingredient Line, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HeartWare Ventricular Assist Device (HVAD) Pumps by HeartWare Inc.: Class I Recall - Loose Connectors May Prevent Alarm from Sounding, FDA MedWatch
• FDA approves new device for prevention of recurrent strokes in certain patients, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New FSMA Guidance, U.S. Food & Drug Administration (FDA)
• New Guidance: Labeling for Permanent Hysteroscopically-Placed Tubal Implants Intended for Sterilization, FDA Office of Women's Health
• Back to Nature Issues a Product Recall and Allergy Alert for Chocolate Chunk Cookies, Mini Chocolate Chunk Cookies and Chocolate Granola Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Seeks Public Comments on Updating Tolerances for Residues of New Animal Drugs in Food, U.S. Food & Drug Administration (FDA)
• Stewart's Shops Issues Allergy Alert On Undeclared Milk In Sportade Fruit Punch, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - TAH-t Companion 2 Driver System (C2) and Freedom Driver System by SynCardia Systems: Letter to Health Care Providers - Mortality and Neurological Adverse Event Results, FDA MedWatch
• FDA MedWatch - Testosterone and Other Anabolic Androgenic Steroids (AAS): FDA Statement - Risks Associated With Abuse and Dependence, FDA MedWatch
• Trick or treat, safe to eat?, FoodSafety.gov
• Update of CVM's What's New - Search Approved Animal Drugs on the Redesigned Animal Drugs @ FDA, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - SCORE Hits the Ground Running, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: St. Jude Medical Recalls Implantable Cardioverter Defibrillators (ICD) and Cardiac Resynchronization Therapy Defibrillators (CRT-D) Due to Premature Battery Depletion, U.S. Food & Drug Administration (FDA)
• Draft Guidance on Developing Drugs for Treatment of Low Sexual Desire, Interest or Arousal, FDA Office of Women's Health
• Medical Device Safety and Recalls: HeartWare Recalls Ventricular Assist Device Pumps Due to Contamination Causing Electrical Issues, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HeartWare Ventricular Assist Device (HVAD) Pumps by HeartWare Inc. : Class I Recall - Contamination Causing Electrical Issues, FDA MedWatch
• Brownwood Farms Issues Allergy Alert On Undeclared Milk In Fruit Preserves And Fruit Butter Products, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: TeleFlex Medical Recalls Tracheostomy Tube Set Due to Possible Disconnection During Patient Use, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Willy Rusch Tracheostomy Tube Set by TeleFlex Medical: Class I Recall - Possible Disconnection During Patient Use, FDA MedWatch
• FDA MedWatch - Radiation Therapy Devices by Multidata Systems International: Discontinue Use – Concerns about Risks to Patients, FDA MedWatch
• Mammography Awareness for All Women, FDA Office of Women's Health
• October is National Cybersecurity Awareness Month: The Importance of Cybersecurity and Medical Devices, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Veterinary Regenerative Medicine & Animal Cell-Based Products, U.S. Food & Drug Administration (FDA)
• Yoma Myanmar Tea Co. Issues Allergy Alert on Undeclared Peanuts in Yoma Myanmar Tea Salad Snack, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medtronic Neurovascular Products: Recall - Potential Separation and Detachment of Polytetrafluoroethylene (PTFE) Coating, FDA MedWatch
• Medtronic Announces Voluntary Recall of its Pipeline Embolization Device, Alligator Retrieval Device, X-Celerator Hydrophilic Guidewire, Ultraflow and Marathon Flow Directed Micro Catheters, U.S. Food & Drug Administration (FDA)
• Voluntary Recall Notice of McCormick 24 oz. Club Size Original Taco Seasoning Mix Due to Unlabeled Milk Allergen, U.S. Food & Drug Administration (FDA)
• FDA awards 21 grants to stimulate product development for rare diseases, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Leonhard Lang Multi-function Defibrillation Electrodes DF29N Will Not Work with Welch Allyn Automatic External Defibrillator model AED 10, U.S. Food & Drug Administration (FDA)
