FDA News Releases

• Date Index

• P&G Expands Voluntary Limited Recall of Specialized Dry Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• KCB Issues Allergy Alert on Possible Eggs In "KCB No Eggs Added Cake Rusk 28oz", U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Allergy Alert: Eggs in "Cake Rusk", FoodSafety.gov
• Nimodipine Oral Capsules: Medication Errors - IV Administration May Result in Death, Serious Harms, FDA MedWatch
• FDA MedWatch - NeoProfen (ibuprofen lysine) Injection: Recall and Shortage - Risk of Particulate Matter, FDA MedWatch
• STATEMENT BY MARGARET A. HAMBURG, COMMISSIONER OF FOOD AND DRUGS ON THE REOPENING OF SOME MISSISSIPPI STATE WATERS TO COMMERCIAL FISHING, U.S. Food & Drug Administration (FDA)
• STATEMENT BY MARGARET A. HAMBURG, COMMISSIONER OF FOOD AND DRUGS ON THE REOPENING OF FLORIDA STATE WATERS TO COMMERCIAL FISHING, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Draft Compliance Policy Guide: Salmonella in Animal Feed, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces FY 2011 Animal Drug/Animal Generic Drug User Fees, U.S. Food & Drug Administration (FDA)
• United States Seeks Permanent Injunction Against New York Food Processor, U.S. Food & Drug Administration (FDA)
• Lundbeck Inc. Announces the Voluntary Nationwide Recall of Two Lots of NeoProfen® (ibuprofen lysine) Injection Recall will Result in Temporary Product Shortage, U.S. Food & Drug Administration (FDA)
• Bay Valley Foods Issues Allergy Alert on Undeclared Egg and Wheat in Cans of Mislabeled Chef's Cupboard Chicken with Rice Soup, U.S. Food & Drug Administration (FDA)
• FDA Approves Vaccines for the 2010-2011 Influenza Season, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Approves Vaccines for the 2010-2011 Influenza Season, U.S. Dept. of Health & Human Services
• FDA Warns Consumers of Serious Harm from Drinking Miracle Mineral Solution (MMS), U.S. Food & Drug Administration (FDA)
• Join us Today at 1:00pm ED for a Special HealthCare.gov Webchat, HealthCare.gov
• FDA MedWatch - Miracle Mineral Solution (MMS): Product as consumed produces a potent bleach that can cause serious harm, FDA MedWatch
• FDA MedWatch - Afluria (CSL Ltd.) Influenza Virus Vaccine: Label Change - Risk of Fever and Febrile Seizure, FDA MedWatch
• FDA MedWatch - Nutraloid Labs ejaculoid XXTREME and stimuloid II: Undeclared Drug Ingredient, FDA MedWatch
• Prevention and Control of Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices (ACIP), 2010, U.S. Dept. of Health & Human Services
• NIAID Grantees Use New Skin Patches to Deliver Flu Vaccine in Mice, U.S. Dept. of Health & Human Services
• The August 2010 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Evamist Hormone Spray May Cause Illness in Pets, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Pennsylvania Dairy Farm Agrees to Stop Improper Medication, U.S. Food & Drug Administration (FDA)
• FDA Statement on the Reopening of Some La. State Waters to Commercial Fishing, U.S. Food & Drug Administration (FDA)
• Today: Don Berwick highlights Medicare's 45th Anniversary, HealthCare.gov
• FoodSafety.gov Recall: Organic Alfalfa Sprouts, FoodSafety.gov
• Specialty Farms, LLC Expands Recall of Organic Alfalfa Sprouts Blend and Organic Sprout Salad in the North Eastern United States Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Nutraloid Labs Inc. Conducts Voluntary Nationwide Recall of Two Dietary Supplements Found to Contain Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Evamist (estradiol transdermal spray): Drug Safety Communication - Unintended Exposure of Children and Pets to Topical Estrogen, FDA MedWatch
• FDA Advisory: Avoid Unintentional Exposure of Children and Pets to Evamist, U.S. Food & Drug Administration (FDA)
• Former CEO of Seafood Importing Corporation Sentenced to Federal Prison for Importing Falsely Labeled Fish, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cubicin (daptomycin): Drug Safety Communication - Risk of Eosinophilic Pneumonia, FDA MedWatch
• Enforcement Report for July 28, 2010, U.S. Food & Drug Administration (FDA)
• FDA Approves Drug for Chronic Drooling in Children, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Mice Direct Recalls Frozen Reptile Feed Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• New Early Detection System Helps FDA Identify More than 100 Food Safety Problems in First 7 Months, U.S. Food & Drug Administration (FDA)
• Biggers & Callaham, Llc Dba Mice Direct Recalls Frozen Reptile Feed Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Voluntary Recall of PreserVision® Eye Vitamin AREDS 2 Formula in the United States, U.S. Food & Drug Administration (FDA)
• Federal Agents Seize FastSize Extenders and FastSize EQM Erectile Quality Monitors, U.S. Food & Drug Administration (FDA)
