FDA News Releases

• Date Index

• Drug Shortages Update, (continued)
  • Drug Shortages Update, U.S. Food & Drug Administration (FDA)
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• Urgent Nationwide Alfalfa Sprout Recall, U.S. Dept. of Health & Human Services
  • <Possible follow-ups>
  • Urgent Nationwide Alfalfa Sprout Recall, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - June 10-11, 2010 Advisory Committee meeting re: policy on deferral of donors with high-risk exposure to HIV, U.S. Food & Drug Administration (FDA)
• CORRECTION: Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Milk in "Gourmet Cookie Mixes", U.S. Dept. of Health & Human Services
• Voluntary Recall of HYLENEX Initiated, U.S. Food & Drug Administration (FDA)
• How do I discard medicine that I no longer need, do I just throw it in the garbage?, U.S. Food & Drug Administration (FDA)
• What are unapproved drugs and why are they on the market?, U.S. Food & Drug Administration (FDA)
• Vanlaw Food Products, Inc. Announces Voluntary Recall of Valu Time Brand Ranch Dressing, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Vanlaw Food Products, Inc. Announces Voluntary Recall of Valu Time Brand Ranch Dressing, U.S. Dept. of Health & Human Services
• Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Milk in "Gourmet Cookie Mixes", U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Milk in "Gourmet Cookie Mixes", U.S. Dept. of Health & Human Services
• Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Egg in "Peanut Butter Spread", U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Rise 'N Roll Bakery Issues Allergy Alert on Undeclared Egg in "Peanut Butter Spread", U.S. Dept. of Health & Human Services
• Drug Information Update - FDA Launches Initiative to Reduce Infusion Pump Risks, U.S. Food & Drug Administration (FDA)
• FDA Launches Initiative to Reduce Infusion Pump Risks, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 21, 2010, U.S. Food & Drug Administration (FDA)
• LIFEPAK 15 Monitor/Defibrillator by Physio-Control Inc.-Class I Recall, FDA MedWatch
• CVM Updates - FDA Announces Minor Use/Minor Species (MUMS) Grant Program Request for Applications, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CVM Updates - FDA Announces Minor Use/Minor Species (MUMS) Grant Program Request for Applications, U.S. Food & Drug Administration (FDA)
  • CVM Updates - FDA Announces Minor Use/Minor Species (MUMS) Grant Program Request for Applications, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Announces Draft Revised Guidance on Transparency and Advisory Committees, U.S. Food & Drug Administration (FDA)
• Propylthiouracil-Boxed Warning Added, FDA MedWatch
• Federal Prisoner Serving Time for Health Care Fraud Charged with Distributing Misbranded Drugs that were Labeled as "All Natural" Sexual Enhancement, U.S. Food & Drug Administration (FDA)
• Buckley Woman Sentenced to Jail Time, Home Detention for False Claim of Glass in Bottled Water, U.S. Food & Drug Administration (FDA)
• Drug Information Update - New Boxed Warning on severe liver injury with propylthiouracil, U.S. Food & Drug Administration (FDA)
• FDA Announces Draft Revised Guidance on Transparency and Advisory Committees, U.S. Food & Drug Administration (FDA)
• Generic Drug Roundup: April 2010, U.S. Food & Drug Administration (FDA)
• FDA Obtains Consent Decree to Stop Marketing of Unapproved Sterilization System, U.S. Food & Drug Administration (FDA)
• No Bones About It: Bones are Unsafe for Your Dog, U.S. Food & Drug Administration (FDA)
• FDA Statement on IOM Sodium Report, U.S. Food & Drug Administration (FDA)
• FDA to Address Challenges of Using Complex Medical Devices in the Home, U.S. Food & Drug Administration (FDA)
• Upcoming Webinar on Thursday, April 22--Safeguarding the U.S. Food Supply: Excellent Industry Compliance With the Bovine Spongiform Encephalopathy (BSE) Final Rule, U.S. Food & Drug Administration (FDA)
• Purina Mills Undertakes Limited Recall of Strategy® Horse Feed and Layena® Poultry Feed, U.S. Food & Drug Administration (FDA)
• FDA Seeks Injunction Against Florida Animal Drug Compounder, U.S. Food & Drug Administration (FDA)
• FDA Launches Medical Device and Radiation-Emitting Product Transparency Web site, U.S. Food & Drug Administration (FDA)
• ***CONSUMER ALERT*** Undeclared Sulfites in "Nut Tree Health Mix", U.S. Food & Drug Administration (FDA)
• StarKist Co. Initiates Limited Regional Voluntary Recall of Two SeaSations® Products Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• FDA Issues Guidance on New Safety Rules for Shell Eggs, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 14, 2010, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - March 2010 Drug Safety Labeling Changes: 40 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• My-A & Co, Recalls Ground Black Pepper Double Golden Fish 3.5oz Jars Due to Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Atlas Operations, Inc. Announces Expansion of its Nationwide Voluntary Recall of Specific Lots of Sexual Enhancement Products Marketed as Dietary Supplements, U.S. Food & Drug Administration (FDA)
• Response Products Voluntarily Recalls Advanced Cetyl M Joint Action Formula for Dogs Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Asthma and COPD Inhalers That Contain Ozone-depleting CFCs to be Phased Out; Alternative Treatments Available, U.S. Food & Drug Administration (FDA)
• Seven Inhalers That Use CFCs Being Phased Out, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Approves Pancreatic Enzyme Product, Pancreaze, U.S. Food & Drug Administration (FDA)
• FDA Approves Pancreatic Enzyme Product, Pancreaze, U.S. Food & Drug Administration (FDA)
• FDA's MedWatch Safety Alerts: March 2010, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Holds Public Meeting on Prescription Drug User Fee Act, U.S. Food & Drug Administration (FDA)
• Consumer Alert Precautionary Recall issued for H-E-B French Onion Dip, U.S. Food & Drug Administration (FDA)
• FDA Holds Public Meeting on Prescription Drug User Fee Act, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Public Meeting on the National Antimicrobial Resistance Monitoring System (NARMS), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - April 2010 FDA Patient Safety News now available, FDA MedWatch
• Drug Information Update: FDA Provides Information to Consumers about the Ingredient Triclosan, U.S. Food & Drug Administration (FDA)
• Mccormick & Company Recalls Mccormick Fajitas Seasoning Mix Due To Unlabeled Wheat And Milk Ingredients, U.S. Food & Drug Administration (FDA)
• FDA Provides Information to Consumers about Triclosan, U.S. Food & Drug Administration (FDA)
• Triclosan: What Consumers Should Know, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Approves First Generic Versions of Two Drugs for the Treatment of Hypertension, U.S. Food & Drug Administration (FDA)
• FDA Approves First Generic Versions of Two Drugs for the Treatment of Hypertension, U.S. Food & Drug Administration (FDA)
• Camolyn eye drops, Fisiolin nasal drops: Voluntary recall :Lack of sterile product has the potential to cause infections, FDA MedWatch
