FDA News Releases

• Date Index

• Atkins Nutritional, Inc. Voluntary Recalls Limited Quantity of Atkins Chocolate Candies, U.S. Food & Drug Administration (FDA)
• H-E-B Issues Voluntary Recall H-E-B hamburger and hotdog buns and Hill Country Fare hotdog buns recalled for quality issues., U.S. Food & Drug Administration (FDA)
• Grand BK Corp. Recalls Goodies By Nature Raw Cashews, Net Wt. 9oz Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 24, 2015, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Voluntarily Recalls Packaged Raw Macadamia Nuts Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Summer e-Update: Women's Health Highlights from FDA Office of Women's Health, FDA Office of Women's Health
• Update of CVM's What's New - Medicated Feed Labeling for Manufacturers – Getting it Right, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Daytrana Patch (methylphenidate transdermal system): Drug Safety Communication - Permanent Skin Color Changes, FDA MedWatch
• FDA MedWatch - Covidien Shiley Neonatal and Pediatric Tracheostomy Tubes by Medtronic: Recall - Tubes Formed With Wider-angle Bend Than Standard Models, FDA MedWatch
• Wish-Bone Salad Dressing Issues Allergy Alert on Undeclared Egg in 24 oz. Wish-Bone Ranch Salad Dressing, U.S. Food & Drug Administration (FDA)
• Good Seed Inc. Recalls Soybean Sprouts and Mung Bean Sprouts Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• La Mexicana Announces the Recall of Spinach Dip for Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Medtronic Implements Worldwide Voluntary Recall for Certain Lots of Neonatal and Pediatric Tracheostomy Tubes, U.S. Food & Drug Administration (FDA)
• Checklist for the Perfect Summer Picnic, FoodSafety.gov
• Project 7 Issues Allergy Alert on Undeclared Milk/Dairy Ingredient In Sour Caramel Apple Gum, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Final Rule on Infant Formula, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: HeartWare Ventricular Assist System – Updated with Multiple Reasons for Recall, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Boulder Dog Food Company, L.L.C. Voluntarily Recalls Ten Bags of Chicken Sprinkles, U.S. Food & Drug Administration (FDA)
• United Salad Co. Recalls Champ's Sliced Crimini Mushrooms Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Boulder Dog Food Company, L.L.C. Voluntarily Recalls Ten Bags of Chicken Sprinkles, 3 oz. With A “Best By” Date of “05/04/16” Due to Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 17, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - M/L Taper with Kinectiv Technology Prosthesis by Zimmer: Class I Recall - Higher than Expected Levels of Manufacturing Residues, FDA MedWatch
• Medical Device Safety and Recalls: Zimmer M/L Taper with Kinectiv Technology Prosthesis Femoral Stems and Necks - Higher than Expected Levels of Manufacturing Residues, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces New Grant Funding Opportunity to Support Development of New Animal Drugs Intended for Minor Use or Minor Species, U.S. Food & Drug Administration (FDA)
• The Raymond-Hadley Corporation Issues Allergy Alert on Undeclared Sulfites in Phoebe Mote Blanco White Corn Semoule De Mais Blanc, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Guidance for Industry on Allergens, U.S. Food & Drug Administration (FDA)
• Nuevo sitio en español sobre temas de salud para toda la familia, GobiernoUSA.gov
• 10 consejos para el uso de fuegos artificiales este Cuatro de Julio, GobiernoUSA.gov
• FDA MedWatch - HeartWare Ventricular Assist System: Class I Recall - Damaged Alignment Guides or Connection Pins May Cause Pump to Stop, FDA MedWatch
• Medical Device Safety and Recalls: HeartWare Ventricular Assist System - Damaged Alignment Guides / Connection Pins May Cause Pump to Stop, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Potiga (ezogabine): Drug Safety Communication - FDA Determines 2013 Labeling Adequate to Manage Risks of Retinal Abnormalities, Potential Vision Loss, and Skin Discoloration, FDA MedWatch
• Make Food Safety Part of Your Father's Day, FoodSafety.gov
• CFSAN Constituent Update - Removing Trans Fat, U.S. Food & Drug Administration (FDA)
• G&C Natural Nutrition, Inc. Issues Voluntary Nationwide Recall of Pyrola Due to Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - May 2015 Safety Labeling Changes includes 43 products with revisions to Prescribing Information, FDA MedWatch
• Philips Response To ResMed Update On Phase IV SERVE-HF Study Of Adaptive Servo-Ventilation (ASV) Therapy In Central Sleep Apnea And Chronic Heart Failure, U.S. Food & Drug Administration (FDA)
• Wisconsin Firm Voluntarily Recalls Potato Salad Due to the Possible Presence of Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Cyclosporiasis is More Common in the Summer - Learn More, FoodSafety.gov
• CVM Updates - Final Guidances Available, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CVM Updates - Final Guidances Available, U.S. Food & Drug Administration (FDA)
• Natural Grocers® expands recall of Macadamia Nuts due to possible health risk, U.S. Food & Drug Administration (FDA)
• Walgreen Co. Recalls Product Because of Possible Mold Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 10, 2015, U.S. Food & Drug Administration (FDA)
• ¿Cómo una persona se convierte en donante de órganos?, GobiernoUSA.gov
• Update of CVM's What's New - FDA Research Helps Keep Pets and Humans Safe, U.S. Food & Drug Administration (FDA)
• Listeria: The Unwanted BBQ Guest, FoodSafety.gov
• Update of CVM's What's New - Reopening of Comment Period: Identification of Alternative In Vitro Bioequivalence Pathways, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Injectable Products by Mylan: Recall - Presence of Particulate Matter - UPDATE, FDA MedWatch
• Mylan is Expanding its Voluntary Nationwide Recall of Select Lots of Injectable Products Due to the Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• The June 2015 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Ainsworth Pet Nutrition Voluntarily Recalls Five Nutrish® Wet Cat Food Varieties, U.S. Food & Drug Administration (FDA)
• Santa Barbara Smokehouse Voluntary Recalls Cold Smoked Salmon Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Ainsworth Pet Nutrition Voluntarily Recalls Five Nutrish&reg; Wet Cat Food Varieties For Potentially Elevated Vitamin D Levels, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Baxter Healthcare, VASCU-GUARD Peripheral Vascular Patch - May Cause Blood Clots, U.S. Food & Drug Administration (FDA)
• Best Cash & Carry is Voluntarily Recalling Green Raisins (Sunderkhani) Because They May Contain Undeclared Sulfites, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 03, 2015, U.S. Food & Drug Administration (FDA)
• SmartLipo365 Issues Voluntary Nationwide Recall of Smart Lipo Due to Undeclared Sibutramine, Desmethylsibutramine, and Phenolphthalein, U.S. Food & Drug Administration (FDA)
• Dr. Praeger’s Sensible Foods Issues Allergy Alert for Gluten Free California Veggie Burger Due to Undeclared Soy, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Updat: Draft Guidance for Industry: FDA's Voluntary Qualified Importer Program, U.S. Food & Drug Administration (FDA)
• Frontiere Natural Meats, LLC Recalls Ground Elk Meat Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - New FDA Program Will Benefit Both Importers and Consumers, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vascu-Guard Peripheral Vascular Patch by Baxter: Recall - Difficulty Distinguishing the Smooth from Rough Surface, FDA MedWatch
• Update of CVM's What's New - CVM Issues Assignment to Collect Official Samples of Raw Foods for Dogs or Cats, U.S. Food & Drug Administration (FDA)
• Baxter Initiates Voluntary Recall of Select Product Codes of Peripheral Vascular Patch, U.S. Food & Drug Administration (FDA)
• Cómo prepararse para viajar en avión con su mascota, GobiernoUSA.gov
• Update of CVM's What's New - Animal Drug Approvals June 2015 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Road Rules for Food Safety, FoodSafety.gov