• Kuster's, Inc. Voluntarily Recalls Product Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Turkey Hill Dairy Issues Class I Voluntary Recall of Select Dutch Chocolate Premium Ice Cream - 48 oz. size, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Skintact DF29N Multi-function Defibrillation Electrodes by Leonhard Lang: Class I Recall - Connector Compatibility Issue, FDA MedWatch
• Get ready for Global Handwashing Day, FoodSafety.gov
• Medical Device Safety and Recalls: Updated Safety Communication on Mycobacterium chimaera Infections associated with LivaNova PLC Stӧckert 3T Heater-Cooler System, U.S. Food & Drug Administration (FDA)
• Brownwood Farms Issues Allergy Alert and Recall of Products Based on Possible Health Risk Associated With Undeclared Soy or Yellow #5 Food Coloring, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Stӧckert 3T Heater-Cooler System by LivaNova PLC (formerly Sorin Group Deutschland GmbH): UPDATED Safety Communication - Reports of Mycobacterium Chimaera Infections, FDA MedWatch
• CFSAN Constituent Update - What to Expect Now that the First Big FSMA Compliance Dates Are Here, U.S. Food & Drug Administration (FDA)
• Read about Breast Cancer, Clinical Trials and more, FDA Office of Women's Health
• Nutrisystem Retail Division Voluntarily Recalls One Product Containing Chocolate Cookie Dough Pieces Purchased From Third Party Supplier Due To A Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Roland Foods, LLC, Initiates A Voluntary Recall of Roland® Preserved Lemons Due to Undeclared Sulfites in Product, U.S. Food & Drug Administration (FDA)
• Publix Recalls Publix Premium Chocolate Chip Cookie Dough Ice Cream Due To Possible Listeria monocytogenes Contamination From Aspen Hills, Inc. Cookie Dough Pieces, U.S. Food & Drug Administration (FDA)
• Chocolate Shoppe Ice Cream Company Recalls Select Products Containing Chocolate Chip Cookie Dough Pieces Purchased From Outside Supplier Aspen Hills Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Blue Bunny Hoppin’ Hollidoodle Ice Cream Voluntary Recall, U.S. Food & Drug Administration (FDA)
• Outside Supplier Aspen Hills Expands Cookie Dough Recall; Blue Bell Recalls All Products Made With Aspen Hills Cookie Dough Due To Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Mars Petcare US Announces Voluntary Recall of Limited Number of CESAR® Classics Filet Mignon Flavor Wet Dog Food Because of Potential Presence of Plastic, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Mars Petcare US Announces Voluntary Recall of Limited Number of CESAR® Classics Filet Mignon Flavor Wet Dog Food Because of Potential Presence of Plastic, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) by St. Jude Medical: FDA Safety Communication - Batteries May Fail Earlier Than Expected, FDA MedWatch
• Medical Device Safety and Recalls: Premature Battery Depletion of St. Jude Medical ICD and CRT-D Devices: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Nestlé USA Initiates Voluntary Recall Of Nestlé® Drumstick® Club 16 Count Variety and 24 Count Vanilla Pack Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Osage Gardens Inc. Recalls Osage Gardens Organic 2oz Micro Greens Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Le Petit Belge, LLC Issues Allergy Alert on Undeclared Milk in Belgian Boys Mini Pancakes, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Baxter Corporation Recalls 50 mm 0.2 Micron Filter Due to the Potential for a Missing Filter Membrane and Possible Particulate Matter Contamination, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Compliance Dates for Nutrition Initiatives, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - October 2016 Animal Drug Approvals, U.S. Food & Drug Administration (FDA)
• Enforcement Report Upgrades, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Manufactured Food Regulatory Program Standards 2016 Updates, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Twin-Pass Dual Access Catheters by Vascular Solutions: Recall - Potential for Excess Manufacturing Material At The Tip, FDA MedWatch
• FDA MedWatch - I.V. Flush Syringes by Nurse Assist: Recall - Potential Link to Burkholderia Cepacia Bloodstream Infections, FDA MedWatch
• Food Safety for Fall Outings, FoodSafety.gov
• CFSAN Constituent Update - National Food Safety Education Conference 2017 – Registration Now Open, U.S. Food & Drug Administration (FDA)