• Stud Capsule For Men: Product adulterated with sildenafil which may interact with nitrates to lower blood pressure to dangerous levels, FDA MedWatch
• US Oftalmi Announces Voluntary Recall of the Camolyn Eye Drops Product Line, and Fisiolin Nasal Drops. Includes All Lots of 15mL Bottles., U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 7, 2010, U.S. Food & Drug Administration (FDA)
• FDA Warns About Lipodissolve Product Claims, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Issues Warning Letters for Drugs Promoted in Fat Elimination Procedure, U.S. Food & Drug Administration (FDA)
• FDA Issues Warning Letters for Drugs Promoted in Fat Elimination Procedure, U.S. Food & Drug Administration (FDA)
• Medical Device Manufacturer Guidant Pleads Guilty for not Reporting Defibrillator Safety Problems to FDA, U.S. Food & Drug Administration (FDA)
• Drug Information Update: Follow up to the Public Health Alert about Changes to the Heparin Sodium USP Monograph, U.S. Food & Drug Administration (FDA)
• Kroger Recalls Two Seasonings Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Del Bueno Recalls Queso Fresco Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Del Bueno Amends Recall of Queso Fresco Cheese Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kanec USA Inc., Issues a Voluntary Nationwide Recall of Stud Capsule For Men Marketed as Dietary Supplements, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Voluntarily Recalls Frozen Whole Catch Yellow Fin Tuna Steaks Due to Possible Health Risks, U.S. Food & Drug Administration (FDA)
• FDA Approves New Formulation for OxyContin, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves New Formulation for OxyContin, U.S. Food & Drug Administration (FDA)
• FDA Approves First Biodegradable Sealant Patch for Cardiovascular Surgery, U.S. Food & Drug Administration (FDA)
• Federal Government Seizes Dozens of Misbranded Drug Products, U.S. Food & Drug Administration (FDA)
• CVM Updates - March 2010 Update on Feed Enforcement Activities to Limit the Spread of BSE, U.S. Food & Drug Administration (FDA)
• Golden Pacific Foods, Inc. Issues Allergy Alert for Undeclared Milk and Soy in Marco Polo Brand Shrimp Snacks, U.S. Food & Drug Administration (FDA)
• NY Gourmet Salads Inc. Recalls Chick Pea Salad Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Consumer Representatives Needed for FDA Advisory Committees: Learn More at Public Meeting, U.S. Food & Drug Administration (FDA)
• Glutino Food Group Issues Allergy Alert on Undeclared Egg Product in Raisin Bread, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 31, 2010, U.S. Food & Drug Administration (FDA)
• Zatarain's Recalls Original Dirty Rice Mix Package Due to Unlabeled Wheat and Barley Ingredients, U.S. Food & Drug Administration (FDA)
• Watkins Incorporated Recalls Crab Snack & Dip Seasoning Because of Possible Health Risk from Ingredient Supplied by Kerry Ingredients, U.S. Food & Drug Administration (FDA)
• Federal Government Seeks Permanent Injunction Against Texas Egg Roll Manufacturer, U.S. Food & Drug Administration (FDA)
• FDA Requires Device Manufacturers to Include Information on Pediatric Populations, U.S. Food & Drug Administration (FDA)
• Stalevo (entacapone/carbidopa/levodopa): Ongoing Safety Review, FDA MedWatch
• Drug Information Update - Ongoing Safety Review of Stalevo (entacapone/carbidopa/levodopa) and possible development of Prostate Cancer, U.S. Food & Drug Administration (FDA)
• Binell Bros. Cutlery Voluntarily Recalls Black Pepper, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves Asclera to Treat Small Varicose Veins, U.S. Food & Drug Administration (FDA)
• MasXtreme Capsules (Natural Wellness) - product contains undeclared drug ingredient, FDA MedWatch
• FDA Approves Asclera to Treat Small Varicose Veins, U.S. Food & Drug Administration (FDA)
• Natural Wellness, Inc. Issues a Nationwide Voluntary Recall of Masxtreme Capsules, Marketed As a Dietary Supplement, U.S. Food & Drug Administration (FDA)
• Modern Products recalls Seasonings due to possible health risk, U.S. Food & Drug Administration (FDA)
• Perfect Candy & Packaging Co. Announces a Voluntary Nationwide Recall of Whole Black Pepper in H.D.W. FOODS Labeled Bags, U.S. Food & Drug Administration (FDA)
• Medications for Your Pet: 10 Questions to Ask Your Vet, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Solicits Comments Related to Veterinary Feed Directive (VFD) Drugs, U.S. Food & Drug Administration (FDA)
• Public Health Agencies Collaborate to Prevent Further Illnesses from Norovirus Outbreak Associated with Oysters Recently Harvested from Area Near Port Sulphur, La., U.S. Food & Drug Administration (FDA)
• Two Arrested for Illegally Trafficking Counterfeit Weight Loss Medication, U.S. Food & Drug Administration (FDA)
• Public Health Agencies Warn of Outbreaks Related to Drinking Raw Milk, U.S. Food & Drug Administration (FDA)
• FDA Takes Action Against New York Dairy Farmer, U.S. Food & Drug Administration (FDA)
• Obstetrics Manager Convicted of Tampering with Patient's Narcotics Medicines at White Salmon Hospital, U.S. Food & Drug Administration (FDA)
• C. H. Guenther & Son, Inc. Announces Voluntary Nationwide Recall of Chilli Man Seasoning Mix due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• C. H. Guenther & Son, Inc. Announces Amended Voluntary Nationwide Recall of several additional products that contain pepper due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves New Use of Xifaxan for Patients with Liver Disease, U.S. Food & Drug Administration (FDA)
• FDA Approves New Use of Xifaxan for Patients with Liver Disease, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 24, 2010, U.S. Food & Drug Administration (FDA)
• Blue Line Foodservice Distribution voluntarily recalls "Spice Paks", U.S. Food & Drug Administration (FDA)
• Walong Marketing, Inc. Expands Nationwide Voluntary Recall Flying Horse Sesame Chewy Candy Due to Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• C. H. Guenther & Son, Inc. Announces Amended Voluntary Nationwide Recall of several products that contain pepper due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• McCain Foods USA Announces Voluntary Recall of Frozen Potato Product Containing Black Pepper That May Pose Health Risk, U.S. Food & Drug Administration (FDA)
• Rotarix Vaccine: Recommendation to suspend use-Precaution while FDA learns more about the situation. No known safety risk at this time, FDA MedWatch
• U.S. Attorney News Release: Three Indicted for Diversion of Prescription Drugs, U.S. Food & Drug Administration (FDA)
• Components of Extraneous Virus Detected in Rotarix Vaccine; No Known Safety Risk, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Drug Info: Drug Safety Podcasts for Healthcare Professionals, U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Springfield (Missouri) Business Owner Pleads Guilty to $17 Million Fraud Scheme, U.S. Food & Drug Administration (FDA)
• John B. Sanfilippo & Son, Inc. Voluntarily Recalls Snack Mix and Cashew Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Upcoming Webinar on FDA's Inspection Process, U.S. Food & Drug Administration (FDA)