• CVM Updates - FDA Regulation to Help Ensure Judicious Use of Antibiotics in Food-Producing Animals, U.S. Food & Drug Administration (FDA)
• The Hemisphere Group, Inc. Recalls Vietnamese LP Cashews Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated FSMA and Animal Feed, U.S. Food & Drug Administration (FDA)
• Paleteria La Jalpita Issues Allergy Alert On Undeclared Milk And Sulfite In Ice Cream Bars And Popsicles, U.S. Food & Drug Administration (FDA)
• The Popcorn Factory, Inc. Issues Allergy Alert on Undeclared Milk in Product, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 27, 2015, U.S. Food & Drug Administration (FDA)
• Mes de la Salud Mental: ayuda para veteranos, GobiernoUSA.gov
• FDA approves new drug to treat rare lung disease that primarily affects women, FDA Office of Women's Health
• CVM Updates - FDA Releases Draft Guidance for Animal Drug Sponsors Determining an Acute Reference Dose (ARfD), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Unintentional Injection of Soft Tissue Filler into Blood Vessels in the Face: FDA Safety Communication - Risk of Serious Patient Injury, FDA MedWatch
• FDA Safety Communication: Unintentional Injection of Soft Tissue Filler into Blood Vessels in the Face, FDA Office of Women's Health
• Donaciones a organizaciones cartitativas: sepa cómo reportar estafas, GobiernoUSA.gov
• Medical Device Safety and Recalls: Unintentional Injection of Soft Tissue Filler into Blood Vessels in the Face: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Euro Import Distributions Inc Issues an Alert on Undeclared Sulfites in Dried Apricots, U.S. Food & Drug Administration (FDA)
• Bedessee Imports Inc., Voluntarily Recalls Brown Betty Coconut Milk Powder Due to Presence of Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Natural Grocers® issues recall of Macadamia Nuts due to possible health risk, U.S. Food & Drug Administration (FDA)
• Carefusion Provides Update on Voluntary Global Recall of Avea® Ventilator, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Avea Ventilator by CareFusion: Recall - Potential Malfunction of Pressure Transducer, FDA MedWatch
• Food Safety for Power Outages, FoodSafety.gov
• Jose Madrid Salsa Issues Voluntary Recall, U.S. Food & Drug Administration (FDA)
• House of Spices (India) Inc. Issues Alert on Undeclared Sulfites in "Dry Apricot", U.S. Food & Drug Administration (FDA)
• Whole Foods Market's Oakland Store Voluntarily Recalls Jivara Lactee Milk Chocolate Valrhona Cut and Wrap Pieces Due to Undeclared Tree Nut Allergen, U.S. Food & Drug Administration (FDA)
• Falcon Trading Company, Inc. dba SunRidge Farms Is Voluntarily Recalling Coconut-Medium Shred Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Falcon Trading Company, Inc. dba SunRidge Farms is Voluntarily Recalling Vanilla Candy-Coconut Chews Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Advertencia de seguridad para unos 34 millones de vehículos, GobiernoUSA.gov
• Enforcement Report for May 20, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Zerbaxa (ceftolozane and tazobactam): Drug Safety Communication - FDA Cautions about Dose Confusion and Medication Errors, FDA MedWatch
• Seminario virtual sobre acción diferida (DACA) HOY a las 3:30 PM, hora del Este, GobiernoUSA.gov
• Comparta su estilo de vida saludable, GobiernoUSA.gov
• A&S Food Trading Inc. Issues an Alert on Undeclared Sulfites in Hua Zhi Ying Brand Gourd Candy, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Releases Proposed Rule to Collect Antimicrobial Sales and Distribution Information by Animal Species, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Releases Draft Guidance on Animal Drug Compounding from Bulk Drug Substances, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - OC Raw Dog Recalls Turkey & Produce Raw Frozen Canine Formulation Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Natural Creations Issues Allergy Alert on Undeclared Milk Ingredient in Dietary Supplement New Zealand Colostrum, U.S. Food & Drug Administration (FDA)
• Aurora Products, Inc. Announces Voluntarily Recall of Aurora Natural Brand and Certain Private Label Branded Raw Macadamia Nuts Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• OC Raw Dog Recalls Turkey & Produce Raw Frozen Canine Formulation Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - SGLT2 inhibitors: Drug Safety Communication - FDA Warns Medicines May Result in a Serious Condition of Too Much Acid in the Blood, FDA MedWatch
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update Recalls & Alerts, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Vulnerabilities of Hospira LifeCare PCA3 and PCA5 Infusion Pump Systems: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 13, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - LifeCare PCA3 and PCA5 Infusion Pump Systems by Hospira: FDA Safety Communication - Security Vulnerabilities, FDA MedWatch
• ¡Ayúdenos a mejorar el nuevo GobiernoUSA.gov!, GobiernoUSA.gov
• FDA MedWatch - April 2015 Safety Labeling Changes includes 55 products with revisions to Prescribing Information, FDA MedWatch
• HIV/AIDS Update - Draft Blood donor deferral policy for men who have had sex with another man (MSM), U.S. Food & Drug Administration (FDA)
• FDA Office of Women's Health May 2015 e-Update, FDA Office of Women's Health
• CVM Updates - FDA Issues Final Guidance on Veterinary Drug Genotoxicity Testing, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses/VFD Distributor Notifications, U.S. Food & Drug Administration (FDA)
• CONSUMER ALERT: Undeclared Peanuts in "Cumin Powder", U.S. Food & Drug Administration (FDA)
• Good Seed Inc. Recalls Soybean Sprouts & Mung Bean Sprouts Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals May 2015 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 06, 2015, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Guidance for Industry 191, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Maquet Medical Systems, Tiger Paw System II - May Cause Tears and Bleeding in Heart Tissue, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tiger Paw System II by Maquet Medical Systems: Class I Recall - May Cause Tears and Bleeding in Heart Tissue, FDA MedWatch
• CVM Updates - Draft Guidance on Mandatory Food Recalls Available for Comment, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Kent Nutrition Group, Inc. Initiates Recall of Poultry Feed, U.S. Food & Drug Administration (FDA)
• Golden Krust Caribbean Bakery & Grill Issues Allergy Alert on Undeclared Egg in Jamaican Style Shrimp and Soya Patties, U.S. Food & Drug Administration (FDA)
• The May 2015 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Draft Guidance on Mandatory Food Recalls, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Adrucil (fluorouracil Injection, USP) 5 g/100 mL (50 mg/mL): Recall - Particulate Matter, FDA MedWatch
• Kent Nutrition Group, Inc. Initiates Recall of Poultry Feed, U.S. Food & Drug Administration (FDA)
• Teva Parenteral Medicines Initiates Voluntary Nationwide Recall of Select Lots of Adrucil® (fluorouracil Injection, Usp) 5 G/100 Ml (50 Mg/ml) Due to Particulate Matter, U.S. Food & Drug Administration (FDA)
• Poco Dolce Confections Announces Recall of Individually Wrapped Tile Varieties: Almond, Aztec Chile, Burnt Caramel, Almond Coconut, Ginger, and Sesame Toffee, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - FDA considerations for a revised blood donor deferral policy, U.S. Food & Drug Administration (FDA)
• Donación de órganos y tejidos para una segunda vida, GobiernoUSA.gov
• FDA Veterinarian - May 1, 2015, U.S. Food & Drug Administration (FDA)
• FDA approves Raplixa to help control bleeding during surgery, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Mammograms at Coastal Diagnostic Center in Pismo Beach, California: FDA Safety Communication - Quality Problems, FDA MedWatch
• FDA Safety Communication: Problem with Quality of Mammograms at Coastal Diagnostic Center in Pismo Beach, California, U.S. Food & Drug Administration (FDA)
• CVM Updates- FDA Seeks Public Comment on Risk Assessment of Drug Residues in Milk and Milk Products, U.S. Food & Drug Administration (FDA)