• Vascular Solutions, Inc. Issues Recall of Twin-Pass® Dual Access Catheters, U.S. Food & Drug Administration (FDA)
• Nurse Assist Initiates Nationwide Voluntary Recall of All Unexpired Lots of I.V. Flush Syringes, U.S. Food & Drug Administration (FDA)
• FDA warns about the risk of hepatitis B reactivating in some patients treated with direct-acting antivirals for hepatitis C, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Direct-Acting Antivirals for Hepatitis C: Drug Safety Communication - Risk of Hepatitis B Reactivating, FDA MedWatch
• Good Earth Egg Company Voluntarily Recalls Shell Eggs Because of a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 50mm 0.2 Micron Filters by Baxter: Recall - Potential for Missing Filter Support Membrane, Particulate Matter, FDA MedWatch
• Baxter Initiates Voluntary Recall of All Unexpired Lots of 50mm 0.2 Micron Filters, U.S. Food & Drug Administration (FDA)
• Spices USA Inc. Issues Alert on Elevated Levels of Lead in Ground Turmeric, U.S. Food & Drug Administration (FDA)
• Fred Meyer Recalls Deli Superfood Wrap Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Fresh Express Announces Precautionary Recall of a Limited Quantity of 11 oz. American Salad due to Possible Allergen Exposure, U.S. Food & Drug Administration (FDA)
• Graceleigh, Inc. Recalls Sammy’s Milk Baby Food Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• October EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• FDA MedWatch - Homeopathic Teething Tablets and Gels: FDA Warning - Risk to Infants and Children, FDA MedWatch
• FDA warns against the use of homeopathic teething tablets and gels, U.S. Food & Drug Administration (FDA)
• The October 2016 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• McCain Foods USA, Inc. Announces a Product Recall Impacting Frozen Onion Rings Sold and Distributed Under Four Separate Private Label Retail Brands, U.S. Food & Drug Administration (FDA)
• Updated Recall Information: McCain Foods USA, Inc. Issues Expanded Allergy Alert on Undeclared Milk in Frozen Onion Rings Sold and Distributed Under Private Label Retailer Brands, U.S. Food & Drug Administration (FDA)
• Comment Request Regarding Proposed Agency Information Collection Activities Regarding Risk Factor Elicitation for the Transfusion-Transmissible Infection Monitoring System, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Small Battery Drive and Small Battery Drive II Adaptor and Light Adaptor by DePuy Synthes: Class I Recall - Possible Explosion Risk, FDA MedWatch
• Medical Device Safety and Recalls: DePuy Synthes Recalls Power Tool System Battery Adaptors Due to Possible Explosion Risk, U.S. Food & Drug Administration (FDA)
• Koffee Kup Bakery, Inc. Voluntarily Recalls Bread Products Due to Possible Presence of Plastic Pieces in Product, U.S. Food & Drug Administration (FDA)
• FDA approves first automated insulin delivery device for type 1 diabetes, U.S. Food & Drug Administration (FDA)
• Café Valley Inc. Issues Allergy Alert on Undeclared (Walnuts) In 12ct Banana Nut Mini Muffins Labeled as 12ct Lemon Poppy Seed Mini Muffins, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - “Healthy” Claim for Food Labeling, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update: FDA Updates Food Facility Registration Product Categories in Guidance, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Updates Food Facility Registration Product Categories in Guidance, U.S. Food & Drug Administration (FDA)
• Urgent Allergy Alert: "Vrindavan" Cow Ghee Recall due to Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• Waymouth Farms, Inc. Issues an Allergy Alert on Undeclared Pecans, Walnuts, Milk and Soy in Good Sense Cranberries 'N More, U.S. Food & Drug Administration (FDA)
• Limited Number of Canned Vegetable Products, Primarily Non-Retail, Recalled for Possible Allergen Risk, U.S. Food & Drug Administration (FDA)
• FDA approves expanded indications for Ilaris for three rare diseases, U.S. Food & Drug Administration (FDA)
• FDA approves Amjevita, a biosimilar to Humira, U.S. Food & Drug Administration (FDA)