• Boston Scientific Implantable Cardioverter Defibrillators:Recall-Practitioners should not use devices unless, until FDA reviews, approves changes made by the manufacturer, FDA MedWatch
• Zocor (simvastatin): increased risk of muscle injury with high doses-risk also increased when drug, especially at higher doses, is used with certain drugs, FDA MedWatch
• Kroger Amends Code Date on Recalled Seasoning Blend Garlic Powder, U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Warns about Increased Risk of Muscle Injury with Zocor, U.S. Food & Drug Administration (FDA)
• FDA Warns about Increased Risk of Muscle Injury with Zocor, U.S. Food & Drug Administration (FDA)
• Becton, Dickinson (BD) Q-Syte Luer Access Split Septum Device: Class I Recall-Defective devices may result in air bubbles leaking into the infusion system and into the patient's bloodstream, FDA MedWatch
• Drug Information Update- FDA Approves Carbaglu Tablets to Treat Condition That Causes Elevated Ammonia Levels., U.S. Food & Drug Administration (FDA)
• FDA Approves Drug to Treat Condition That Causes Elevated Ammonia Levels, U.S. Food & Drug Administration (FDA)
• FDA Issues Final Rule Restricting Access and Marketing of Cigarettes and Smokeless Tobacco Products to Youth, U.S. Food & Drug Administration (FDA)
• Cleviprex (clevidipine butyrate): Recall of 12/2009 expanded to additional lots; Presence of particulate matter could reduce blood flow..., FDA MedWatch
• Enforcement Report for March 17, 2010, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Enforcement Report for March 17, 2010, U.S. Food & Drug Administration (FDA)
• Barcel Announces Voluntary Recall, U.S. Food & Drug Administration (FDA)
• Produce Valley, Inc. Initiates Voluntary Recall Due to Possible Health Risk Associated with Recalled Hydrolyzed Vegetable Protein (HVP) by Basic Food Flavors, Inc., U.S. Food & Drug Administration (FDA)
• Statement for National Poison Prevention Week, U.S. Food & Drug Administration (FDA)
• Spice Barn, Inc. Voluntarily Recalls Two Lots of Black Pepper, U.S. Food & Drug Administration (FDA)
• The Medicines Company Expands a Nationwide Recall for Certain Lots of Cleviprex® That May Contain Particulate Matter, U.S. Food & Drug Administration (FDA)
• C. H. Guenther & Son, Inc. Announces Voluntary Nationwide Recall of several products that contain pepper due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Gyrus ACMI Micron Bobbin Vent Tube T: Class I Recall-Device implanted for ventilation or drainage of the middle ear - shipped without being sterilized, FDA MedWatch
• FDA Approves First Totally Implanted Hearing System, U.S. Food & Drug Administration (FDA)
• FDA's MedWatch Safety Alerts: February 2010, U.S. Food & Drug Administration (FDA)
• FDA Seeks Permanent Injunction Against Louisiana Sprout Grower, U.S. Food & Drug Administration (FDA)
• FDA March 17 Update on the Investigation into the Salmonella Montevideo Outbreak, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Orders 2 Companies to Stop Marketing Unapproved Nitroglycerin Tablets, U.S. Food & Drug Administration (FDA)
• FDA Orders 2 Companies to Stop Marketing Unapproved Nitroglycerin Tablets, U.S. Food & Drug Administration (FDA)
• GFN Foods, LLC Voluntarily Recalls Gluten-Free Naturals Pancake Mix, Gluten-Free Naturals Light & Moist Yellow Cake Mix and Gluten-Free Naturals Cookie Blend Flour, U.S. Food & Drug Administration (FDA)
• Emmi - Roth Käse USA Announces Recall of Spreadables brand Crab Creole and Shrimp Scampi Cheese Spreads, U.S. Food & Drug Administration (FDA)
• Teleflex Arrow IV Tubing Sets, Accessories, and Embolectomy Catheters: Recall, FDA MedWatch
• Start at the Store: Prevent Foodborne Illness (video), U.S. Food & Drug Administration (FDA)
• Tastefully Simple Issues Voluntary Recall for Toasted Garlic & Parmesan Cheese Ball Mix, U.S. Food & Drug Administration (FDA)
• Teleflex Incorporated Announces Worldwide Voluntary Recall of Arrow Select IV Tubing Sets, Accessories, and Certain Embolectomy Catheters, U.S. Food & Drug Administration (FDA)
• Julia's Spices Inc Recalls Hulled Sesame Seeds Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Spice Industrial Inc. Recalls Lian How White Sesame Seeds Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Drug Information Update: Statement to Healthcare Professionals on the ACCORD Lipid Trial, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 10, 2010, U.S. Food & Drug Administration (FDA)
• Plavix (clopidogrel): Boxed warning added regarding reduced effectiveness of Plavix in poor metabolizers, FDA MedWatch
• Counterfeit Polypropylene Surgical Mesh: Counterfeit flat sheets of product are being marketed US, labeled with Bard/Davol brand name, FDA MedWatch
• FDA Announces New Boxed Warning on Plavix, U.S. Food & Drug Administration (FDA)
• Drug Information Update - Reduced effectiveness of Plavix (clopidogrel) in patients who are poor metabolizers of the drug, U.S. Food & Drug Administration (FDA)
• FDA Task Force Seeks Public Comments on Increasing Transparency with Regulated Industry, U.S. Food & Drug Administration (FDA)
• Austinuts Of Dallas, Inc. Announces Voluntary Recall of Honey Mustard Pretzels, U.S. Food & Drug Administration (FDA)
• McCormick Recall Due to Possible Health Risk from HVP Ingredient Expands to Include Additional "Best By" Dates, U.S. Food & Drug Administration (FDA)
• FDA Issues Warning on Counterfeit Surgical Mesh, U.S. Food & Drug Administration (FDA)
• Abiomed AB5000 Circulatory Support System: Class I Recall-Device computer may shut down without an alarm, which can lead to serious injuries or death, FDA MedWatch
• Baylis Medical Torflex Transseptal Guiding Sheath: Class I Recall- tip may break off, separate during procedures, could lead to permanent injury and/or death, FDA MedWatch
• Oral Bisphosphonates:Ongoing Safety Review of Atypical Subtrochanteric Femur Fractures-have not shown clear connection between bisphosphonates, risk of fracture, FDA MedWatch
• Beckman Coulter UniCel DxC Synchron Clinical System - Ion Selective Electrode Flow Cell: Class I Recall-Incorrect sodium results due to build-up of protein, bacteria, in the flow cell, FDA MedWatch
• FDA March 11 Update on the Investigation into the Salmonella Montevideo Outbreak, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - February 2010 Drug Safety Labeling Changes: 24 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• Orval Kent Food Company, Inc. Voluntarily Recalls Culinary Circle Dips Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Frontier Natural Products Co-op Initiates Voluntary Recall Due to Possible Health Risk from Black Pepper, U.S. Food & Drug Administration (FDA)
• Olde Westport Spice Announces a Voluntary Recall of Garden Harvest Special Blend Seasoning, U.S. Food & Drug Administration (FDA)
• Mrs. Gerry's Kitchen Press Release, U.S. Food & Drug Administration (FDA)
• Quaker Snack Mix Baked Cheddar Voluntarily Recalled Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Mrs. Gerry's Kitchen Press Release., U.S. Food & Drug Administration (FDA)
• Kroger Recalls Two Onion Soup & Dip Mixes Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Ventura Foods, LLC Voluntarily Recalls Seven Varieties of Its Dean's® Dip Products As A Precautionary Measure, U.S. Food & Drug Administration (FDA)