• P&G Recalls Two Lots of Prescription Renal Diet Cat Food due to a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Pennsylvania Dairy Farm Agrees to Stop Improper Medication, U.S. Food & Drug Administration (FDA)
• Airgas South Initiates Precautionary Voluntary Recall of Medical Gas Products at Chattanooga, TN Facility, U.S. Food & Drug Administration (FDA)
• Foodsafety.gov Recall: Corn/Pepper Blend (Chipotle Mexican Grill Restaurant), U.S. Dept. of Health & Human Services
• Oregon Ice Cream Company Issues Allergy Alert on Undeclared Peanuts in Denali Bear Claw Ice Cream, U.S. Food & Drug Administration (FDA)
• Specialty Farms, LLC Recalls Organic Alfalfa Sprouts Blend and Organic Sprout Salad in the North Eastern United States Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Pasco Processing LLC, Announces Voluntary Product Recall Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Approves First Generic Enoxaparin Sodium Injection, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov ALLERGY ALERT: Corn Pasta, U.S. Dept. of Health & Human Services
• FDA Approves First Generic Enoxaparin Sodium Injection to Prevent DVT, U.S. Food & Drug Administration (FDA)
• Cook brand Ciaglia Blue Rhino/Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets/Trays:Recall due to balloon inflation assembly that may not hold air, FDA MedWatch
• Joyful Slim Herb Supplement:Recall-Undeclared Drug Ingredient:Sibutramine and risk of inintended cardiovascular effects, FDA MedWatch
• DeBoles^® Nutritional Foods, Inc. Voluntarily Recalls One Lot Code of DeBoles^®Kids Only! Gluten Free Tubettini Corn Pasta Due to the Presence of an Undeclared Allergen, Lot Code 30JUN11D1, U.S. Food & Drug Administration (FDA)
• Federal Government Seizes Cyanide Antidote Kits from California Company, U.S. Food & Drug Administration (FDA)
• J & H Besta Corp. Issues a Voluntary Nationwide Recall of Joyful Slim Herb Supplement Found to Contain an Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 21, 2010, U.S. Food & Drug Administration (FDA)
• Webchat on Health Reform with Secretary Sebelius, MomsRising and Fran Drescher, HealthCare.gov
• Cook Initiates Voluntary Recall of Certain Ciaglia Blue Rhino and Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets and Trays that Contain a Covidien 6PERC or 8PERC Shiley[TM] Tracheostomy Tube, U.S. Food & Drug Administration (FDA)
• CONSTELLATION Vision System: Recall, FDA MedWatch
• New Diabetes Publications for Women, U.S. Food & Drug Administration (FDA)
• Vialipro Dietary Supplement: Recall-Undeclared Drug Ingredient, FDA MedWatch
• Foodsafety.gov - Recalls: Chicken Nuggets, Herring, U.S. Dept. of Health & Human Services
• Good Health, Inc. Issues a Nationwide Voluntary Recall of Product Marketed as Dietary Supplement, U.S. Food & Drug Administration (FDA)
• NIH Scientists Advance Universal Flu Vaccine, U.S. Dept. of Health & Human Services
• FDA and Other Federal Agencies Collaborate to Improve Chemical Screening, U.S. Food & Drug Administration (FDA)
• New Jersey Woman Sentenced for Committing Insurance Fraud and Selling Prescription Fertility Drugs via the Internet, U.S. Food & Drug Administration (FDA)
• Slim-30 Herb Supplement: Undeclared Drug Ingredient, FDA MedWatch
• D & M Smoked Fish, Inc. Issues an Allert on Uneviscerated Schmaltz Herring, U.S. Food & Drug Administration (FDA)
• J & H Besta Corp. Issues a Voluntary Nationwide Recall of Slim- 30 Herb Supplement Found to Contain an Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Advair Diskus (fluticasone propionate and salmeterol inhalation powder): Stolen Product Warning, FDA MedWatch
• Update of CVM's What's New - The Journey of an Animal Drug through the Approval Process, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov - RECALL: Raw Cat Food, U.S. Dept. of Health & Human Services
• Feline's Pride Expands Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Feline's Pride Expands Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Angiotensin Receptor Blockers (ARBs): Ongoing Safety Review for Cancer Risk, FDA MedWatch
• June 2010 Drug Safety Labeling Changes: 28 Medical Product Labels with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• Fresh Express Announces Recall of Expired Romaine Lettuce Products with Use-By Dates of July 8 to 12 and "S" in the Product Code Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recall: Fresh Express Romaine Lettuce Products, U.S. Dept. of Health & Human Services
• Diamond Usa Inc. Issues Allergy Alert On Undeclared Sulfites In "Dry Apricot Rolled", U.S. Food & Drug Administration (FDA)
• ALLERGY ALERTS: Broccoli Raisin Salad, Apricots, U.S. Dept. of Health & Human Services
• Conference call on preventive care in the Affordable Care Act and Women and Prevention, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 14, 2010, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Coumadin 1 mg Tablet Blister Packs: Recall, FDA MedWatch