• Krishna Food Corp. Recalls Bikaju Chowpati Bhelpuri Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Wells Pharmacy Network Issues Voluntary Nationwide Recall of Sterile Products due to Concern for Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Wells Pharmacy Network Issues Voluntary Nationwide Recall of Sterile Products due to Concern for Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sterile Products by Wells Pharmacy Network: Recall - Concern for Lack of Sterility Assurance, FDA MedWatch
• Blue Bell Ice Cream Recalls Select Products Containing Chocolate Chip Cookie Dough Pieces Purchased From Outside Supplier Aspen Hills Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Be Smoke-free and Help Your Pets Live Longer, Healthier Lives, U.S. Food & Drug Administration (FDA)
• Be prepared for food safety, FoodSafety.gov
• Apple Tree Goat Dairy Recalls Four Goat Cheeses Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Issues Guidance on Veterinary Feed Directive Common Format, U.S. Food & Drug Administration (FDA)
• Time to tailgate!, FoodSafety.gov
• Ferrara Candy Issues Allergy Alert on Undeclared Peanuts and Wheat in Almond Supremes with a Best by Date of 4/22/2017, U.S. Food & Drug Administration (FDA)
• Kellogg Company Recalls Limited Number of Kellogg’s® Eggo® Nutri-Grain® Whole Wheat Waffles Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Mei Shun Noodle, Inc. Issues Allergy Alert on Undeclared Shellfish and Soy in Rice Noodles, U.S. Food & Drug Administration (FDA)
• Censea, Inc. Recalls Shrimp Product Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA HIV Update - Important Labeling Update, U.S. Food & Drug Administration (FDA)
• FDA launches competition to spur innovative technologies to help reduce opioid overdose deaths, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - What to Expect Now that the First Big FSMA Compliance Dates Are Here, U.S. Food & Drug Administration (FDA)
• FDA grants accelerated approval to first drug for Duchenne muscular dystrophy, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Suspends Food Facility Registration of SM Fish Corp., U.S. Food & Drug Administration (FDA)
• FDA permits marketing of balloon device to treat persistent Eustachian tube dysfunction, U.S. Food & Drug Administration (FDA)
• SM Fish Corp Recalls Select Ossie's Ready to Eat Salads Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hyoscyamine sulfate 0.125mg by Virtus Pharmaceuticals: Recall - Superpotent and Subpotent Test Results, FDA MedWatch
• How much food are you wasting?, FoodSafety.gov
• Update of CVM's What's New - Cutting-Edge Technology Sheds Light on Antibiotic Resistance, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Draft Revised Guidance Available, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA to Hold Public Workshop in Oakland, CA to Discuss Menu Labeling, U.S. Food & Drug Administration (FDA)
• FDA protects kids from illegal sales of e-cigarettes, e-liquids and cigars, U.S. Food & Drug Administration (FDA)
• Drew’s, LLC Issues Allergy Alert on Undeclared Milk and Egg in One Lot of Field Day Organic Ranch Dressing, U.S. Food & Drug Administration (FDA)
• Virtus Pharmaceuticals Opco II, LLC Issues Voluntary Nationwide Recall of Hyoscyamine sulfate Due to Superpotent and Subpotent Results, U.S. Food & Drug Administration (FDA)
• Read about Birth Control, Zika and more, FDA Office of Women's Health
• New Seasons Market Issues Allergy Alert on Undeclared Peanuts in Creamy Almond Butter, U.S. Food & Drug Administration (FDA)
• FDA approves VisuMax Femtosecond Laser to surgically treat nearsightedness, U.S. Food & Drug Administration (FDA)
• Are you washing your hands properly?, FoodSafety.gov
• Update of CVM's What's New - FDA Seeks Public Input on Next Steps to Help Ensure Judicious Use of Antimicrobials in Animal Agriculture, U.S. Food & Drug Administration (FDA)
• Shearer’s Foods, LLC Issues Allergy Alert On Undeclared Soy And Milk In No Salt Added Kettle Cooked Potato Chips, U.S. Food & Drug Administration (FDA)
• Publix Recalls Apple Coffee Cakes (Foreign Matter-Metal), U.S. Food & Drug Administration (FDA)
• The September 2016 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GlucaGen HypoKit (glucagon [rDNA origin] for injection) by Novo Nordisk Inc: Recall - Detached Needles on Syringe, FDA MedWatch