• Publix Issues Voluntary Recall on Four Seasoning Mixes, U.S. Food & Drug Administration (FDA)
• P&G Joins Industry Ingredient Recall by Voluntarily Recalling Two Flavors of Pringles® in the United States in Response to FDA Industry Guidance, U.S. Food & Drug Administration (FDA)
• Drug Information Update - Ongoing safety review of oral bisphosphonates and atypical subtrochanteric femur fractures, U.S. Food & Drug Administration (FDA)
• WinRho SDF (Rho(D) Immune Globulin Intravenous (Human): Risk of intravascular hemolysis in patients treated for immune thrombocytopenic purpura, FDA MedWatch
• Nutritional Resources Announces a Nationwide Voluntary Recall of Healthwise Cream of Mushroom Soup Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• GNS Foods Voluntarily Recalls Snack Mixes Containing Honey Mustard/Onion Pretzels from National Pretzel Co. associated with Hydrolyzed Vegetable Protein (HVP) recalled by Basic Food Flavors, Inc. because of the potential Salmonella contamination., U.S. Food & Drug Administration (FDA)
• Herr Foods Inc. Recalls 'Herr's Cracked Pepper and Sea Salt Flavored' Kettle Style Potato Chips Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Dutch Valley Food Distributors, Inc. Announces a Voluntary Nationwide Recall of Black Pepper and Products made with Black Pepper, U.S. Food & Drug Administration (FDA)
• FDA Approves Botox to Treat Spasticity in Flexor Muscles of the Elbow, Wrist and Fingers, U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Approves Botox to Treat Spasticity in Flexor Muscles of the Elbow, Wrist and Fingers, U.S. Food & Drug Administration (FDA)
• Nature's Variety Expands Nationwide Voluntary Recall to Include All Raw Frozen Chicken Diets with Any "Best If Used By" Date On or Before 2/5/11, U.S. Food & Drug Administration (FDA)
• Estrella Family Creamery Recalls Old Apple Tree Tomme Cheese Due to Possible Health Risks, U.S. Food & Drug Administration (FDA)
• National Pretzel Co. Annouces Precautionary Recall of Honey Mustard Onion Seasoned Pretzels Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Ed Roller, Inc. Announces Voluntary Recall of Wegmans 9 oz. Food You Feel Good About® Medium Seafood Sauce Due to Undeclared Ingredients on Label, U.S. Food & Drug Administration (FDA)
• Fresh Food Concepts Announces a Voluntary Recall of Spinach Dips Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• McCormick & Company Initiates Recall Due to Possible Health Risk from HVP Ingredient, U.S. Food & Drug Administration (FDA)
• Creative Contract Packaging Corporation Recalls HERB-OX® Bouillon Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Mincing Overseas Spice Company Voluntarily Recalls Two Lots of Black Pepper, U.S. Food & Drug Administration (FDA)
• FDA Update on the Investigation into the Salmonella Montevideo Outbreak - March 5, 2010, U.S. Food & Drug Administration (FDA)
• Concord Foods Recalls Concord Foods Seasonings Mixes because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Thomas Medical Products, Inc., Transseptal Sheath Introducer Kits: Class I Recall, FDA MedWatch
• Recall of Hydrolyzed Vegetable Protein, U.S. Food & Drug Administration (FDA)
• FDA Investigation Reveals Salmonella Tennessee at Plant that Makes Flavor Enhancers for Food Processors and Other Distributors, U.S. Food & Drug Administration (FDA)
• FDA Approves Name Change for Heartburn Drug Kapidex, U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Approves Name Change for Heartburn Drug Kapidex, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - March 2010 FDA Patient Safety News now available, FDA MedWatch
• Baxter HomeChoice and HomeChoice PRO Automated Peritoneal Dialysis Systems: Class I Recall. Reports of serious injuries associated with increased Intraperitoneal Volume, FDA MedWatch
• Reser's Fine Foods Inc Press Release, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Warns Consumers in Puerto Rico of Harmful Bacteria in Hand Sanitizers, U.S. Food & Drug Administration (FDA)
• Earth Island Announces Voluntary Recall On Select Follow Your Heart Products That Contain Natural Flavor Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Homemade Gourmet Voluntarily Recalls "Tortilla Soup Mix" Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers in Puerto Rico of Harmful Bacteria in Hand Sanitizers, U.S. Food & Drug Administration (FDA)
• FDA, FSIS, CDC Collaborate on Methods to Measure Success of Food Safety Programs, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 3, 2010, U.S. Food & Drug Administration (FDA)
• FDA Calls on Food Companies to Correct Labeling Violations; FDA Commissioner Issues an Open Letter to the Industry, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 24, 2010, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves First Generic Tamsulosin to Treat Enlarged Prostate Gland, U.S. Food & Drug Administration (FDA)
• Castella Imports, Inc. Conducts Nationwide Recall of Castella Chicken Soup Base Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Survey Finds More Americans Read Information on Food Labels, U.S. Food & Drug Administration (FDA)
• FDA Approves First Generic Tamsulosin to Treat Enlarged Prostate Gland, U.S. Food & Drug Administration (FDA)
• Survey Shows Gains in Food-Label Use, Health/Diet Awareness, U.S. Food & Drug Administration (FDA)
• T. Marzetti Company Announces a Voluntary Recall of Dips Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Boca Raton Man Sentenced for Nutritional Supplement Scam, U.S. Food & Drug Administration (FDA)
• Heartland Foods, Inc. voluntarily recalls Coarse Ground Black Pepper because of possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA Announces Meeting Information and Voting Membership of the Tobacco Products Scientific Advisory Committee, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves Therapy to Treat Gaucher Disease, U.S. Food & Drug Administration (FDA)
• American Pecan Co. Recalls Pecans Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Johnny's Fine Foods Recalls Johnny's French Dip Powdered Au Jus Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• International Collaboration: FDA and European Medicines Agency Agree to Accept a Single Orphan Drug Designation Annual Report, U.S. Food & Drug Administration (FDA)
• FDA Approves Therapy to Treat Gaucher Disease, U.S. Food & Drug Administration (FDA)
• FDA Update on the Investigation into the Salmonella Montevideo Outbreak - February 26, 2010, U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Medical Device Manufacturer Guidant Charged in Failure to Report Defibrillator Safety, U.S. Food & Drug Administration (FDA)
• OneTouch SureStep Test Strips: Recall-Test strips may provide falsely low results when glucose level is over 400 mg/dL, FDA MedWatch
• StatSpin Express 4 Centrifuges: Recall- Rotor may break, eject pieces of the rotor, may cause serious physical injury, expose to blood-borne infectious micro-organisms, FDA MedWatch
• Thumb Oilseed Recalls Soy Grits and Flour Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• LifeScan Recalls Specific Lots of Consumer and Professional OneTouch® SureStep® Test Strips Due To Inaccurate, U.S. Food & Drug Administration (FDA)