• Bristol-Myers Squibb Initiates a Nationwide Voluntary Recall of Coumadin (R) 1 mg Tablet Blister Packs, U.S. Food & Drug Administration (FDA)
• Arava (leflunomide): Boxed Warning- Risk of Severe Liver Injury, FDA MedWatch
• FDA Issues Requirements for Baxter Healthcare Infusion Pump Recall, U.S. Food & Drug Administration (FDA)
• Recalls: Sliced Apples, Protein Powder, U.S. Dept. of Health & Human Services
• Florida Company Recalls Sliced Apples, U.S. Food & Drug Administration (FDA)
• Spanish: Federal Agents Seize Bee-Shield Hand Sanitizer from Puerto Rican Company, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Air- or Gas-Pressurized Spray Devices: Risk of Air or Gas Embolism, FDA MedWatch
• Federal Agents Seize Bee-Shield Hand Sanitizer from Puerto Rican Company, U.S. Food & Drug Administration (FDA)
• RECALLS: Chile Peppers, Frozen Avocado Pulp, U.S. Dept. of Health & Human Services
• FDA: New Final Rule to Ensure Egg Safety, Reduce Salmonella Illnesses Goes Into Effect, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update -Tentative approval of fixed dose combination lamivudine, nevirapine, and zidovudine tablets for Oral Solution, 30 mg/50 mg/60 mg), U.S. Food & Drug Administration (FDA)
• FDA Basic Video: Lawrence Deyton Discusses Tobacco (Video), U.S. Food & Drug Administration (FDA)
• McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products in the United States, Fiji, Guatemala, Dominican Republic, Puerto Rico, Trinidad & Tobago, and Jamaica, U.S. Food & Drug Administration (FDA)
• Miravalle Foods Inc. Recalls Chile California & Chile Nuevo Mexico Peppers Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• J. Hellman Frozen Foods, Inc. Recalls Señor Mexicano[TM] Avocado Pulp Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Qualaquin (quinine sulfate): New Risk Management Plan due to potential for serious hematological reactions, FDA MedWatch
• FDA MedWatch - Que She Herbal Supplement: Undeclared drug ingredients could interact with other medications, FDA MedWatch
• Update of CVM's What's New - July 2010 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• FDA Public Health Alert: Que She Weight Loss Capsules Contain Potentially Harmful Ingredients, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Minor Use/Minor Species Grant Program Request for Applications, U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers, Pharmacists, and Wholesalers Not to Use Stolen Advair Diskus Inhalers, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Warns Consumers, Pharmacists, and Wholesalers Not to Use Stolen Advair Diskus Inhalers, U.S. Food & Drug Administration (FDA)
• FDA Warns of Risks with Unapproved Use of Malaria Drug Qualaquin, U.S. Food & Drug Administration (FDA)
• Ready Pac Foods, Inc. Announces Voluntary Product Recall because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Ready Pac Foods, Inc. Announces Voluntary Product Recall Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• What does 'recall' mean?, U.S. Food & Drug Administration (FDA)
• What products are regulated as electronic products that emit radiation?, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 7, 2010, U.S. Food & Drug Administration (FDA)
• FDA Seeks Public Comment on New Federal Menu Labeling Requirements, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Infergen (interferon alfacon-1) label revision: combination therapy, weight-based dosing, and label format, U.S. Food & Drug Administration (FDA)
• Webinar on FDA's Safety Monitoring of Approved Vaccines, U.S. Food & Drug Administration (FDA)
• Recall: Dog Treats (Possible Salmonella), U.S. Dept. of Health & Human Services
• FDA MedWatch - July 2010 FDA Patient Safety News now available, FDA MedWatch
• The July 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Merrick Pet Care Recalls Beef Filet Squares 10oz Bag (Item #60016 Lot # 10084TL7 Best By March 24, 2012) Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Aquaculture Brochure, U.S. Food & Drug Administration (FDA)
• Merrick Pet Care Recalls Beef Filet Squares 10oz Bag (Item #60016 Lot # 10084TL7 Best By March 24, 2012) Because Of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Approves First Implantable Miniature Telescope to Improve Sight of AMD patients, U.S. Food & Drug Administration (FDA)
• Recalls: Bison/Buffalo Products, Vitamins for Dogs, Energy Mix, U.S. Dept. of Health & Human Services
• Update of CVM's What's New - United Pet Group Voluntarily Expands Recall of Nutritional Supplements For Dogs to Include Additional Tablet and Powdered-Form Products for Dogs and Cats Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Undeclared Peanuts and Chocolate Flavored Chips in Select Containers of Fairway "Energy Mix" and Setton Farms "Total Energy Mix", U.S. Food & Drug Administration (FDA)