• Novo Nordisk Inc. issues voluntary nationwide recall of six batches of GlucaGen® HypoKit® (glucagon [rDNA origin] for injection) due to detached needles on the syringe in the kit, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Provides $21.8 Million to States for Produce Safety, U.S. Food & Drug Administration (FDA)
• FDA provides $21.8 million to states for FSMA produce safety rule implementation, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: The FDA recommends against using screening tests for ovarian cancer screening: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Voluntary Recall of Whole Wheat Flour Product Due to Possible Foreign Matter, U.S. Food & Drug Administration (FDA)
• FDA recommends against using screening tests for ovarian cancer screening, FDA Office of Women's Health
• Food Safety Smarts, FoodSafety.gov
• Update of CVM's What's New - September 2016 Animal Drug Approvals, U.S. Food & Drug Administration (FDA)
• United Exchange Corp Issues Voluntary Nationwide Recall of Family Care Brand Eye Wash Due to Microbial Contamination, U.S. Food & Drug Administration (FDA)
• Island Soups Company, Inc. Recalls Six Varieties of Island Soups Brand Products Because of Possible Contamination With Clostridium Botulinum, U.S. Food & Drug Administration (FDA)
• United Exchange Corp. Issues Voluntary Nationwide Recall of Eye Wash/Eye Irrigating Solutions Distributed by Major Pharmaceuticals and Rugby Laboratories Due to Microbial Contamination, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Draft Guidance on Infant Formula, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Family Care Eye Wash by United Exchange Corp: Recall - Microbial Contamination, FDA MedWatch
• FDA MedWatch - Eye Wash/Eye Irrigating Solutions Distributed by Major Pharmaceuticals and Rugby Laboratories: Recall - Microbial Contamination, FDA MedWatch
• FDA approved changes to the SUSTIVA label, U.S. Food & Drug Administration (FDA)
• FDA approved changes to the GENVOYA, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ovarian Cancer Screening Tests: Safety Communication - FDA Recommends Against Use, FDA MedWatch
• September EdNet: The National Food Safety Educator's Network, FoodSafety.gov
  • <Possible follow-ups>
  • September EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• Westby Cooperative Creamery Issues a Voluntary Product Retrieval Notice on a Specific, Single Production Lot of Cottage Cheese Product, U.S. Food & Drug Administration (FDA)
• DATCP Issues Consumer Advisory for Cottage Cheese Produced By Westby Cooperative Creamery, U.S. Food & Drug Administration (FDA)
• Thermy wants you to help fight bacteria, FoodSafety.gov
• Kanan Enterprises Conducts Voluntary Recall of Cashews with Sea Salt, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Cook Medical Recalls Roadrunner® UniGlide® Hydrophilic Wire Guide Because of Potential Coating Contamination, U.S. Food & Drug Administration (FDA)
• Asher's Chocolates/Lewistown, Inc. Issues Voluntary Recall of Candy Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Wegmans Announces Voluntary Recall for One Date Code of Wegmans Italian Classics Striped Ricotta & Spinach Ravioli, Which May Contain Pieces of White Plastic, U.S. Food & Drug Administration (FDA)
• Kinetic Technologies and Kinetic Vet Announce the Voluntary Nationwide Recall of Hy-Optic, OptiVet and Optimend Due to Deficiencies in Sterility, U.S. Food & Drug Administration (FDA)
• Regalo Bakery Issues Allergy Alert On Undeclared Allergens In Bakery Products, U.S. Food & Drug Administration (FDA)
• FDA allows marketing of clot retrieval devices to reduce disability in stroke patients, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Report on Regional FSMA Import Safety Meetings, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Workshop Registration Reminder, U.S. Food & Drug Administration (FDA)
• FDA issues final rule on safety and effectiveness of antibacterial soaps, U.S. Food & Drug Administration (FDA)
• Aura Cacia Voluntarily Recalls Milk & Oat Bath Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Summit Import Corporation Recalls Yu Yee Brand Black Pepper Powder Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Drug Safety Labeling Changes (SLC) Program now available in new, user-friendly format, FDA MedWatch