• Wholesome Spice Recalls 25 Lb. Boxes Of Crushed Red Pepper Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Update on the Investigation into the Salmonella Montevideo Outbreak - February 25, 2010, U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Medical Technician Sentenced to 30 Years, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 24, 20104, U.S. Food & Drug Administration (FDA)
• Maryland Veal Calf Dealer Agrees to Close in Response to FDA-Initiated Action, U.S. Food & Drug Administration (FDA)
• FDA Approves Pneumococcal Disease Vaccine with Broader Protection, U.S. Food & Drug Administration (FDA)
• Drug Information Update: Mifeprex Questions and Answers, U.S. Food & Drug Administration (FDA)
• NIH and FDA Announce Collaborative Initiative to Fast-track Innovations to the Public, U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Woman pleads guilty to poisoning salsa at Lenexa restaurant, U.S. Food & Drug Administration (FDA)
• Reporting Problems to FDA (video), U.S. Food & Drug Administration (FDA)
• Invirase (saquinavir): Ongoing safety review of clinical trial data-Possible association with abnormal heart rhythms when used in combination with Norvir (ritonavir), FDA MedWatch
• FDA Announces Possible Safety Concern for HIV Drug Combination, U.S. Food & Drug Administration (FDA)
• Drug Information Update - Ongoing safety review of Invirase (saquinavir) and possible association with abnormal heart rhythms, U.S. Food & Drug Administration (FDA)
• Safety Review of Avandia (Rosiglitazone), U.S. Food & Drug Administration (FDA)
• Avandia (rosiglitazone): FDA reviewing a large, long-term clinical study on possible risks for cardiovascular outcomes with use of rosiglitazone, FDA MedWatch
• Drug Information Update: Ongoing review of Avandia (rosiglitazone) and cardiovascular safety, U.S. Food & Drug Administration (FDA)
• Fresh & Easy Neighborhood Market Voluntarily Recalls Fresh & Easy Chewy Chocolate Chip Granola Bars Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Lovin Oven LLC Voluntarily Recalls Certain Health Valley® Organic Peanut Crunch, Dutch Apple and Wildberry Chewy Granola Bars, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Lovin Oven LLC Voluntarily Recalls Certain Health Valley® Organic Peanut Crunch, Dutch Apple and Wildberry Chewy Granola Bars, U.S. Food & Drug Administration (FDA)
• Queseria Bendita Recalls Queso Fresco, Panela, and Requeson Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Regulatory Science Update: FDA and International Serious Adverse Events Consortium Complete Third Data Release, U.S. Food & Drug Administration (FDA)
• U.S. Attorney New Release: Miami Prescription Drug Diverter Sentenced To 70 Months In Prison, U.S. Food & Drug Administration (FDA)
• Ear Candles: Risk of Serious Injuries-Consumers warned not to use ear candles because they can cause burns, perforation, blockage, FDA MedWatch
• Upcoming Webinar to Inform Public About Access to Investigational Drugs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - January 2010 Drug Safety Labeling Changes: 36 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• Drug Information Update- February 28, 2010 Deadline to Submit Comments on "Promotion of FDA-Regulated Medical Products Using the Internet and Social Media Tools", U.S. Food & Drug Administration (FDA)
• U.S. Attorney New Release: SK Foods former owner charged with RICO violations, U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Approves Rituxan to Treat Chronic Lymphocytic Leukemia, U.S. Food & Drug Administration (FDA)
• FDA Cancer Drug Approval Rate Highlighted in JNCI, U.S. Food & Drug Administration (FDA)
• FDA Approves Rituxan to Treat Chronic Lymphocytic Leukemia, U.S. Food & Drug Administration (FDA)
• USDA and FDA Coordinating Efforts to Ensure Safety of Produce, U.S. Food & Drug Administration (FDA)
• Long-Acting Beta-Agonists (LABAs): New Safe Use Requirements-FDA requires risk management plan and class-labeling changes for all LABAs, FDA MedWatch
• Don't Get Burned: Stay Away From Ear Candles, U.S. Food & Drug Administration (FDA)
• FDA Urges Safe Use of Certain Inhaled Asthma Medicines, U.S. Food & Drug Administration (FDA)
• Exjade (deferasirox): Boxed Warning - Changes to Prescribing Information re: risk of renal impairment/failure, hepatic impairment/failure or gastrointestinal hemorrhage, FDA MedWatch
• FDA Announces New Safety Controls for Long-Acting Beta Agonists, Medications Used to Treat Asthma, U.S. Food & Drug Administration (FDA)
• Drug Information Update - New safety requirements for long-acting inhaled asthma medications called Long-Acting Beta-Agonists (LABAs), U.S. Food & Drug Administration (FDA)
• Estrella Family Creamery Expands Recall Of Various Cheeses Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Warns about Serious Side Effects from Maalox Product Mix-Ups, U.S. Food & Drug Administration (FDA)
• Maalox Total Relief: Medication Use Errors- Consumers with history of GI ulcers or bleeding disorder should not use product because it contains substance related to aspirin, FDA MedWatch
• Avoid Maalox Mix-Ups, U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Drug Safety Communication: Product Confusion with Maalox Total Relief and Maalox Liquid Products, U.S. Food & Drug Administration (FDA)
• Walong Marketing, Inc. Issues Nationwide Voluntary Recall of Flying Horse Black and White Sesame Chewy Candy Due to Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 17, 2010, U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Announces Animal Health Twitter Account, U.S. Food & Drug Administration (FDA)
• FDA Update on the Investigation into the Salmonella Montevideo Outbreak, U.S. Food & Drug Administration (FDA)
• Erythropoiesis-Stimulating Agents (ESAs): Requirement that only hospitals and healthcare professionals who have enrolled, completed training in risk mgmt program will prescribe, dispense ESAs to patients with cancer, FDA MedWatch
• FDA Announces New Safety Plan for Agents Used to Treat Chemotherapy-Related Anemia, U.S. Food & Drug Administration (FDA)
• Drug Information Update - Drug Safety Communication: Erythropoiesis-Stimulating Agents (ESAs): Procrit, Epogen and Aranesp, U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Company pleads guilty to felony misbranding of a drug, U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Subject sentenced to 51 months for sale of unapproved medical devices, U.S. Food & Drug Administration (FDA)
• U.S. Attorney New Release: Business Owner Pleads Guilty to Fraudulently Marketing Dietary Supplements, U.S. Food & Drug Administration (FDA)
• Nature's Variety Issues Nationwide Voluntary Recall On Raw Frozen Chicken Diets With A "Best If Used By" Date Of 11/10/10, U.S. Food & Drug Administration (FDA)
• Trader Joe's Company Voluntarily Recalls Chocolate Chip Chewy Coated Granola Bars, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Trader Joe's Company Voluntarily Recalls Chocolate Chip Chewy Coated Granola Bars, U.S. Food & Drug Administration (FDA)