• United Pet Group Voluntarily Expands Recall of Nutritional Supplements For Dogs to Include Additional Tablet and Powdered-Form Products for Dogs and Cats Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Pharmacy Owner Sentenced to Over 4 Years for Health Care Fraud, Aggravated Identity Theft and Conspiracy to Misbrand Drugs, U.S. Food & Drug Administration (FDA)
• Is FDA responsible for regulating pesticides that are used in animal products?, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cepheid Xpert MRSA/SA Blood Culture Assay for Use with the GeneXpert Dx System: Class I Recall, FDA MedWatch
• FDA MedWatch - LIFEPAK 20 and LIFEPAK 20e External Defibrillator/Monitors by Physio-Control Inc.: Class I Recall Due To Power Supply Failure, FDA MedWatch
• Get Food Recalls & Allergy Alerts on Your Smart Phone, U.S. Dept. of Health & Human Services
• Cheese Recall and Allergy Alerts (Gelato, Custard Pie, Sausage), U.S. Dept. of Health & Human Services
• Azteca Linda Corp. Recalls QUESO FRESCO and QUESO HEBRA Because of Possible Risk of Health, U.S. Food & Drug Administration (FDA)
• DOMEGA NY INTERNATIONAL CO., LTD Issues Allergy Alert on Undeclared Milk Powder in FUMA CUSTARD PIE, U.S. Food & Drug Administration (FDA)
• I Dolce Inc. Issues Allergy Alert on Undeclared Peanuts in "Gelato", U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Feline's Pride Issues Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Feline's Pride Issues Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Feline's Pride Issues Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination, U.S. Dept. of Health & Human Services
• RECALL: Chicken of the Sea Solid White Tuna in Water, U.S. Dept. of Health & Human Services
• Tri-Union Seafoods Issues Precautionary, Voluntary Recall of Limited 12-Ounce Solid White Tuna in Water, U.S. Food & Drug Administration (FDA)
• The July 2010 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 30, 2010, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • HIV/AIDS Update, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Storing, Handling and Using Animal Milk Replacer Products, U.S. Food & Drug Administration (FDA)
• NOAA, FDA, and Gulf Coast State Officials Affirm Commitment to Ensuring Safety of Gulf Coast Seafood, U.S. Food & Drug Administration (FDA)
• FDA Approves First Generic Effexor Extended Release Capsules to Treat Major Depressive Disorder, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated MUMS Designation List and June 2010 Green Book Update, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Guidance for Industry and FDA: Advisory Levels for Deoxynivalenol (DON) in Grains and Grain By-Products used for Animal Feed, U.S. Food & Drug Administration (FDA)
• INZ Distributors Inc./Magic Power Coffee Inc. Conducts a Voluntary Nationwide Recall of Magic Power Coffee Dietary Supplement, U.S. Food & Drug Administration (FDA)
• Pure Base Distrbution Issues Allergy Alert on Undeclared Milk and Wheat in "Pure Base Garlic Spread - Concentrate" and "Pure Base Garlic Spread - Ready to Spread", U.S. Food & Drug Administration (FDA)
• Kellogg Company Voluntarily Recalls Select Packages of Kellogg's® Corn Pops®, Kellogg's® Honey Smacks®, Kellogg's® Froot Loops® and Kellogg's® Apple Jacks®, U.S. Food & Drug Administration (FDA)
• P&G Voluntarily Recalls 4 Hour Decongestant Nasal Spray in the United States, U.S. Food & Drug Administration (FDA)
• FDA Issues Draft Guidance on the Judicious Use of Medically Important Antimicrobials in Food-Producing Animals, U.S. Food & Drug Administration (FDA)
• FDA Approves Rapid Test for Antibodies to Hepatitis C Virus, U.S. Food & Drug Administration (FDA)
• Lancaster Foods, LLC Voluntarily Recalls Fresh Spinach with Best Enjoyed By Dates of June 19 to June 27, 2010 Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Anesthesiologist Sentenced on Health Care Fraud Charge, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Rapid blood test for antibodies to the hepatitis C virus (HCV) approved, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Issues Draft Guidance on the Judicious Use of Medically Important Antimicrobials in Food-Producing Animals, U.S. Food & Drug Administration (FDA)
• Two Recalls: Some Kellogg's Cereals and BBQ Chicken Pizza, U.S. Dept. of Health & Human Services
• H1N1 Influenza Public Health Emergency Determination to Expire on June 23, U.S. Dept. of Health & Human Services
• Office of Women's Health eUpdate, U.S. Food & Drug Administration (FDA)
• Two Recalls: Beef Products and Fresh Spinach, U.S. Dept. of Health & Human Services
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update, U.S. Food & Drug Administration (FDA)
• Advance Notice for Termination of the Emergency Use Authorization (EUA) of Medical Products and Devices, U.S. Dept. of Health & Human Services
• New CDC Test to Detect Human Infections with the 2009 H1N1 Influenza Virus Authorized for Use by FDA, U.S. Dept. of Health & Human Services