• Magic Gourmet Trading Inc. Issues Allergy Alert on Undeclared Allergens in “Koi Palace Mooncakes”, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Mass Spectrometers by Sciex: Safety Communication - Incorrect Assignment of Test Results, FDA MedWatch
• Medical Device Safety and Recalls: FDA Safety Communication: Incorrect Assignment of Test Results Associated with Sciex Mass Spectrometers, U.S. Food & Drug Administration (FDA)
• Do you know where foodborne illness begins?, FoodSafety.gov
• FDA MedWatch - VASCU-GUARD Peripheral Vascular Patch by Baxter International: Letter to Health Care Providers - Potential Risk of Severe Bleeding and Hematomas, FDA MedWatch
• Voluntary Recall of Cartons of Entenmann's Little Bites Fudge Brownies 5 Pack (Best By Date Oct 8, 2016), Chocolate Chip Muffins 5 Pack and 10 Pack (Best By Date Oct 8, 2016) and Variety 20 Pack – Fudge Brownies, Chocolate Chip Muffins and Blueberry Muffins (Best By Date Sep 24, 2016) due to Choking and/or Cutting Hazard from Presence of Small Pieces of Plastic, U.S. Food & Drug Administration (FDA)
• Snyder's-Lance Issues Voluntary Recall of 4oz Diamond of California® Chopped Macadamia Nuts and 2.25oz Diamond of California® Macadamia Halves & Pieces Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Opioid Pain or Cough Medicines Combined With Benzodiazepines: Drug Safety Communication - FDA Requiring Boxed Warning About Serious Risks and Death, FDA MedWatch
• Ton Shen Health/Life Rising Expands Recalls of "DHZC-2 Tablet" to All Lots Purchased Before August 24 2016 Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update: Recalls & Alerts, U.S. Food & Drug Administration (FDA)
• Impax Laboratories, Inc. Issues Voluntary, Nationwide Recall for One Lot of Lamotrigine Orally Disintegrating Tablet 200 mg Due to the Potential for 100 mg Blister Cards being Packaged in 200 mg Containers, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lamotrigine Orally Disintegrating Tablet 200 mg by Impax: Recall - Incorrect Labeling of Blister Cards, FDA MedWatch
• FDA MedWatch - Dietary Supplements by Ton Shen Health/Life Rising: Recall - Elevated Lead Levels, FDA MedWatch
• CFSAN Constituent Update - Comment Period Extension for Draft Guidance to Industry for Voluntarily Reducing Sodium, U.S. Food & Drug Administration (FDA)
• Country Fresh Recalls Product Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Willis Ocean Inc. Issues Allergy Alert on Undeclared Sulfites in Willis Eagle Brand Mut Gung Sweetened Ginger, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Alere Recalls INRatio® and INRatio2® PT/INR Monitoring System Due to Incorrect Test Results, U.S. Food & Drug Administration (FDA)
• FDA advises testing for Zika virus in all donated blood and blood components in the US, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Programmable Syringe Pumps: FDA Safety Communication - Problems With Fluid Flow Continuity at Low Infusion Rates, FDA MedWatch
• FDA Investigates Outbreak of Hepatitis A Illnesses Linked to Raw Scallops, U.S. Food & Drug Administration (FDA)
• Food safety strategies for school lunchtime, FoodSafety.gov
• CFSAN Constituent Update - Three Guidance Documents under FSMA Issued, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Issues Draft Guidances under the FDA Food Safety Modernization Act, 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)
• CFSAN Constituent Update - FDA Extends Certain FSMA Compliance Dates; Issues Draft Guidance, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Announces Grant Award for Tribes and Local Food Producers to Enhance Food Safety and Compliance Under FDA’s Food Safety Modernization Act (FSMA), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Issues Direct Final Rule Revising Categorization of Animal Drugs Used in Medicated Feeds, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Extends Certain FSMA Compliance Dates; Issues Draft Guidance, U.S. Food & Drug Administration (FDA)
• Sage Products Expands Voluntary Worldwide Recall of Specific Lots of Topical Skin Products Due to Potential Microbial Contamination - Second Expansion, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Eyesaline Eyewash by Honeywell: Recall - Microbial Contamination, FDA MedWatch