• Stop & Shop Removes from Sale 24oz. Party Platter Cookies, Products Recalled Due to an Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• Estrella Family Creamery Recalls Red Darla Cheese Due to Possible Health Risks, U.S. Food & Drug Administration (FDA)
• There will be no Enforcement Report for February 10, 2010, U.S. Food & Drug Administration (FDA)
• Giant Food Recalls 24 oz. Party Platter Cookies, U.S. Food & Drug Administration (FDA)
• Cardiac Science Automated External Defibrillators (Powerheart, Cardiovive, CardioLife models): Recall- Device may not be able to deliver therapy during a cardiac resuscitation attempt, FDA MedWatch
• BD Q-Syte Luer Access Devices: Recall-Device may cause an air embolism or leakage of blood and/or therapy, which may result in serious injury or death, FDA MedWatch
• Acacia, Inc. Announces Worldwide Voluntary Recall of IV Extension Sets with BD Q-Syte[TM] Luer Access Device, U.S. Food & Drug Administration (FDA)
• FDA Approves New Indication for Crestor, U.S. Food & Drug Administration (FDA)
• FDA Unveils Initiative to Reduce Unnecessary Radiation Exposure from Medical Imaging, U.S. Food & Drug Administration (FDA)
• BD Announces Worldwide Voluntary Recall ofBD Q-Syte[TM] Luer Access Devices and BD Nexiva[TM] Closed IV Catheter Systems, U.S. Food & Drug Administration (FDA)
• Turkey Hill Dairy Issues Recall On Chocolate Marshmallow Ice Cream That May Contain Undeclared Treenuts (Almonds), U.S. Food & Drug Administration (FDA)
• Cardiac Science Notifies AED Customers of Voluntary Medical Device Recall, U.S. Food & Drug Administration (FDA)
• Drug Information Update- Questions and Answers for Healthcare Professionals: CRESTOR and the JUPITER Trial, U.S. Food & Drug Administration (FDA)
• FDA Issues Guidance to Help Streamline Medical Device Clinical Trials, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Drug Safety Communication: Risk of Progressive Multifocal Leukoencephalopathy (PML) for the use of Tysabri, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tysabri (Natalizumab): Risk of developing progressive multifocal leukoencephalopathy (PML) increases with increasing duration of exposure to Tysabri, FDA MedWatch
• Cousins Products, Llc, Issues An Allergy Alert On Undeclared Egg, Soy, And Wheat In Spinach Vinaigrette, U.S. Food & Drug Administration (FDA)
• Haifa Smoked Fish Inc. Issues An Allert On Uneviscerated Whole Schmaltz Herring, U.S. Food & Drug Administration (FDA)
• Safesheath CSG Coronary Sinus Guide Hemostatic Introducer System: Class 1 Recall -Sheath tip may break off and separate while the sheath is inside blood vessel, FDA MedWatch
• FDA Updates Statement on the Investigation into the Salmonella Montevideo Outbreak, U.S. Food & Drug Administration (FDA)
• Pierino Frozen Foods Inc. Issues an Allergy Alert on Undeclared Eggs in Its Jumbo Shells with Cheese, U.S. Food & Drug Administration (FDA)
• United States Seizes more than 1500 Cases of Food from Wisconsin Distribution Warehouse, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 3, 2010, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - February 2010 FDA Patient Safety News now available, FDA MedWatch
• FDA's MedWatch Safety Alerts: January 2010, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Approves Xiaflex for Debilitating Hand Condition, U.S. Food & Drug Administration (FDA)
• FDA Approves Xiaflex for Debilitating Hand Condition, U.S. Food & Drug Administration (FDA)
• Global Commodities Inc. Issues Allergy Alert On Undeclared Sulfites In Aahu Barah Brand Dry Apricot, U.S. Food & Drug Administration (FDA)
• FDA Requests $4.03 Billion to Transform Food Safety System, Invest in Medical Product Safety, Regulatory Science, U.S. Food & Drug Administration (FDA)
• FDA Announces Safety Risk Associated with HIV Drug, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Expands Use of Approved Breast Cancer Drug, U.S. Food & Drug Administration (FDA)
• FDA Statement on the Investigation into the Salmonella Montevideo Outbreak, U.S. Food & Drug Administration (FDA)
• FDA Expands Use of Approved Breast Cancer Drug, U.S. Food & Drug Administration (FDA)
• Zyprexa (olanzapine): Use in Adolescents - Clinicians should consider potential long-term risks when prescribing to adolescents, FDA MedWatch
• Eat for a Healthy Heart, U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Stakeholder Advisory: FDA Technical Briefing on Its FY 2011 Budget Request, U.S. Food & Drug Administration (FDA)
• Videx/Videx EC (didanosine): Labeling Revision - Risk of Non-Cirrhotic Portal Hypertension, FDA MedWatch
• United States Seizes Unapproved Ozone Generators, U.S. Food & Drug Administration (FDA)
• Drug Information Update - Serious Liver Disorder Associated with the Use of Videx/Videx EC (didanosine), U.S. Food & Drug Administration (FDA)
• Edwards Lifesciences Aquarius Hemodialysis System: Recall, U.S. Food & Drug Administration (FDA)
• Hettich Centrifuges with 2050 and 2076 Plastic Rotors: Recall, U.S. Food & Drug Administration (FDA)
• Edwards Lifesciences Aquarius Hemodialysis System: Recall - Clinically significant fluid imbalance and potential for users to repeatedly override the fluid imbalance alarm, FDA MedWatch
• Hettich Centrifuges with Plastic Rotors: Recall - Hematocrit rotor may crack, break apart and be forcefully ejected, FDA MedWatch
• Drug Information Update - FDA Issues a Draft Guidance for Industry on Assessment of Abuse Potential of Drugs, U.S. Food & Drug Administration (FDA)
• Infusion Set Needles [Manufactured by Nipro for Exelint]: Recall, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Upcoming Veterinary Medicine Advisory Committee Meeting to Discuss ProHeart® 6, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 27, 2010, U.S. Food & Drug Administration (FDA)
• Velcade (bortezomib): Starting Dose Adjustments-Patients with moderate/severe hepatic impairment should be treated with reduced starting doses, closely monitored, FDA MedWatch
• Infusion Set Needles [Manufactured by Nipro for Exelint]: Class I recall due to "coring", dislodging of silicone cores/slivers from ports into which inserted, FDA MedWatch
• FDA Announces Class I Recall of Certain Infusion Set Needles, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Announces Class I Recall of Certain Infusion Set Needles, U.S. Food & Drug Administration (FDA)
• FDA Approves Morphine Sulfate Oral Solution for Relief of Acute and Chronic Pain, U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA Approves Morphine Sulfate Oral Solution for Relief of Acute and Chronic Pain, U.S. Food & Drug Administration (FDA)
• FDA 101: Smoking Cessation Products, U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA approves Victoza (liraglutide) to treat type 2 diabetes mellitus in adults, U.S. Food & Drug Administration (FDA)
• FDA Approves New Treatment for Type 2 Diabetes, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA approves new treatment for Type 2 diabetes, U.S. Food & Drug Administration (FDA)
• FDA Approves First Percutaneous Heart Valve, U.S. Food & Drug Administration (FDA)
• Warning: Counterfeit Alli, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Approves Ampyra to Improve Walking in Adults with Multiple Sclerosis, U.S. Food & Drug Administration (FDA)