• Voluntary Recall for Navajo Pride Bleached Flour Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 29, 2015, U.S. Food & Drug Administration (FDA)
• Hy-Vee Recalls Summer Fresh Pasta Salad, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Seeks Public Comment on Risk Assessment Related to Milk, U.S. Food & Drug Administration (FDA)
• FDA approves first generic Abilify to treat mental illnesses, U.S. Food & Drug Administration (FDA)
• Waymouth Farms, Inc. Recalls Raw Pine Nuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA enters consent decree with Medtronic, Inc., U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Letter on Fluoride Added to Bottled Water, U.S. Food & Drug Administration (FDA)
• Greystone Foods, LLC voluntarily recalls Today’s Harvest Field Peas with Snaps, Silver Queen Corn, and Broccoli Florets due to possible health risk., U.S. Food & Drug Administration (FDA)
• TFH Publications, Inc./Nylabone Products Recalls Puppy Starter Kit Due To Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - TFH Publications, Inc./Nylabone Products Recalls Puppy Starter Kit Due To Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Large Volume Intravenous (IV) Solution Shortage, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Injectable Products by Mylan: Recall - Presence of Particulate Matter, FDA MedWatch
• Mylan Initiates Voluntary Nationwide Recall of Select Lots of Injectable Products Due to the Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• Sweet Sam's Baking Company Issues Allergy Alert on Undeclared Milk in Starbucks Black & White Mini Cookies, U.S. Food & Drug Administration (FDA)
• Jeni's Splendid Ice Creams Recalls All Products Because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Bupivacaine HCl Injection by Hospira: Recall - Iron Oxide Particulate In Glass Vials, FDA MedWatch
• Inventure Foods, Inc. Issues Voluntary Recall of Its Fresh Frozen Vegetables and Select Jamba "At Home" Smoothie Kits Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Hospira Issues A Voluntary Nationwide Recall Of One Lot Of Bupivacaine HCl Injection, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Letter to Veterinarians Regarding FERTAGYL, U.S. Food & Drug Administration (FDA)
• Hospira Issues A Voluntary Nationwide Recall Of One Lot Of Bupivacaine HCl Injection Due To Potential Iron Oxide Particulate In Glass Vials, U.S. Food & Drug Administration (FDA)
• Inventure Foods, Inc. Issues Voluntary Recall of its Fresh Frozen Vegetables and Jamba "At Home" Smoothie Kits Because of Possible Heath Risk, U.S. Food & Drug Administration (FDA)
• FDA Webinar: April 27: Drug Trials Snapshots Initiative, U.S. Food & Drug Administration (FDA)
• Illinois food company agrees to stop production of contaminated sprouts, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - The FDA Science Forum, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: LuSys Laboratories, Inc., Ebola Virus One-Step Test Kits - Not Cleared for Marketing, U.S. Food & Drug Administration (FDA)
• SM Fish Corp. Issues Allergy Alert On Undeclared Eggs In Ossies Pickled Lox & Cream, U.S. Food & Drug Administration (FDA)
• SM Fish Corp. Issues Allergy Alert On Undeclared Milk In Ossies Herring In Sourcream And Ossie’s Pickled Lox Dairy Products, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 22, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Mucinex Fast-MAX Products: Recall - Incorrect Labeling, FDA MedWatch
• Celebre el Día del Planeta Tierra, GobiernoUSA.gov
• CONSUMER ALERT: STAPHYLOCOCCUS AUREUS IN QUESO FRESCO CHEESE, U.S. Food & Drug Administration (FDA)
• Blue Bell Creameries Voluntarily Expands Recall to Include All of its Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Royal Frozen Food Recalls Blintzes Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Superior Nut & Candy Co., Inc. Recalls Pine Nuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Laying the Foundation for FSMA Implementation: Questions and Answers with Roberta Wagner and Joann Givens, U.S. Food & Drug Administration (FDA)
• Prolainat Voluntarily Recalls Trader Joe’s A Dozen Sweet Bites Due to Undeclared Coconut, U.S. Food & Drug Administration (FDA)
• Hines Nut Company Voluntary WALNUT HALVES AND PIECES Due to Possible Health Risk Recalls, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Voluntarily Recalls Packaged Raw Macadamia Nuts Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Conway Import Co., Inc. is Voluntarily Recalling Conway Organic Sesame Ginger Dressing and Conway Citrus Organic Vinaigrette Dressing Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Ingeniería genética en los alimentos, GobiernoUSA.gov
• FDA MedWatch - Flurbiprofen-Containing Topical Pain Medications: FDA Alert - Illnesses and Deaths in Pets Exposed to Prescription Topical Pain Medication, FDA MedWatch
• Update of CVM's What's New - 2014 Annual Report to Congress on the Use of Mandatory Recall Authority Available, U.S. Food & Drug Administration (FDA)
• Schnucks Recalls Chef’s Express California Pasta Salad Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Warns of Illnesses and Deaths in Pets Exposed to Prescription Topical Pain Medications Containing Flurbiprofen, U.S. Food & Drug Administration (FDA)
• Smiths Food and Drug Stores recall In-store Bakery Carrot Cake, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 15, 2015, U.S. Food & Drug Administration (FDA)
• Tres alimentos altamente beneficiosos para la salud, GobiernoUSA.gov
• FDA approves first generic Copaxone to treat multiple sclerosis, U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize unapproved drugs from Florida distributor, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Meeting Materials Available for the April 23-24 FSMA Public Meeting, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - VV13F Reinforced Dual Lumen ECMO Catheters by OriGen Biomedical: Recall - Potential for Separation of Tube from Hub, FDA MedWatch
• Solutions At Work, Inc. Issues Allergy Alert On Undeclared Raw Cashews In Cleveland Crops Chili Cheezy Kale Chips, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update: Warning Letters Citing Color Additive Violations, U.S. Food & Drug Administration (FDA)
• FDA approved changes to the Olysio (simeprevir) package insert, U.S. Food & Drug Administration (FDA)
• OriGen Biomedical Issues Nationwide Recall of OriGen VV13F Reinforced Dual Lumen ECMO Catheters, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update John Frieda Beach Blonde Sun Streaks Lightening Spray 3.5 Fl. Oz. Recalled Due to Defective Peel-out Labels, U.S. Food & Drug Administration (FDA)
• FDA approves Corlanor to treat heart failure, U.S. Food & Drug Administration (FDA)
• April 2015 FDA Office of Women's Health Update, FDA Office of Women's Health
• CVM Updates - Updated FDA Releases 2012 NARMS Retail Meat Annual Report, 2013 Preliminary Data; Some Encouraging Early Trends Seen, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - March 2015 Safety Labeling Changes includes 67 products with revisions to Prescribing Information., FDA MedWatch
• Undeclared Peanuts in “Cumin Powder”, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Encourages Comments to Help Update Food Ingredient Safety Assessment (Redbook), U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Addressing the Shortage of Large Volume Intravenous Solutions, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Releases 2012 NARMS Retail Meat Annual Report, 2013 Preliminary Data; Some Encouraging Early Trends Seen, U.S. Food & Drug Administration (FDA)
• FDA Safety Notification: Problem with Quality of Mammograms at J. Bruce Jacobs M.D., Inc., doing business as Huntington Radiology in Huntington Park, California, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Clarifies Draft Guidance for Safety of Animal Feed on the Farm, U.S. Food & Drug Administration (FDA)
• La Guadalupana to Voluntary Recall Some of its Shelf Food Products from Illinois, Wisconsin and Indiana Stores, U.S. Food & Drug Administration (FDA)