• Enforcement Report for June 23, 2010, U.S. Food & Drug Administration (FDA)
• Upcoming Webinar June 29th at 11:00 am ET: FDA Center for Tobacco Products Inaugural Year and Looking Forward, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Extends Comment Period on the Advanced Notice of Proposed Rulemaking for the Veterinary Feed Directive Regulation, U.S. Food & Drug Administration (FDA)
• Three New Recalls: Ground Beef and Pet Vitamins, U.S. Dept. of Health & Human Services
• Update of CVM's What's New - United Pet Group Voluntarily Recalls Pro-Pet Adult Daily Vitamin Supplement for Dogs Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• United Pet Group Voluntarily Recalls Pro-Pet Adult Daily Vitamin Supplement for Dogs Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA to Hold Daylong Meeting on Medical Device Innovation, U.S. Food & Drug Administration (FDA)
• FDA: Pfizer Voluntarily Withdraws Cancer Treatment Mylotarg from U.S. Market, U.S. Food & Drug Administration (FDA)
• Mylotarg (gemtuzumab ozogamicin): Market Withdrawal-Drug failed to demonstrate clinical benefit to patients enrolled in trials, FDA MedWatch
• RECALL: "Meat Without Feet" Lobster Claw & Knuckle Meat, U.S. Dept. of Health & Human Services
• FDA Marks First Anniversary of Tobacco Control Act, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Fourth Generation HIV Diagnostic Test Approved, permitting earlier detection of infection, U.S. Food & Drug Administration (FDA)
• Portland Shellfish Company Expands Recall to Include Meat Without Feet Label, Lobster Claw and Knuckle Meat, because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Approves First Diagnostic Assay to detect both HIV Antigen and Antibodies, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Natural Balance Pet Foods, Inc. announces a voluntary recall of Natural Balance Sweet Potato & Chicken Dry Dog Food Due to a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Magic Power Coffee: Undeclared Drug Ingredient - drug ingredient hydroxythiohomosildenafil may interact with prescription nitrates, and cause dangerously low blood pressure, FDA MedWatch
• PET FOOD RECALL: Natural Balance Sweet Potato & Chicken Dry Dog Food, U.S. Dept. of Health & Human Services
• Rich Products Corporation announces nationwide voluntary recall of Allen Bavarian Crème Filling due to undeclared allergens in product, U.S. Food & Drug Administration (FDA)
• Natural Balance Pet Foods, Inc. announces a voluntary recall of Natural Balance Sweet Potato & Chicken Dry Dog Food Due to a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers to Avoid Magic Power Coffee, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Warns Consumers to Avoid Magic Power Coffee, U.S. Dept. of Health & Human Services
• WHO Updates International H1N1 Flu Situation, U.S. Dept. of Health & Human Services
  • <Possible follow-ups>
  • WHO Updates International H1N1 Flu Situation, U.S. Dept. of Health & Human Services
• Update of CVM's What's New - Kent Nutrition Group, Inc. Conducts Nationwide Voluntary Recall of Kent Feeds Swine Products, U.S. Food & Drug Administration (FDA)
• RECALL: Marie Callender's Cheesy Chicken & Rice, Possible Salmonella, U.S. Dept. of Health & Human Services
• Kent Nutrition Group, Inc. Conducts Nationwide Voluntary Recall of Kent Feeds Swine Products, U.S. Food & Drug Administration (FDA)
• FDA Fines American Red Cross $16 Million for Prior Failures to Meet Blood Safety Laws, U.S. Food & Drug Administration (FDA)
• FDA Approves New Treatment for Advanced Prostate Cancer, U.S. Food & Drug Administration (FDA)
• FDA Approves New Indication for Tasigna, U.S. Food & Drug Administration (FDA)
• FDA Warns About Fraudulent Tamiflu, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Warns About Fraudulent Tamiflu, U.S. Dept. of Health & Human Services
• RECALL: Three Varieties of Spaghettios With Meatballs, U.S. Dept. of Health & Human Services
• Tamiflu: Counterfeit Product Sold on Internet - contains undeclared cloxacillin; risk for those allergic to penicillins, FDA MedWatch
• Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab[TM] Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab[TM] Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 16, 2010, U.S. Food & Drug Administration (FDA)
• NIH-Funded Scientists Find 2009 H1N1 Pandemic Influenza Vaccine Protects Mice from 1918 Influenza Virus, U.S. Dept. of Health & Human Services
• FDA to Host Public Meeting on Oversight of Laboratory-Developed Tests, U.S. Food & Drug Administration (FDA)
• Strengthening the Health Care Workforce Through the Affordable Care Act, U.S. Dept. of Health & Human Services
• FDA to Communicate Safety Monitoring Activities to Consumers and Health Care Professionals, U.S. Food & Drug Administration (FDA)