• Public Workshop: Diabetes Outcome Measures Beyond Hemoglobin A1c, U.S. Food & Drug Administration (FDA)
• Honeywell Issues Voluntary Nationwide Recall Of One Lot Of Eyesaline Eyewash Solution Due To Microbial Contamination, U.S. Food & Drug Administration (FDA)
• Cambridge Farms, LLC Recalls Three Brands Of Frozen Cut Corn Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• New FDA Birth Control Chart, FDA Office of Women's Health
• FDA MedWatch - Oxacillin for Injection, USP, 10g by Sagent: Recall - Iron Oxide Particulate Matter, FDA MedWatch
• Oriental Packing Co. Inc. Issues Alert On Lead In Curry Powder, U.S. Food & Drug Administration (FDA)
• Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of Oxacillin for Injection, USP, 10g Due to Presence of Iron Oxide Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cetylev (acetylcysteine) Effervescent Tablets for Oral Solution: Recall - Inadequate Seal of Blister Pack, FDA MedWatch
• FDA approves expanded indication for two transcatheter heart valves for patients at intermediate risk for death or complications associated with open-heart surgery, U.S. Food & Drug Administration (FDA)
• Bakers of Paris Recalls Croissants Sold at Whole Foods Market Stores in Northern California Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• Voluntary Nationwide Recall of Cetylev® (Acetylcysteine) Effervescent Tablets for Oral Solution Due to an Inadequate Seal of the Blister Pack, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: FDA Recommends Health Care Facilities Stop Using Custom Ultrasonics’ System 83 Plus Automated Endoscope Reprocessors (AERs) for Reprocessing Duodenoscopes; These Reprocessors Remain Available to Reprocess Other Flexible Endoscopes: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Draft Guidance for Industry on Sodium, U.S. Food & Drug Administration (FDA)
• Sage Products Expands Voluntary Nationwide Recall of Comfort Shield Barrier Cream Cloths Due to Microbial Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - System 83 Plus Automated Endoscope Reprocessors by Custom Ultrasonics: FDA Safety Communication - FDA Recommends Stop Using for Reprocessing Duodenoscopes, FDA MedWatch
• Order Free College Health Resources, FDA Office of Women's Health
• Back-to-School Supply Checklist, FoodSafety.gov
• Update of CVM's What's New - FDA Approves Nocita, a New Animal Drug for Local Post-operative Pain in Dogs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Roadrunner UniGlide Hydrophilic Wire Guides by Cook Medical: Recall - Raw Materials Issue, FDA MedWatch
• Cook Medical Issues Global Recall of Roadrunner® UniGlide® Hydrophilic Wire Guides due to raw materials issue, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: BioMerieux SA Alerts Customers about Potential Inaccurate Test Results When using NucliSENS® easyMAG® Magnetic Silica for Nucleic Acid Extraction, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - July 2016 Safety Labeling Changes includes 52 products with revisions to Prescribing Information, FDA MedWatch
• CFSAN Constituent Update - FDA Releases Vending Machine Labeling Guidance Documents, U.S. Food & Drug Administration (FDA)
• Oriental Packing Co., Inc. Issues Alert on Lead in Curry Powder, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - NucliSENS easyMAG Magnetic Silica for Nucleic Acid Extraction by BioMerieux: Recall - Potential Inaccurate Test Results, FDA MedWatch
• FDA MedWatch - DHZC-2 Tablet by Ton Shen Health: Recall - Possible Health Risk, FDA MedWatch
• Ton Shen Health Recalls “DHZC-2 Tablet” Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Issues Final Rule on Food Ingredients that May Be "Generally Recognized as Safe", U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Final Rule on GRAS, U.S. Food & Drug Administration (FDA)
• Rabbit Creek Products recalls certain flavors of bread, muffin and brownie mixes because of a possible health risk, U.S. Food & Drug Administration (FDA)
• FDA updates draft guidance on premarket safety notifications for dietary supplement industry, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Draft Guidance on Premarket Safety Notifications for Dietary Supplements, U.S. Food & Drug Administration (FDA)