• Retiro Voluntario del Mercado de Algunos Productos La Guadalupana en Comercios de Illinois, Wisconsin e Indiana, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 08, 2015, U.S. Food & Drug Administration (FDA)
• Blood, Vaccines and Other Biologics Advisory Committees, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Blood, Vaccines and Other Biologics Advisory Committees, U.S. Food & Drug Administration (FDA)
  • Blood, Vaccines and Other Biologics Advisory Committees, U.S. Food & Drug Administration (FDA)
  • Blood, Vaccines and Other Biologics Advisory Committees, U.S. Food & Drug Administration (FDA)
  • Blood, Vaccines and Other Biologics Advisory Committees, U.S. Food & Drug Administration (FDA)
  • Blood, Vaccines and Other Biologics Advisory Committees, U.S. Food & Drug Administration (FDA)
  • Blood, Vaccines and Other Biologics Advisory Committees, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Intravenous (IV) Solutions (Select Lots) by Baxter: Recall - Potential Presence of Particulate Matter, FDA MedWatch
• Update of CVM's What's New - FDA to Industry: Let’s Increase the Availability of Safe, Effective Animal Drugs, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Annual Summary Report on Antimicrobials Sold or Distributed in 2013 for Use in Food-Producing Animals, U.S. Food & Drug Administration (FDA)
• Baxter Initiates Voluntary Recall of Select Lots of IV Solutions Due to the Potential Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• Kanan Enterprises Conducts Nationwide Voluntary Recall of Macadamia Nuts, U.S. Food & Drug Administration (FDA)
• Texas Pecan Company Voluntarily Recalls Macadamia Nuts and Products Containing Macadamia Nuts Because of Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• A Chicken Beat A Bear..., FoodSafety.gov
• World Wide Gourmet Foods Issues Allergy Alert on Undeclared Wheat and Soy in Central Market Teriyaki Salmon Jerky, U.S. Food & Drug Administration (FDA)
• Sabra Dipping Company Issues Nationwide Voluntary Recall of Select SKUs of Its Classic Hummus, U.S. Food & Drug Administration (FDA)
• Únase al programa escolar “Almuerzo libre de desechos”, GobiernoUSA.gov
• Texas Star Nut and Food Co., Inc. Expands Its Voluntary Recall to Include Additional Macadamia Nut Products Due to Recall Notification From Their Supplier of Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Proposes to Amend Regulation on Registration of Food Facilities, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Proposed Rule for Food Facility Registration, U.S. Food & Drug Administration (FDA)
• Blue Bell Creameries Expands Recall of Products Produced in Broken Arrow, Oklahoma Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Best Foods Inc. Issues Allergy Alert on Undeclared Peanuts in Deer Cumin Powder 7 Ounce and Deer Cumin Powder 14 Ounce, U.S. Food & Drug Administration (FDA)
• CVM Updates - Approval Withdrawn for Antifreeze Antidote for Dogs, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listings of Medicated Feed Mill Licenses/VFD Distributor Notifications, U.S. Food & Drug Administration (FDA)
• Henry’s Farm Inc Recalls Soybean Sprouts Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• #foodsafety=World Health Day 2015, FoodSafety.gov
• Update of CVM's What's New - Animal Drug Approvals April 2015 Update (Green Book), U.S. Food & Drug Administration (FDA)
• The April 2015 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• North Carolina Board of Pharmacy Announces a Recall of All Lots of Non- Sterile and Sterile Products Compounded, Repackaged, and Distributed by Prescription Center Between September 10, 2014 and March 10, 2015 Due to Lack of Sterility, Potency, and Stability Assurance, U.S. Food & Drug Administration (FDA)
• Maya Overseas Food Inc. Issues Allergy Alert on Undeclared Peanuts in “Cumin Powder”, U.S. Food & Drug Administration (FDA)
• La Terra Fina Expands Voluntary Product Recall to Include a Single Lot of Its 10-Ounce Chunky Spinach Artichoke & Parmesan Dip & Spread, Due to Supplier Recall of Organic Spinach, U.S. Food & Drug Administration (FDA)
• Raja Foods Issues Allergy Alert on Undeclared Peanuts in "Swad Cumin Powder 14 Oz", U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 01, 2015, U.S. Food & Drug Administration (FDA)
• El Gobierno invita al público a definir lo que es una dieta saludable, GobiernoUSA.gov
• FDA MedWatch - Products from Prescription Center Pharmacy in Fayetteville, N.C.: Recall - Lack of Sterility Assurance, FDA MedWatch
• CVM Updates - FDA Alerts Veterinarians and Pet Owners Not to Use Prescription Center Pharmacy Products, U.S. Food & Drug Administration (FDA)
• New USDA ‘FoodKeeper’ App: Your New Tool for Smart Food Storage, FoodSafety.gov
  • <Possible follow-ups>
  • New USDA ‘FoodKeeper’ App: Your New Tool for Smart Food Storage, FoodSafety.gov
• FDA alerts health care professionals and patients not to use products from the Prescription Center pharmacy in Fayetteville, N.C., U.S. Food & Drug Administration (FDA)
• CVM Updates - New FDA Animal Drug Product Guidance Now Available, U.S. Food & Drug Administration (FDA)
• Cómo reportar productos que son un riesgo para usted, GobiernoUSA.gov
  • <Possible follow-ups>
  • Cómo reportar productos que son un riesgo para usted, GobiernoUSA.gov
• Giant Eagle Voluntarily Recalls Multiple Items Due to Undeclared Egg and Milk Allergens, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Pending Withdrawal of Approval of Nitarsone, U.S. Food & Drug Administration (FDA)
• FDA issues final guidance on the evaluation and labeling of abuse-deterrent opioids, U.S. Food & Drug Administration (FDA)
• GetGo from Giant Eagle Voluntarily Recalls Select Grab-and-Go Subs Due to an Undeclared Egg Allergen, U.S. Food & Drug Administration (FDA)
• Whole Foods Market's Southwest Region Recalls Bran Muffin Six Packs Due To Undeclared Egg And Milk, U.S. Food & Drug Administration (FDA)
• Hannaford Announces Recall of Two Mixed Nut Items, U.S. Food & Drug Administration (FDA)
• Aurora Products, Inc. Expands Voluntary Product Recall to Include One Additional Private Label Branded Customer and to Clarify the Name of Two Bulk Products Previously Recalled That Used Walnuts in Them Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - New Funding Opportunity Announcement for Minor Use/Minor Species (MUMS) Development of Drugs, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Compliance Program Guide 7368.001 – Pre-Approval Inspections, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Feraheme (ferumoxytol): Drug Safety Communication – Warnings Strengthened and Prescribing Instructions Changed, FDA MedWatch
• CVM Updates - FDA Issues Guidance for Target Animal Safety Data Presentation, U.S. Food & Drug Administration (FDA)
• Aurora Products, Inc. Expands Voluntary Product Recall to Include Certain Private Label Branded Walnut and Trail Mix Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Best Foods Inc. Issues Alert on Undeclared Sulfites in Deer Brand Raisin Golden, U.S. Food & Drug Administration (FDA)
• Silver Lake Cookie Company, Inc. Issues Allergy Alert On Undeclared Eggs In "Easter Egg Cookies", U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Index of Legally Marketed Unapproved New Animal Drugs for Minor Species, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Index of Legally Marketed Unapproved New Animal Drugs for Minor Species, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA and AAFCO Extend MOU to Facilitate the Animal Food Ingredient Definition Request Process, U.S. Food & Drug Administration (FDA)
• CVM Updates - The FDA Announces Strategy to Create Definitions and Standards for Animal Food Ingredients, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 25, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Duodenoscope Model TJF-Q180V by Olympus: FDA Safety Communication - New Reprocessing Instructions Validated, FDA MedWatch
• Medical Device Safety and Recalls: Olympus Validates New Reprocessing Instructions for Model TJF-Q180V Duodenoscopes, U.S. Food & Drug Administration (FDA)
• La Terra Fina Recalls Various Products Due to Supplier Recall of Organic Spinach, U.S. Food & Drug Administration (FDA)