• May 2010 Drug Safety Labeling Changes: 23 Medical Product Labels with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• FDA Cautions on Accurate Vitamin D Supplementation for Infants, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vitamin D Supplement Products: Medication Use Error - Some liquid Vitamin D supplements sold with droppers that could allow harmful amounts of Vitamin D to be dispensed, FDA MedWatch
• Portland Shellfish Company Recalls Cooked, Frozen Claw Island Brand, Craig's All Natural Brand And Inland Ocean Brand Lobster Claw And Knuckle Meat Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Sirob Imports Issues Alert on Undeclared Sulfites in Strawberry Farms Sun Dried Tomatoes, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Sirob Imports Issues Alert on Undeclared Sulfites in Strawberry Farms Sun Dried Tomatoes, U.S. Dept. of Health & Human Services
• NOAA, FDA Continue Ramping Up Efforts to Ensure Safety of Gulf of Mexico Seafood, U.S. Food & Drug Administration (FDA)
• Kroger Recalls Select Containers of Deluxe Chocolate Paradise Ice Cream for Undeclared Allergen, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Kroger Recalls Select Containers of Deluxe Chocolate Paradise Ice Cream for Undeclared Allergen, U.S. Dept. of Health & Human Services
• Bimbo Bakeries USA, Inc. Announces Recall of Bimbo Soft White Bread Due To Undeclared Milk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Bimbo Bakeries USA, Inc. Announces Recall of Bimbo Soft White Bread Due To Undeclared Milk, U.S. Dept. of Health & Human Services
• Update of CVM's What's New - The Melamine Story, U.S. Food & Drug Administration (FDA)
• Former Colorado Springs Pharmacist Sentenced for Importation and Distribution of Chinese-Made Human Growth Hormones and Conspiracy to Distribute Anabolic Steroids, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Benicar (olmesartan) Ongoing Safety Review - FDA evaluating data in which type 2 diabetes patients taking Benicar had a higher rate of death from cardiovascular cause compared to placebo. FDA has not concluded that Benicar increases the risk of death., FDA MedWatch
• Domega NY International Co., LTD Issues Allergy Alert on Undeclared Egg in Fuma Custard Pie, U.S. Food & Drug Administration (FDA)
• FDA Seizes More Than $32,000 Worth of Bulk Honey from Philadelphia Distribution Center, U.S. Food & Drug Administration (FDA)
• Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
  • Vaccines and Related Biological Products Advisory Committee Update, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hospira Brand Liposyn and Propofol: Recall - Injectable products may contain particulate matter., FDA MedWatch
• FDA Advisory Panel to Review Dental Amalgam, U.S. Food & Drug Administration (FDA)
• How do I report a complaint about restaurant food?, U.S. Food & Drug Administration (FDA)
• How do I report a complaint about food bought in a supermarket?, U.S. Food & Drug Administration (FDA)
• How is the term "organic" regulated?, U.S. Food & Drug Administration (FDA)
• Does FDA have a definition for the term "organic" on food labels?, U.S. Food & Drug Administration (FDA)
• What is the meaning of 'natural' on the label of food?, U.S. Food & Drug Administration (FDA)
• If a food is labeled "organic" according to the USDA, is it still subject to the laws and regulations enforced by FDA?, U.S. Food & Drug Administration (FDA)
• Is Stevia an 'FDA approved' sweetener?, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - AHI Webinar - "Question-Based Review - Part II: Drug Product", U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - P&G Recalls Specific Canned Cat Foods Due to Low Levels of Thiamine (Vitamin B1), U.S. Food & Drug Administration (FDA)
• P&G Recalls Specific Canned Cat Foods Due to Low Levels of Thiamine (Vitamin B1), U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 9, 2010, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
  • U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Defibtech DBP-2800 Battery Packs used in Lifeline AED and ReviveR AED: Recall, FDA MedWatch
• Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility, U.S. Food & Drug Administration (FDA)
• West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Defibtech Announces a Voluntary Recall of DBP-2800 Battery Packs used in the Lifeline AED^®and ReviveR AED^TM, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New article for veterinarians on Preventing Medication Errors in Animals, U.S. Food & Drug Administration (FDA)
• Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - June 2010 FDA Patient Safety News now available, FDA MedWatch
• Eastern Fish Recalls Hannaford and Bloom Private Brand Frozen Raw Extra Jumbo Shrimp Packaged in 16 oz. Bags, Product of Mexico, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Eastern Fish Recalls Hannaford and Bloom Private Brand Frozen Raw Extra Jumbo Shrimp Packaged in 16 oz. Bags, Product of Mexico, U.S. Dept. of Health & Human Services