• The August 2016 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Read about Sex Differences, Back to School Resources and more, FDA Office of Women's Health
• Country Home Voluntarily Recalls 12- and 24-Count Gourmet Cookies Sold Through ShopRite Stores Fresh Bake Department, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Liquid Drug and Dietary Supplement Products by PharmaTech: Recall - Risk of Product Contamination, FDA MedWatch
• PharmaTech LLC Issues Voluntary Nationwide Recall Due to Potential Risk of Product Contamination, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Current Animal Drug Shortages, U.S. Food & Drug Administration (FDA)
• Update: Gel Spice, Inc. Issues Expanded Recall of Ground Tumeric Powder Due to Elevated Lead Levels, U.S. Food & Drug Administration (FDA)
• Beyond Better Foods, LLC Issues Allergy Alert On Undeclared Peanuts In Mislabeled Peanut Butter Chocolate Chip Ice Cream, U.S. Food & Drug Administration (FDA)
• Update: JM Exotic Foods, Inc. Recalls Ground Turmeric Due to Elevated Levels of Lead, U.S. Food & Drug Administration (FDA)
• Hospira Issues a Voluntary Nationwide Recall For One Lot Of 0.25% Bupivacaine Hydrochloride Injection, USP Due to The Presence Of Particulate Matter Within a Single Vial, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 0.25% Bupivacaine Hydrochloride Injection, USP by Hospira: Recall - Particulate Matter, FDA MedWatch
• Update of CVM's What's New - FDA Releases Final Environmental Assessment for Genetically Engineered Mosquito, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - VentStar Oxylog 3000 Pediatric Patient Breathing Circuit by Dräger: Class I Recall - Potential Valve Leakage, FDA MedWatch
• Medical Device Safety and Recalls: Dräger Recalls VentStar Oxylog 3000 Pediatric Patient Breathing Circuit, U.S. Food & Drug Administration (FDA)
• Grassfields Cheese LLC Issues Nationwide Voluntary Recall Of Certain Cheeses, U.S. Food & Drug Administration (FDA)
• JML Ingredients Recalls IQF Cut Green Beans Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• JM Exotic Foods, Inc. Recalls Ground Turmeric Due to Elevated Levels of Lead, U.S. Food & Drug Administration (FDA)
• Mann Packing Voluntarily Issuing Class 1 Recall Of O Organics Organic Vegetable Tray With Creamy Ranch Dressing Dip Due To Mislabeled Ingredients That May Pose An Allergen Risk, U.S. Food & Drug Administration (FDA)
• Grassfields Cheese Recall Affects Select Whole Foods Market Locations; Grocer Recalls Product from Cheese Departments, U.S. Food & Drug Administration (FDA)
• Teva Pharmaceuticals Initiates Voluntary Nationwide Recall of Seven Lots of Amikacin Sulfate Injection USP 500 mg/2 mL (250 mg/mL) and 1 Gram/4 mL (250 mg/mL) Vials Due to Potential of Glass Particulate Matter, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - August 2016 Animal Drug Approvals, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Provides Information to Assist Industry with New Nutrition Facts Label, U.S. Food & Drug Administration (FDA)
• August 2016 EdNet: The National Food Safety Educator's Network, FoodSafety.gov
• FDA MedWatch - Amikacin Sulfate Injection USP 500 mg/2 mL (250 mg/mL) and 1 Gram/4 mL (250 mg/mL) Vials by Teva: Recall - Glass Particulate Matter, FDA MedWatch
• Sage Products Issues Voluntary Nationwide Recall of Comfort Shield Barrier Cream Cloths Due to Microbial Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Comfort Shield Barrier Cream Cloths by Sage Products: Recall - Product Contamination, FDA MedWatch
• Hampton Creek Issues Voluntary Recall of Mixes Containing Native Forest Coconut Milk Powder Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Allergen Alert Expansion: Kitchen Cravings Strawberry and Mixed Berry Parfaits with Trace Peanuts or Almonds, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - August 1, 2016, U.S. Food & Drug Administration (FDA)
• SM Fish Corp Recalls Select Ossie's Ready To Eat Herring Salads Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Updated: Additional Package Codes Of Watts Brothers Farms Organic Mixed Vegetables, Organic Super Sweet Corn, and Organic Peas Recalled Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Blog: Busting 5 Common Myths about FDA and Women's Health, FDA Office of Women's Health