• Recomendaciones para evitar accidentes en los cruces de ferrocarril, GobiernoUSA.gov
• Reduzca sus impuestos por el cuidado de niños y dependientes, GobiernoUSA.gov
• Lindt USA Issues Allergy Alert on Undeclared Hazelnuts in Chocolate Covered Raisin and Chocolate Covered Almond Bags, U.S. Food & Drug Administration (FDA)
• FDA approves new treatment for diabetic retinopathy in patients with diabetic macular edema, U.S. Food & Drug Administration (FDA)
• FDA approves treatment for inhalation anthrax, U.S. Food & Drug Administration (FDA)
• Superior Foods, Inc., of Watsonville, CA is recalling 8,475 Cases Of Simply Balanced 10-oz Frozen Organic Chopped Spinach Distributed Exclusively At Target Stores., U.S. Food & Drug Administration (FDA)
• Twin City Foods, Inc. Recalls Frozen Cadia Organic Cut Spinach, Meijer Organics Chopped Spinach, Wild Harvest Organic Cut Leaf Spinach, and Wegmans Organic Just Picked Spinach Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
• FDA approved revisions to the Epivir (lamivudine) and Ziagen (abacavir sulfate) labels, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Mammograms at Richard D. Adelman M.D. in Raleigh, North Carolina: FDA Safety Communication - Quality Problems, FDA MedWatch
• Medical Device Safety and Recalls: Problems with Quality of Mammograms at Richard D. Adelman M.D. in Raleigh, North Carolina: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Supervalu Inc. Issues Allergy Alert on Undeclared Peanuts in Product, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hepatitis C Treatments Containing Sofosbuvir in Combination With Another Direct Acting Antiviral Drug: Drug Safety Communication - Serious Slowing of Heart Rate When Used With Antiarrhythmic Drug Amiodarone, FDA MedWatch
• Giant Eagle Voluntarily Recalls Japanese Breaded Cod Fillets Due to an Undeclared Soy Allergen, U.S. Food & Drug Administration (FDA)
• Giant Eagle Voluntarily Recalls Little Italy Paninis Due to an Undeclared Egg Allergen, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - FDA Drug Safety Communication re: Harvoni and Sovaldi, U.S. Food & Drug Administration (FDA)
• Carmel Food Group Recalls Rising Moon Organics Frozen Ravioli Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Blue Bell Ice Cream Recalls 3 oz. Institutional/Food Service Ice Cream Cups – Chocolate, Strawberry, Vanilla (Tab Lid) – Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves blood pump system to help patients maintain stable heart function during certain high-risk cardiac procedures, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Zyprexa Relprevv (olanzapine pamoate): Drug Safety Communication - FDA Review of Study Sheds Light on Two Deaths Associated with the Injectable Schizophrenia Drug, FDA MedWatch
• Wegmans Announces Recall of (Frozen) Wegmans Organic Food You Feel Good About Just Picked Spinach, 12 Oz. Which May Be Contaminated With Listeria Monocytogenes, U.S. Food & Drug Administration (FDA)
• Amy's Kitchen Recalls Various Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FSMA Public Meeting, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FSMA Public Meeting, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CFSAN Constituent Update - FSMA Public Meeting, U.S. Food & Drug Administration (FDA)
  • CFSAN Constituent Update - FSMA Public Meeting, U.S. Food & Drug Administration (FDA)
• Taylor Farms Florida Issues Allergen Alert on Undeclared Soy in Kale and Quinoa Salad, U.S. Food & Drug Administration (FDA)
• Giant Eagle Voluntarily Recalls Raisin Filled and Apricot Filled Cookies Due to an Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• Texas Star Nut and Food Co. Inc. Natural Macadamia Nuts Are Being Voluntarily Recalled Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Aurora Products, Inc. Voluntarily Recalls Certain Aurora Natural Brand and Certain Private Label Brand Walnuts and Trail Mixes Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• La Terra Fina Recalls Organic Spinach Dip Sold in Bay Area Costco Clubs, U.S. Food & Drug Administration (FDA)
• Voluntary Recall for Potential Health Risk O’Coconut ™, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Important safety information: Harvoni , and Sovaldi, U.S. Food & Drug Administration (FDA)
• Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
• Infórmese sobre la prevención del VIH en las mujeres, GobiernoUSA.gov
• Cómo proteger su hogar de animales salvajes, GobiernoUSA.gov
• Giant Eagle Voluntary Recall of Bakery Seasonal Cut-Out Shapes Cookies Due to Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Over-the-Counter Asthma Products Labeled as Homeopathic: FDA Statement - Consumer Warning About Potential Health Risks, FDA MedWatch
• Update of CVM's What's New - Draft Agenda for Public Meeting Available, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Draft Guidance to Ensure the Safety of Animal Feed On-Farm, U.S. Food & Drug Administration (FDA)
• Natural Grocers by Vitamin Cottage Expands Recall on Organic Garlic Powder Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• First Source LLC Recalls Wegmans Organic Food You Feel Good About Walnut Halves & Pieces 6oz tubs Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Natural Grocers expands recall on Organic Garlic Powder due to possible health risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 18, 2015, U.S. Food & Drug Administration (FDA)
• Kraft Foods Group Voluntarily Recalls Select Code Dates and Manufacturing Codes of Kraft Macaroni & Cheese Boxed Dinners Due to Possible Metal Pieces, U.S. Food & Drug Administration (FDA)
• Dietary Supplements & Food Labeling Newsletter, U.S. Food & Drug Administration (FDA)
• Product Removal/Foodborne Illness Outbreak Investigation Advisory, U.S. Food & Drug Administration (FDA)
• FDA approves Cholbam to treat rare bile acid synthesis disorders, U.S. Food & Drug Administration (FDA)
• Lo que debe saber para viajar en avión, GobiernoUSA.gov
• Trader Joe’s Recalls Raw Walnuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA to Hold Public Meeting on Alternative In Vitro Bioequivalence Pathways, U.S. Food & Drug Administration (FDA)
• Frontier Co-op Initiates Voluntary Class 1 Recall Due to Possible Health Risk from Organic Garlic Powder, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Primal Pet Foods Voluntarily Recalls A Single Lot of Raw Frozen Cat Food, U.S. Food & Drug Administration (FDA)
• Prepárese ante un desastre natural con el PrepareAthon de América 2015, GobiernoUSA.gov
• Primal Pet Foods Voluntarily Recalls A Single Lot of Raw Frozen Cat Food, U.S. Food & Drug Administration (FDA)
• Trader Joe’s Issues Product Recall & Allergy Alert on Undeclared Peanuts in Cinnamon Almonds, U.S. Food & Drug Administration (FDA)
• Badia Spices, Inc. Issues Allergy Alert on Ground Cumin Products for Undeclared Peaunt Protein, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update, U.S. Food & Drug Administration (FDA)
• March eUpdate from FDA Office of Women's Health, FDA Office of Women's Health
• Giant Eagle Voluntary Recall of Irish Soda Bread Due to Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lactated Ringer's Irrigation, 3000mL by Hospira: Recall - Mold Contamination, FDA MedWatch
• Update of CVM's What's New - Updated Medicated Feed Mill Licenses/Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
• Hospira Issues a Voluntary Nationwide Recall of One Lot of Lactated Ringer's Irrigation Due to Mold Contamination, U.S. Food & Drug Administration (FDA)
• T. Up Trading, Inc. Issues Allergy Alert on Undeclared Milk in Corn Bba, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 11, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - February 2015 Safety Labeling Changes posting includes 45 products with changes to Prescribing Information, FDA MedWatch
• CVM Updates - Federal Judge enters Consent Decree against Specialty Compounding LLC, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Treanda (bendamustine hydrochloride) Solution by Teva: FDA Statement - Not Compatible with Closed System Transfer Devices, Adapters, and Syringes Containing Polycarbonate or Acrylonitrile-Butadiene-Styrene, FDA MedWatch