• FDA Takes Action Against California Soy-Product Manufacturer Lifesoy, U.S. Food & Drug Administration (FDA)
• How did the Federal Food, Drug, and Cosmetic Act come about?, U.S. Food & Drug Administration (FDA)
• When and why was FDA formed?, U.S. Food & Drug Administration (FDA)
• The June 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GammaGard Liquid, Immune Globulin Intravenous (Human): Market withdrawal due to reports of allergic reactions, FDA MedWatch
• WHO Director-General Statement on Continuation of Pandemic Disease, U.S. Dept. of Health & Human Services
• Enforcement Report for June 2, 2010, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Enforcement Report for June 2, 2010, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Minor Use Minor Species Drug Designation List Update, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Start of Generally Recognized as Safe (GRAS) Notification Pilot Program for Ingredients in Animal Food, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - May 2010 Green Book Update, U.S. Food & Drug Administration (FDA)
• FDA Basics Videos: Tim Cot&eacute; on Orphan Drugs, 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)
  • 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)
  • 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)
  • 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)
  • U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update, U.S. Food & Drug Administration (FDA)
• Preliminary Results: Surveillance for Guillain-Barre Syndrome After Receipt of Influenza A (H1N1) 2009 Monovalent Vaccine --- United States, 2009--2010, U.S. Dept. of Health & Human Services
• Kent Nutrition Group, Inc. Undertakes Limited Recall of Kent Feeds 20 Lamb DQ45 Medicated, U.S. Food & Drug Administration (FDA)
• Claris Lifesciences initiates a nationwide voluntary recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Aquaculture and Aquaculture Drugs Basics article, U.S. Food & Drug Administration (FDA)
• FDA Approves New Injectable Osteoporosis Treatment for Postmenopausal Women, U.S. Food & Drug Administration (FDA)
• The June 2010 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Selzentry (maraviroc) 150 mg and 300 mg tablets, labeling changes for patients with renal impairment, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 26, 2010, U.S. Food & Drug Administration (FDA)
• Better Made Snack Foods Issues an Allergy Alert on Undeclared Dairy in the 3-Ounce Better Made Special Original Potato Sticks, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Better Made Snack Foods Issues an Allergy Alert on Undeclared Dairy in the 3-Ounce Better Made Special Original Potato Sticks, U.S. Dept. of Health & Human Services
• Blacksmith Brands Announces Nationwide Voluntary Recall Of Four PediaCare Children's Products, U.S. Food & Drug Administration (FDA)
• PediaCare Children's Products [Blacksmith Brand]: Recall of four products - The four products were manufactured at a plant cited by FDA for deficiencies in Good Manufacturing Practices, FDA MedWatch
• Intravenous Medications Manufactured by Claris-Metronidazole, Ciprofloxacin and Ondansetron:Recall due to contamination of products, FDA MedWatch
• Hospira Announces an Expansion of a Nationwide Voluntary Recall of Certain Lots of Liposyn[TM] and Propofol That May Contain Particulate Matter, U.S. Food & Drug Administration (FDA)
• Fraud Prevention & The Affordable Care Act, U.S. Dept. of Health & Human Services
• Wally's Nut House, LLC Issues Allergy Alert on Undeclared Milk, Soy, and Wheat, U.S. Dept. of Health & Human Services
• Wally's Nut House, LLC ISSUES ALLERGY ALERT ON UNDECLARED MILK, SOY, AND WHEAT IN THE FOLLOWING PRODUCTS: "Tailgate Crunch Mix, Sweet Cajun Heat Mix, Country Western Mix, Cranberry Raisin Mix, Party Mix, Hot 'n Spicy Mix, and Louisiana Cajun Mix", U.S. Food & Drug Administration (FDA)
• organicgirl Produce Announces Limited Precautionary Recall of 10 oz organicgirl Baby Spinach with Use-by Date of May 22 Due to Possible Health Concern, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • organicgirl Produce Announces Limited Precautionary Recall of 10 oz organicgirl Baby Spinach with Use-by Date of May 22 Due to Possible Health Concern, U.S. Dept. of Health & Human Services
• HealthReform.gov Homepage Update, U.S. Dept. of Health & Human Services
  • <Possible follow-ups>
  • HealthReform.gov Homepage Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Homepage Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Homepage Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Homepage Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Homepage Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Homepage Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Homepage Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Homepage Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Homepage Update, U.S. Dept. of Health & Human Services