• Nipro Medical Corporation Issues a Voluntary Recall of All GlucoPro Insulin Syringes, U.S. Food & Drug Administration (FDA)
• FDA Approves Ampyra to Improve Walking in Adults with Multiple Sclerosis, U.S. Food & Drug Administration (FDA)
• Hettich Centrifuges Issues a North America and Canada Recall of Plastic Hematocrit Rotors, U.S. Food & Drug Administration (FDA)
• FDA Schedules Public Meeting on Premarket Clearance Process for Medical Devices, U.S. Food & Drug Administration (FDA)
• Drug Information Update- UPDATED Public Health Alert: Counterfeit Alli containing sibutramine, U.S. Food & Drug Administration (FDA)
• UPDATE - Alli 60 mg capsules : Counterfeit Product containing undeclared drug, sibutramine, in up to 3 times usual daily dose, FDA MedWatch
• Nipro GlucoPro Insulin Syringes: Recall - Needles may become detached and remain in the skin, FDA MedWatch
• The Wisconsin Cheeseman® Recalls Cheese Logs/Cheese Balls, U.S. Food & Drug Administration (FDA)
• Meridia (sibutramine hydrochloride): New contraindication to use in patients with history of CV disease, FDA MedWatch
• Drug Information Update- Follow-Up to the November 2009 Early Communication about an Ongoing Safety Review of Sibutramine, Marketed as Meridia, U.S. Food & Drug Administration (FDA)
• Drug Information Update- FDA Warns Consumers about Counterfeit Alli, U.S. Food & Drug Administration (FDA)
• FDA Approves Left Ventricular Assist System for Severe Heart Failure Patients, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 20, 2010, U.S. Food & Drug Administration (FDA)
• U.S. Attorney New Release: Bellevue, Washington Salon Owner Sentenced in Connection with Unlicensed Cosmetic Treatments, U.S. Food & Drug Administration (FDA)
• Alli 60 mg capsules: Counterfeit Product - sold on Internet and containing undeclared drug, sibutramine, FDA MedWatch
• FDA Warns Consumers about Counterfeit Alli, U.S. Food & Drug Administration (FDA)
• Hines Nut Company Announces Recall of Pine Nuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• PEO Chapter FO Recalls Roasted Hazelnuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• MuscleMaster.com Conducts a Voluntary Nationwide Recall of Certain Body Building Products, U.S. Food & Drug Administration (FDA)
• FDA Commissioner Addresses Nation's Health Care Professionals on H1N1 Vaccine Safety, U.S. Food & Drug Administration (FDA)
• Parkers Farm, Inc. Expands Recall to Include All of Its Products, Regardless of Code Dates, Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 13, 2010, U.S. Food & Drug Administration (FDA)
• MuscleMaster(dot)com products: Recall (Corrected link provided for previous notification), FDA MedWatch
• MuscleMaster.com products: Recall - Sold as dietary supplements but containing undeclared steroid drug product, FDA MedWatch
• FDA MedWatch - Dear Healthcare Professional Letter re: H1N1 vaccine safety from FDA Commissioner Hamburg, FDA MedWatch
• McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products in the Americas, UAE, and Fiji, U.S. Food & Drug Administration (FDA)
• McNeil Consumer Healthcare OTC products: Recall - 12/09 recall of Tylenol arthritis caplets now expanded to multiple other products, FDA MedWatch
• Drug Information Update: McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New -- FDA Basics, U.S. Food & Drug Administration (FDA)
• U.S. Attorney New Release: Anesthesiologist Charged With Falsifying Medical Research, U.S. Food & Drug Administration (FDA)
• FDA Health Alert for Merrick Beef Filet Squares Dog Treats Packaged and Distributed by Merrick Pet Care, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Health Alert for Merrick Beef Filet Squares Dog Treats Packaged and Distributed by Merrick Pet Care, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Updates Earlier Guidance on Respiratory Treatment Spiriva HandiHaler, U.S. Food & Drug Administration (FDA)
• FDA Updates Earlier Guidance on Respiratory Treatment Spiriva HandiHaler, U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Longmont, Colorado Man Arrested For Removing And Replacing Labels On Gatorade Bottles, U.S. Food & Drug Administration (FDA)
• HAPPYTOT Stage 4 and HAPPYBABY Stage 1 & Stage 2 Pouch Meals - Recall, U.S. Food & Drug Administration (FDA)
• Nurture, Inc. Issues Voluntary Recall on select HAPPYTOT Stage 4 and HAPPYBABY Stage 1 & Stage 2 Pouch Meals Due to a Packaging Defect that could cause a Possible Bacterial Contamination, U.S. Food & Drug Administration (FDA)
• FDA Issues Consumer Alert on HAPPYTOT Stage 4 and Some HAPPYBABY Stage 1 & Stage 2 Baby Foods, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Issues Consumer Alert on HAPPYTOT Stage 4 and Some HAPPYBABY Stage 1 & Stage 2 Baby Foods, U.S. Food & Drug Administration (FDA)
• HAPPYTOT and HAPPYBABY Pouch Meals - Recall due to packaging defect that could cause possible bacterial contamination, FDA MedWatch
• Heluva Good Recalls Cold Pack Cheese Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Launches "FDA Basics" Online to Enhance Public Understanding of the Agency, U.S. Food & Drug Administration (FDA)
• FDA's MedWatch Safety Alerts: December 2009, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Unveils First Phase of Transparency Initiative, U.S. Food & Drug Administration (FDA)
• FDA Unveils First Phase of Transparency Initiative, U.S. Food & Drug Administration (FDA)
• Drug Information Update: FDA Approves New Drug for Rheumatoid Arthritis, U.S. Food & Drug Administration (FDA)
• Rudolph Foods Issues Allergy Alert on Undeclared Milk in Product, U.S. Food & Drug Administration (FDA)
• PARKERS FARM, INC. RECALLS SEVERAL PRODUCTS BECAUSE OF POSSIBLE HEALTH RISK, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Parkers Farm, Inc. Recalls Several Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - December 2009 Drug Safety Labeling Changes: 28 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• Rapamune (sirolimus): Drug Monitoring Recommendations-Switching between assays for the same patient can produce differing results that may be clinically significant, FDA MedWatch
• FDA Approves New Drug for Rheumatoid Arthritis, U.S. Food & Drug Administration (FDA)
• FDA Requires Sybaritic, Inc. to Stop Producing Unapproved Medical Devices, U.S. Food & Drug Administration (FDA)
• FDA Awards Contract to Harvard Pilgrim to Develop Pilot for Safety Monitoring System, U.S. Food & Drug Administration (FDA)
• FDA Ends Maryland Seafood Processor's Pattern of Sanitary Violations, U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Announces the Availability of the 4th Edition of the Animal Feed Safety System Framework Document, U.S. Food & Drug Administration (FDA)
• Bao Ding Seafood Recalls Boiled Horse Mackerel, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - January 2010 FDA Patient Safety News now available, FDA MedWatch
• FDA Seizes More Than $1 Million Worth of Food from Nashville Food Processor and Warehouse: Agency acts to prevent distribution of food from rodent-infested facility, U.S. Food & Drug Administration (FDA)
• ev3 Endovascular Inc. Trailblazer Support Catheter: Class I Recall, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 6, 2010, U.S. Food & Drug Administration (FDA)