• Ultra ZX LABS, L.L.C. Issues Voluntary Nationwide Recall of Ultra ZX Since It Contains Undeclared Sibutramine and Phenolphthalein, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Ultra ZX LABS, L.L.C. Issues Voluntary Nationwide Recall of Ultra ZX Since It Contains Undeclared Sibutramine and Phenolphthalein, U.S. Food & Drug Administration (FDA)
• National Women and Girls HIV/AIDS Awareness Day, FDA Office of Women's Health
• Update of CVM's What's New - Public Master Files Updated, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Chantix (varenicline): Drug Safety Communication - FDA Updates Label to Include Potential Alcohol Interaction, FDA MedWatch
• FDA approves CPR devices that may increase chance of surviving cardiac arrest, U.S. Food & Drug Administration (FDA)
• FDA approves new antifungal drug Cresemba, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Magnesium Sulfate in 5 Percent Dextrose Injection by Hospira: Recall - Incorrect Barcode Labeling, FDA MedWatch
• Hospira Issues a Voluntary Nationwide Recall of One Lot of Magnesium Sulfate in 5% Dextrose Injection Due to Incorrect Barcode Labeling, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Plum A+ and Plum A+3 Infusion Systems by Hospira: Class I Recall - Alarm Volume Failure, FDA MedWatch
• FDA authorizes use of first device to treat patients with dialysis-related amyloidosis, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Hospira Plum A+ and Plum A+3 Infusion Systems - Alarm Volume Failure, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 0.9 Percent Sodium Chloride Injection, USP, 250 mL VisIV Container by Hospira: Recall - Particulate Matter, FDA MedWatch
• CVM Updates - The FDA Issues Final Guidances for Animal Drug Depletion Studies, U.S. Food & Drug Administration (FDA)
• FDA approves first biosimilar product Zarxio, U.S. Food & Drug Administration (FDA)
• Hospira Issues A Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection, USP, 250 mL VisIV Container Due to Particulate Matter, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 04, 2015, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA’s Survey of Milk Finds Few Drug Residues, U.S. Food & Drug Administration (FDA)
• Evite multas tributarias por no tener seguro médico, GobiernoUSA.gov
• FDA launches drug shortages mobile app, U.S. Food & Drug Administration (FDA)
• FDA expands approved use of Opdivo to treat lung cancer, U.S. Food & Drug Administration (FDA)
• Siete pasos para mantener su número de teléfono al cambiar de proveedor, GobiernoUSA.gov
• Maternal Science, Inc. Issues Allergy Alert on Undeclared Milk in healthy mama® Boost It Up!tm Mango Drink, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Global Animal Health Conference, U.S. Food & Drug Administration (FDA)
• Comparta el transporte a la escuela, GobiernoUSA.gov
• FDA MedWatch - Testosterone Products: Drug Safety Communication - FDA Cautions About Using Testosterone Products for Low Testosterone Due to Aging; Requires Labeling Change to Inform of Possible Increased Risk of Heart Attack And Stroke, FDA MedWatch
• Update of CVM's What's New - Animal Drug Approvals March 2015 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Ateeco, Inc., Maker of Mrs. T’s Pierogies, Issues Voluntary Regional Product Recall of Mozzarella, Tomato & Basil Pierogies Due to Plastic Contamination, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: HeartWare Ventricular Assist System (VAS) – Electrostatic Discharge May Cause Pump Failure, U.S. Food & Drug Administration (FDA)
• REGISTER NOW: Patient-Focused Drug Development, FDA Office of Women's Health
• FDA MedWatch - HeartWare Ventricular Assist System Controllers: Recall - Clinical Trial Controllers Susceptible to Electrostatic Discharge, FDA MedWatch
• Heartware International Recalls Certain Older Heartware Clinical Trial Controllers, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Releases Biannual Progress Report on Judicious Use of Antimicrobials in Food-producing Animals, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 25, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - MAQUET Servo Humidifier 163 by Teleflex Medical: Class I Recall - Cracks in Connector Tubes May Lead to Leak Failures, FDA MedWatch
• FDA approves new antibacterial drug Avycaz, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Teleflex Medical, MAQUET Servo Humidifier 163 - Connector Cracks and Cracks in Connector Tubes, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Colistimethate for Injection USP, 150 mg and Rifampin for Injection USP, 600 mg/vial by Heritage Pharmaceuticals: Recall - Lack of Sterility Assurance, FDA MedWatch
• Heritage Pharmaceuticals Initiates a Nationwide Voluntary Recall of Colistimethate for Injection USP, 150 mg and Rifampin for Injection USP, 600 mg/vial Due to a Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Magnetic Resonance Imaging (MRI) Systems with Magnet Rundown Unit by GE Healthcare: Class I Recall - Potential Diabling of the Magnet Rundown Unit, FDA MedWatch
• Temporada de impuestos sin estrés, GobiernoUSA.gov
• Update of CVM's What's New - FSMA Update - Save the Date, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: GE Healthcare Magnetic Resonance Imaging (MRI) Systems with Magnet Rundown Unit, U.S. Food & Drug Administration (FDA)
• Fairway “Like No Other Market” Recalls Fairway Brand Raw Hazelnuts (Filberts) Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Atracurium Besylate Injection by Sagent Pharmaceuticals: Recall - Potential Impact on Product Sterility, FDA MedWatch
• Update of CVM's What's New - Purina Animal Nutrition LLC Recalls One Lot of DuMOR® Sheep Formula, 50 lbs. Bags Due to Potentially High Level of Copper, U.S. Food & Drug Administration (FDA)
• Purina Animal Nutrition LLC Recalls One Lot of DuMOR Sheep Formula, 50 lbs. Bags Due to Potentially High Level of Copper; Distributed only in Florida, U.S. Food & Drug Administration (FDA)
• Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of Atracurium Besylate Injection, USP, 50mg/5mL and 100mg/10mL due to FDA Observations Pertaining toAseptic and GMP Practices at the Manufacturer’s Site Potentially Impacting Product Sterility, U.S. Food & Drug Administration (FDA)
• FDA approves Farydak for treatment of multiple myeloma, U.S. Food & Drug Administration (FDA)
• CVM Updates - The FDA Issues Draft Guidance to Help Evaluate Effectiveness of Drugs to Reduce Pathogenic Shiga Toxin-Producing E. coli in Cattle, U.S. Food & Drug Administration (FDA)
• Hummingbird Wholesale Issues Allergy Alert on Undeclared Milk in Organic Chocolate Hazelnut Butter, U.S. Food & Drug Administration (FDA)
• CON YEAGER SPICE COMPANY'S REVISED VOLUNTARY RECALL FOR GROUND CUMIN AND SEASONING BLENDS (CONTAINING GROUND CUMIN)DUE TO POTENTIAL UNDECLARED PEANUT ALLERGENS, U.S. Food & Drug Administration (FDA)
• WhiteWave Foods Voluntarily Recalls Horizon Cheddar Sandwich Crackers, U.S. Food & Drug Administration (FDA)
• Old Home Kitchens Issues Allergy Alert and Voluntary Recall on Undeclared Pecans In "Sock It To Me Creme Cake", U.S. Food & Drug Administration (FDA)
• Urgent: El Popocatepetl Ind., Inc. issues an allergy alert on Undeclared Milk and Yellow #5 in 8 in. Sundried Tomato, Spinach Pesto, and Chipotle Wraps, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 18, 2015, U.S. Food & Drug Administration (FDA)
• FDA approves closure system to permanently treat varicose veins, U.S. Food & Drug Administration (FDA)
• New Blog: Recent Progress on Demographic Information and Clinical Trials, FDA Office of Women's Health
• Chilean Mushrooms is recalling its Chilean Mushrooms because they contained undeclared sulfites, U.S. Food & Drug Administration (FDA)
• Chocolate By Design Inc. Issues Allergy Alert on Undeclared Egg in Milk Chocolate Assorted Character Icing Pops, Christmas Icing Pops and Triple Heart Icing Pops, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Endoscopic Retrograde Cholangiopancreatography (ERCP) Duodenoscopes: FDA Safety Communication - Design May Impede Effective Cleaning, FDA MedWatch