• Herb And Honey Issues Alert On Undeclared Sulfites In "Dried Apricots", U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Herb And Honey Issues Alert On Undeclared Sulfites In "Dried Apricots", U.S. Dept. of Health & Human Services
• FDA: Rare Cases of Liver Injury Reported with Use of Xenical, Alli, U.S. Food & Drug Administration (FDA)
• FDA Announces Collaboration with Drugs.com, U.S. Food & Drug Administration (FDA)
• So Shing Hing (USA) Trading Co Ltd Issues an Alert on Undeclared Sulfites in Dried Melon, U.S. Dept. of Health & Human Services
  • <Possible follow-ups>
  • So Shing Hing (USA) Trading Co Ltd Issues an Alert on Undeclared Sulfites in Dried Melon, U.S. Food & Drug Administration (FDA)
• Hylenex recombinant (hyaluronidase human injection): Recall - Voluntary recall of all manufactured lots has been initiated as a precautionary measure due to instances of particulate matter observed in a limited number of vials during routine stability testing., FDA MedWatch
• FDA MedWatch - Orlistat (marketed as Alli and Xenical): Labeling Change, FDA MedWatch
• Update of CVM's What's New - 2011: World Veterinary Year, U.S. Food & Drug Administration (FDA)
• HealthReform.gov Blog Update, U.S. Dept. of Health & Human Services
  • <Possible follow-ups>
  • HealthReform.gov Blog Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Blog Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Blog Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Blog Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Blog Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Blog Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Blog Update, U.S. Dept. of Health & Human Services
  • HealthReform.gov Blog Update, U.S. Dept. of Health & Human Services
• FDA: Possible Fracture Risk with High Dose, Long-term Use of Proton Pump Inhibitors, U.S. Food & Drug Administration (FDA)
• Western District of Wisconsin Announces Consent Decree Between Beehive Botanicals and the United States, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Proton Pump Inhibitors (PPI): Class Labeling Change, FDA MedWatch
• FDA Approves New Treatment for Late-Onset Pompe Disease, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ultram (tramadol hydrochloride), Ultracet (tramadol hydrochloride/acetaminophen): Label Change, FDA MedWatch
• Medicare & the Affordable Care Act, U.S. Dept. of Health & Human Services
• Fresh Express Recalls Romaine-based Salads with Use-by Dates of May 13-16th Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Fresh Express Recalls Romaine-based Salads with Use-by Dates of May 13-16th Due to Possible Health Risk, U.S. Dept. of Health & Human Services
• FoodSafety.gov News & Events Update, U.S. Dept. of Health & Human Services
  • <Possible follow-ups>
  • FoodSafety.gov News & Events Update, U.S. Dept. of Health & Human Services
  • FoodSafety.gov News & Events Update, U.S. Dept. of Health & Human Services
  • FoodSafety.gov News & Events Update, U.S. Dept. of Health & Human Services
  • FoodSafety.gov News & Events Update, U.S. Dept. of Health & Human Services
  • FoodSafety.gov News & Events Update, U.S. Dept. of Health & Human Services
• Weekly FluView Map and Surveillance Report for the Week Ending May 15, 2010, U.S. Dept. of Health & Human Services
• FDA Clears First 2009 H1N1 Influenza Virus Test Previously Available Under Emergency Use Authorization, U.S. Dept. of Health & Human Services
• Update of CVM's What's New - FDA and NIH Launch Electronic Safety Reporting Portal, U.S. Food & Drug Administration (FDA)
• Genzyme Corp. Signs Consent Decree to Correct Violations at Allston, Mass., Manufacturing Plant and Give up $175 Million in Profits, U.S. Food & Drug Administration (FDA)
• FDA and NIH Launch Electronic Safety Reporting Portal, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces the Availability of Electronic Submissions for Animal Drug Adverse Events/New Guidance Available, U.S. Food & Drug Administration (FDA)
• Watch: FDA Basics Videos, U.S. Food & Drug Administration (FDA)
• How many people are employed by FDA and in what areas do they work?, U.S. Food & Drug Administration (FDA)
• Ortho-McNeil Pharmaceutical, LLC Pleads Guilty to Illegal Promotion of Topamax and is Sentenced to Criminal Fine of $6.14 Million, U.S. Food & Drug Administration (FDA)
• FDA Clears First 2009 H1N1 Influenza Virus Test Previously Approved for Emergency-Use Only, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA Basics Updates - Webinar on May 26 at 2:00pm ET, U.S. Food & Drug Administration (FDA)
• Caldwell Fresh Foods Recalls Alfalfa Sprouts Because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
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