• Harry London Candies, Inc. announces a voluntary and limited recall of Harry London Chocolate Pecan Caramel Stars due to an undeclared allergen, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - ev3 Endovascular Inc. Trailblazer Support Catheter: Device may crack near the radiopaque marker band, potentially resulting in serious patient injury, FDA MedWatch
• FDA Takes Action Against New Jersey Cheese Manufacturer, U.S. Food & Drug Administration (FDA)
• Nutty Guys Issues Public Notice on Voluntary Recall of Butter Toffee Peanuts and Yogurt Covered Peanuts, U.S. Food & Drug Administration (FDA)
• Nzu, Traditional Remedy for Morning Sickness:Women advised to avoid because of potential health risks from high levels of lead and arsenic, FDA MedWatch
• Publix Issues Allergy Alert on Pecans in Publix Pumpkin Pecan Streusel Pie, U.S. Food & Drug Administration (FDA)
• Drug Information Update - FDA, Health Organizations to Study Safety of Medications Taken During Pregnancy, U.S. Food & Drug Administration (FDA)
• FDA, Health Organizations to Study Safety of Medications Taken During Pregnancy, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 30, 2009, U.S. Food & Drug Administration (FDA)
• Janzen Farms Recalls Hazelnut Kernels Because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• U.S. Attorney News Release: Colorado-Based Spectranetics Corporation to Pay $5 Million to Resolve Allegations Relating to Its Medical Devices, U.S. Food & Drug Administration (FDA)
• FDA Warns Public of Continued Extortion Scam by FDA Impersonators, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA warns public of continued extortion scam by FDA impersonators, U.S. Food & Drug Administration (FDA)
• Tylenol Arthritis Pain Caplet 100 count: Recall of all lots due to reports of odor associated with nausea, vomiting and diarrhea, FDA MedWatch
• Mcneil Consumer Healthcare Announces A Voluntary Nationwide Recall Of All Lots Of Tylenol® Arthritis Pain 100 Count With Ez-Open Cap, U.S. Food & Drug Administration (FDA)
• Encompass Group Voluntarily Recalls Thermoflect Product Line, U.S. Food & Drug Administration (FDA)
• Thermoflect Blankets and product line - Recall: Products are not to be used in MR environment, FDA MedWatch
• Mountain Man Nut & Fruit Co.® Announces Voluntary Recall of Hazelnut, U.S. Food & Drug Administration (FDA)
• Market of Choice Recalls Hazelnuts Because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• FDA Approves A High Dose Seasonal Influenza Vaccine Specifically Intended for People Ages 65 and Older, U.S. Food & Drug Administration (FDA)
• FDA: Orphan Drug Workshops Scheduled For Feb. 25-26 and Aug. 3-4, 2010, U.S. Food & Drug Administration (FDA)
• Burnt Ridge Orchards, Inc. Recalls Shelled Hazelnuts Because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• Drug Information Update: Follow-Up to the August 2008 Early Communication About an Ongoing Safety Review of Ezetimibe/Simvastatin, Simvastatin and Ezetimibe, U.S. Food & Drug Administration (FDA)
• Health Fraud Awareness (video), U.S. Food & Drug Administration (FDA)
• Teva Animal Health, Inc. expands a voluntary nationwide recall of Ketamine Hydrochloride Injection, USP CIII 100mg/mL in 10mL vials, U.S. Food & Drug Administration (FDA)
• Whole Foods Market® Recalls Bulk Hazelnuts, U.S. Food & Drug Administration (FDA)
• Harry and David Conducts Hazelnut Recall in Medford, Oregon because of Possible Risk to Health, U.S. Food & Drug Administration (FDA)
• Evonuk Oregon Hazelnuts Recalls Raw and Dry Roasted Hazelnut Kernels Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kunze Farms Recalls Hazelnut Kernels because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 16, 2009, U.S. Food & Drug Administration (FDA)
• Willamette Shelling Recalls Shelled Hazelnuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Willamette Filbert Growers Recalls Shelled Hazelnuts and Shelled Organic Hazelnus Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Faribault Foods Voluntarily Recalls Three Lots of Health Valley Organic No Salt Added Split Pea Soup Due to the Presence of an Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• Cleviprex (clevidipine butyrate): Recall of injectable emulsion due to presence of particulate matter, FDA MedWatch
• The Medicines Company Issues a Nationwide Recall for Certain Lots of Cleviprex® That May Contain Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - November 2009 Drug Safety Labeling Changes: 44 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• FDA Approves Generic Aricept to Treat Dementia Related to Alzheimer's Disease, U.S. Food & Drug Administration (FDA)
• Atlas Operations: Recall of Sexual Enhancement Products - Undeclared drug, sulfoaildenafil, may result in lowering blood pressure to dangerous levels, FDA MedWatch
• Drug Information Update- FDA Approves First Generic Aricept to Treat Dementia Related to Alzheimer's Disease, U.S. Food & Drug Administration (FDA)
• FDA Approves First Generic Aricept to Treat Dementia Related to Alzheimer's Disease, U.S. Food & Drug Administration (FDA)
• FDA Expands Presence Outside U.S. with Opening of Mexico City Post, U.S. Food & Drug Administration (FDA)
• Simple Foods, Inc. - Undeclared allergen (milk), U.S. Food & Drug Administration (FDA)
• Atlas Operations, Inc. Issues a Nationwide Voluntary Recall of Specific Lots of Sexual Enhancement Products Marketed as Dietary Supplements, U.S. Food & Drug Administration (FDA)
• Drug Information Update - Public Health Advisory: Availability of Tamiflu for Oral Suspension, U.S. Food & Drug Administration (FDA)
• Limited Recall of 120 Cartons of Berries & Balsamic Salad due to Unlabeled Allergen, U.S. Food & Drug Administration (FDA)
• FDA Debars Convicted Virginia Seafood Dealer from Importing Food for 20 Years, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Notice of Pilot Project of Electronic Margin of Safety and Submission of NonClinical Toxicology Study Data, U.S. Food & Drug Administration (FDA)
• Pet Carousel Conducts Nationwide Recall of Beef Hoof Products and Pig Ears Because of Salmonella Risk, U.S. Food & Drug Administration (FDA)
• Negative Pressure Wound Devices Draw FDA Notice, Advice, U.S. Food & Drug Administration (FDA)
• Stryker Operating Room System II Surgical Navigation System - Recall, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 9, 2009, U.S. Food & Drug Administration (FDA)
• Drug Information Update - Final Regulation on Positron Emission Tomography (PET) Drugs, U.S. Food & Drug Administration (FDA)
• USDA and HHS Continue Food Safety Working Group Efforts; Customs and Border Protection Opens Import Food Safety Center, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Alka-Seltzer Plus Day & Night Cold Formula Liquid Gels - Incorrect Packaging, FDA MedWatch
• Bayer Consumer Care Voluntarily Recalls One Lot of Combination Package of Alka-Seltzer Plus® Day & Night Cold Formula Liquid Gels, U.S. Food & Drug Administration (FDA)
• Rock Creek Nut Company Issues Allergy Alert on Undeclared Milk And Soy in "Quick Fix" Trail Mix, U.S. Food & Drug Administration (FDA)