  • <Possible follow-ups>
  • FDA MedWatch - Endoscopic Retrograde Cholangiopancreatography (ERCP) Duodenoscopes: FDA Safety Communication - Design May Impede Effective Cleaning, FDA MedWatch
• CVM Updates - FDA Issues Update on Jerky Pet Treat Investigation, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Design of Endoscopic Retrograde Cholangiopancreatography (ERCP) Duodenoscopes May Impede Effective Cleaning: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Spiceco Issues A Correction Regarding Allergy Alert On Undeclared Peanut Allergen In 5 Oz. Containers Of Pride Of Szeged Sweet Hungarian Paprika Lot #091617PAHU05PS and Lot #091717PAHU05PS, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Isentress (raltegravir) label update, U.S. Food & Drug Administration (FDA)
• Lo que usted debe saber para convertirse en ciudadano estadounidense, GobiernoUSA.gov
• Goya Foods, Inc. Announces Recall of Kirby Brand Black Beans with Creole Seasoning and Goya Brand Black Bean Soup for Undeclared Peanut Protein, U.S. Food & Drug Administration (FDA)
• Mitos y realidades sobre los impuestos, GobiernoUSA.gov
  • <Possible follow-ups>
  • Mitos y realidades sobre los impuestos, GobiernoUSA.gov
• FDA Classifies Previous Covidien Field Action For Its Trellis-6 and Trellis-8 Peripheral Infusion Systems as a Class 1 Recall, U.S. Food & Drug Administration (FDA)
• Press Release for Hanbit Enterprises, Inc. dba Jack and the Beanstalk Recalls Soybean Sprouts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• T. Marzetti Co Issues Allergy Alert on Undeclared Milk and Egg in Single Serve Packets of Larosa’s Creamy Garlic Dressing Due to Label Issue, U.S. Food & Drug Administration (FDA)
• Whole Foods Market’s Glastonbury Store Recalls Divine Treasures 100,000 Smooches Vegan Chocolate Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• Whole Foods Market’s Southwest Region Recalls Chocolate Cake For Two Due To Undeclared Egg, U.S. Food & Drug Administration (FDA)
• Moscahlades Bros Inc. Recalls Hellas Golden Double Smoked Herring Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Lenvima for a type of thyroid cancer, U.S. Food & Drug Administration (FDA)
• Natural Grocers by Vitamin Cottage Issues Recall on Organic Garlic Powder Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 11, 2015, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses/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/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/Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
• New data shows test can help physicians remove patients with suspected TB from isolation earlier, U.S. Food & Drug Administration (FDA)
• FDA permits marketing of fecal incontinence device for women, U.S. Food & Drug Administration (FDA)
• Kent, WA Firm Issues Allergy Alert on Undeclared Soy and Egg Allergens in Small Heart Strawberry Tray with Devonshire Dip, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Notice of Public Meetings, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Pet Food Recalls, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Pet Food Recalls, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Pet Food Recalls, U.S. Food & Drug Administration (FDA)
• Sunfood Voluntarily Recalls Organic Sacha Inchi Powder Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Pet International Inc. Recalls 6” Beef Trachea Pet Treat Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Tuffy's Pet Foods, Inc. Issues Voluntary Recall of a Limited Quantity of Nutrisca Dry Dog Food Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medicina alternativa para síntomas comunes, GobiernoUSA.gov
• FDA MedWatch - Ketorolac Tromethamine Injection by Hospira: Recall - Particulate in Glass Vials, FDA MedWatch
• BLOG: The Meaning of Wearing Red, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Trellis 6 and Trellis 8 Peripheral Infusion Systems by Covidien: Class I Recall - Balloon Inflation Ports Mislabeled, FDA MedWatch
• Hospira Issues a Voluntary Global Recall of Multiple Lots of Ketorolac Tromethamine Injection Due to Potential Particulate in Glass Vials, U.S. Food & Drug Administration (FDA)
• Solo quedan 4 días para inscribirse en un plan de seguro médico, GobiernoUSA.gov
• Medical Device Safety and Recalls: Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems Labeling Issue, U.S. Food & Drug Administration (FDA)
• Spiceco Extends an Allergy Alert on Undeclared Peanut Allergen in 5 oz. Containers of Pride of Szeged Sweet Hungarian Paprika Lot # 091717PAHU05PS, U.S. Food & Drug Administration (FDA)
• Hines Nut Company, Dallas, TX Announces Voluntary Recall of Walnut Halves and Pieces Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Pepperidge Farm Issues Voluntary Recall of Bagels in Select States Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• National Choice Bakery Issues Allergy Alert on Undeclared Peanuts & Tree Nuts in Bagels, U.S. Food & Drug Administration (FDA)
• Updated Press Release for Korean Food Co. Recalls Soybean Sprout Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Items Prepared With Supplier-provided Ground Cumin Spice Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Dutrebis approved, though not commercially marketed in US at this time, U.S. Food & Drug Administration (FDA)
• Detox Transforms Health and Nutrition Issues Voluntary Nationwide Recall of Dietary Supplements Due to the Presence of Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• FDA clears system to reduce stroke risk during stent and angioplasty procedures, U.S. Food & Drug Administration (FDA)
• Bimbo Bakeries USA Issues Allergy Alert and Voluntary Regional Recall of Thomas’, Sara Lee and Jewel Bagels Sold in Select Midwest States, U.S. Food & Drug Administration (FDA)
• Korean Food Co. Recalls Soybean Sprout Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• See’s Candies, Inc. Issues Allergy Alert on Undeclared Nuts in 8 Oz Classic Red Heart with Assorted Chocolates, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - J.J. Fuds, Inc. Expands Recall of Pet Food Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• J.J. Fuds, Inc. Expands Recall of Pet Food Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• February e-Update from the FDA Office of Women's Health, U.S. Food & Drug Administration (FDA)
• Middle East Bakery, Inc. Expands Allergy Alert Due to the Potential for Undeclared Soy in Select Lots of Joseph’s Bread Products and Trader Joe's Pita Products, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals February 2015 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Christ Kitchen Issues Allergy Alert on Undeclared Milk in Blameless Blondies Cookie Bar, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Commissioner Margaret A. Hamburg Stepping Down, U.S. Food & Drug Administration (FDA)
• The February 2015 MedSun Newsletter is now, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 04, 2015, U.S. Food & Drug Administration (FDA)
• The Jefferson Street Bakery Issues Allergy Alert On Undeclared Milk In "Amana Dinner Rolls", U.S. Food & Drug Administration (FDA)
• Lo que usted debe saber sobre el sarampión, GobiernoUSA.gov
• Wyked Labs Issues Voluntary Nationwide Recall of Eight Dietary Supplement Products Due to Presence of Prohormone Ingredients, U.S. Food & Drug Administration (FDA)
• FDA approves first tissue adhesive for internal use, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Raw Macadamia Nuts from Stores in AL, GA, MS, NC, SC and TN Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Ibrance for postmenopausal women with advanced breast cancer, U.S. Food & Drug Administration (FDA)
• Conozca el Sistema Nacional de Personas Desaparecidas y No Identificadas, GobiernoUSA.gov
• The Spice Mill issues Allergy Alert on Undeclared Peanut Protein in Ground Cumin and Cajun Seasoning Products, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FSMA and Animal Feed Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - FSMA and Animal Feed Update, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - FSMA and Animal Feed Update, U.S. Food & Drug Administration (FDA)
• Middle East Bakery, Inc. Issues Allergy Alert due to the potential for Undeclared Soy in select lots of Joseph’s Bread Products and Trader Joe's Pita Products, U.S. Food & Drug Administration (FDA)
• FDA seeks $4.9 billion for FY 2016 to implement the FDA Food Safety Modernization Act and improve the quality and safety of the medical products Americans use, U.S. Food & Drug Administration (FDA)
• Sole Grano LLC Issues Allergy Alert on Undeclared Almonds & Wheat in, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - February 2015, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Grill-Phoria LLC Recalls Big Bark All Natural Beef Jerky Treats for Dogs Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Hamchorom, Inc. Issues Allergy Alert On Undeclared Milk and Egg In HAITAI Tayo and HAITAI Gyeran Crackers, U.S. Food & Drug Administration (FDA)
• Aloha Voluntarily Recalls Line Of Premium Protein Products Due To A Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Grill-Phoria LLC Recalls Big Bark All Natural Beef Jerky Treats for Dogs Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Flowers Foods Issues Allergy Alert and Voluntary Recall on Market Basket Original English Muffins Sold in Massachusetts, Maine, and New Hampshire, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 28, 2015, U.S. Food & Drug Administration (FDA)
• Serie completa de monedas presidenciales para 2015, GobiernoUSA.gov
• FDA expands uses of Vyvanse to treat binge-eating disorder, U.S. Food & Drug Administration (FDA)
• United States enters consent decree prohibiting illegal distribution of Luvena Prebiotic products, U.S. Food & Drug Administration (FDA)
• Spiceco Issues Allergy Alert on Undeclared Peanut Allergen in 5 Oz. Containers of Pride of Szeged Sweet Hungarian Paprika Lot # 091617PAHU05PS, U.S. Food & Drug Administration (FDA)
• Georgia Company Recalls Certain Pecan Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Guidances Under Development for 2015, U.S. Food & Drug Administration (FDA)
• Freeland Foods Voluntarily Recalls Sunflower Seed Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• REO Spice & Seasoning, Inc VoluntarilyRrecalls REO Country Style Chili Seasoning Due to Undeclared Peanut Allergens, U.S. Food & Drug Administration (FDA)
• Aleias Gluten Free Foods, LLC Issues Allergy Alert on Undeclared Peanut Protein in Parmesan Croutons and Classic Croutons, U.S. Food & Drug Administration (FDA)
• Aron Streit, Inc. Issues Allergy Alert On Undeclared Milk Allergens In "Streit's Dark Chocolate Coins", U.S. Food & Drug Administration (FDA)
• Arcadia Tradings Inc. Recalls Red Thread Fish Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Prezcobix tablet containing 800 mg of darunavir and 150 mg of cobicistat approval, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of Evotaz, containing 300 mg of atazanavir and 150 mg of cobicistat, U.S. Food & Drug Administration (FDA)
• Approval changes to the Kaletra (lopinavir/ritonavir), U.S. Food & Drug Administration (FDA)
• FDA takes steps to improve reliability of automated external defibrillators, U.S. Food & Drug Administration (FDA)
• Dairy Recall, U.S. Food & Drug Administration (FDA)
• Probar LLC Recalls Probar Base Frosted Peanut Butter Bars Due to Possible Presence of Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• Lime Green Grocer, Inc. Issues Allergy Alert on Undeclared Soy in the Thai Delight Burrito, U.S. Food & Drug Administration (FDA)
• Infórmese sobre las drogas y el abuso de sustancias entre adolescentes, GobiernoUSA.gov
• Update of CVM's What's New - Cancellation of 2015 Windows to Regulatory Research Internship Program, U.S. Food & Drug Administration (FDA)
• FDA approves first generic esomeprazole, U.S. Food & Drug Administration (FDA)
• Comunicado Actualizado: Quesería Bendita LLC Retira Quesos Frescos Y Crema Agria Debido a Posibles Riesgos Para la Salud, U.S. Food & Drug Administration (FDA)
• Dr. Robert Califf named FDA Deputy Commissioner for Medical Products and Tobacco, U.S. Food & Drug Administration (FDA)
• Korean Food Co. Issues Allergy Alert on Undeclared Shrimp in Mak Kimchi, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Recalls, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Recalls, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Recalls, U.S. Food & Drug Administration (FDA)
• Cox Veterinary Laboratory, Inc. Issues Voluntary Recall of “Gastroade Xtra”, U.S. Food & Drug Administration (FDA)
• J.J. Fuds, Inc. Issues Recall of Pet Food Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Natpara to control low blood calcium levels in patients with hypoparathyroidism, U.S. Food & Drug Administration (FDA)
• FDA approves a second vaccine to prevent serogroup B meningococcal disease, U.S. Food & Drug Administration (FDA)
• FDA permits marketing of first system of mobile medical apps for continuous glucose monitoring, U.S. Food & Drug Administration (FDA)
• Second Turkish man sentenced for smuggling counterfeit cancer drugs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 0.9 Percent Sodium Chloride Injection, USP, 250 mL by Hospira : Recall - Particulate Matter, FDA MedWatch
• Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection, USP, 250 mL Due to Particulate Matter, U.S. Food & Drug Administration (FDA)
• Freeland Foods Voluntarily Recalls Spicy Seed Due To Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Gonnella Baking Company Issues Allergy Alert on Undeclared Milk in Jewel Brand Gourmet Sandwich Rolls and Gonnella Brand Sub Buns, U.S. Food & Drug Administration (FDA)
• Tarrier Foods Issues Allergy Alert on Undeclared Peanuts and Egg in Chopped Twix, U.S. Food & Drug Administration (FDA)
• Reconozca las etiquetas y los códigos de sus alimentos, GobiernoUSA.gov
• FDA MedWatch - Bone Graft Substitutes Containing Recombinant Proteins or Synthetic Peptides in Patients Under Age 18: FDA Safety Communication - Reports of Serious Injuries, FDA MedWatch
• Medical Device Safety and Recalls: Use of Bone Graft Substitutes Containing Recombinant Proteins or Synthetic Peptides in Patients under Age 18 – FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Northern Tier Bakery Issues Allergy Alert on Potential Undeclared Peanut in Product, U.S. Food & Drug Administration (FDA)
• CVM Updates - New FDA Guidance Document Search Now Available, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FSMA and Animal Feed, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - FSMA and Animal Feed, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Oma’s Pride Recalls Purr Complete Feline Poultry Meal because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• B&M, Inc. Issues Allergy Alert on Undeclared Peanut Protein in Ground Seasonings Sold at Harris Teeter in the Southeast Region Due to Potential Undeclared Peanut Protein, U.S. Food & Drug Administration (FDA)
• Oma's Pride Recalls Purr Complete Feline Poultry Meal because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• B&M, Inc. Issues Allergy Allert on Undeclared Peanut Protein in Ground Cumin and Other Seasonings Sold at Target and the Fresh Market Nationwide due to Potential Undeclared Peanut Protein, U.S. Food & Drug Administration (FDA)
• Inventure Foods, Inc. Issues Voluntary Recall Of Its Rader Farms Fresh Start Smoothie Blend, Sunrise Refresh Fusion, And Daily Power Fusion Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Queseria Bendita LLC Recalls Fresh Cheeses and Sour Cream Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 14, 2015, U.S. Food & Drug Administration (FDA)
• Haga crecer su negocio con el Programa de Desarrollo Empresarial 8(a), GobiernoUSA.gov
• Food Safety Recalls & Alerts, FoodSafety.gov
  • <Possible follow-ups>
  • Food Safety Recalls & Alerts, FoodSafety.gov
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  • Food Safety Recalls & Alerts, FoodSafety.gov
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  • Food Safety Recalls & Alerts, FoodSafety.gov
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