FDA News Releases

• Date Index

• Pedigree Brand wet dog food recalled, FoodSafety.gov
• HIV/AIDS Update - Tentative approval of lopinavir and ritonavir Oral Solution, 80 mg/20 mg per mL, U.S. Food & Drug Administration (FDA)
• Standard Process Recall: Three Supplements Because of Possible Health Risk, FoodSafety.gov
• Banner Mountain Sprouts Voluntarily Recalls Organic Sprouts, FoodSafety.gov
• Dole Fresh Vegetables Recall: Salads, FoodSafety.gov
• Healthy Choice Recall: All Sizes of Liquid Gold Carrot Juice Because of Possible Health Risk, FoodSafety.gov
• RECALL: approximately 1,350 pounds of a ground smoked bacon product, FoodSafety.gov
• Recall Leasa Living Alfalfa Sprouts: Possible Health Risk, FoodSafety.gov
• Mars Petcare US Announces Voluntary Recall of Limited Range of Pedigree ® Brand Wet Dog Food, U.S. Food & Drug Administration (FDA)
• ITO EN Asks Hawaii Customers of Aloha Maid Coconut Water with Pineapple to Return Product to Store, U.S. Food & Drug Administration (FDA)
• The July 2012 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Mars Petcare US Announces Voluntary Recall of Limited Range of Pedigree® Brand Wet Dog Food, U.S. Food & Drug Administration (FDA)
• Listeria Contamination in Queso Fresco, Fresh Cheese, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Listeria Contamination in Queso Fresco, Fresh Cheese, FoodSafety.gov
• Dole Fresh Vegetables Announces Precautionary Recall of Limited Number of Salads_, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cataplex ACP, Cataplex C, and Pancreatrophin PMG Dietary Supplements: Recall - Potential for Contamination With Salmonella, FDA MedWatch
• Standard Process Issues Voluntary Recall of Three Supplements Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• The Affordable Care Act Is Moving Forward, HealthCare.gov
• FDA MedWatch - Ondansetron (Zofran) IV: Drug Safety Communication - QT Prolongation, FDA MedWatch
• FDA MedWatch - Vecuronium Bromide For Injection Preservative Free (Bedford Laboratories): Recall - Particulate Matter, FDA MedWatch
• FDA MedWatch - ev3 Onyx Liquid Embolic System: Safety Communication - Risk of Catheter Entrapment, FDA MedWatch
• Bedford Laboratories Issues Voluntary Hospital/User-Level Recall Of Vecuronium Bromide For Injection Preservative Free, Lot 2067134, Because Of Health Risk, U.S. Food & Drug Administration (FDA)
• Healthy Choice Recalls All Sizes of Liquid Gold Carrot Juice for Possible Health Risk, FoodSafety.gov
• FDA approves Myrbetriq for overactive bladder, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 27, 2012, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Enforcement Report for June 27, 2012, U.S. Food & Drug Administration (FDA)
  • Enforcement Report for June 27, 2012, U.S. Food & Drug Administration (FDA)
• FDA approves Belviq to treat some overweight or obese adults, U.S. Food & Drug Administration (FDA)
• Banner Mountain Sprouts Voluntarily Recalls Organic Sprouts Because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Incivek (telaprevir) product labeling revised, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tenative approval for efavirenz tablets, 600 mg for PEPFAR, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cefepime:Label Change- Risk of Seizure in Patients Not Receiving Dosage Adjustments for Kidney Impairment, FDA MedWatch
• FDA Minority Health Webinar available online, U.S. Food & Drug Administration (FDA)
• Dole Fresh Vegetables Announces Precautionary Recall of Limited Number of Salads, June 22, 2012, U.S. Food & Drug Administration (FDA)
• Healthy Choice Recalls All Sizes of Liquid Gold Carrot Juice Including 128oz, 64oz, 32oz, and 16oz Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tenative approval of efavirenz tablets, 600 mg, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Implements Simpler Process for Feed Mill Registration, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nidek Medical Products Mark 5 Nuvo, Nuvo 8, and Nuvo Lite Oxygen Concentrators: Class I Recall - Risk of Fire, Loss of Supplemental Oxygen, FDA MedWatch
• Leasa Industries Co., Inc. Recalls Leasa Brand 6 oz Living Alfalfa Sprouts Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Drug Approved to Help Agriculture's Helpful Honey Bees, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 20, 2012, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Enforcement Report for June 20, 2012, U.S. Food & Drug Administration (FDA)
  • Enforcement Report for June 20, 2012, U.S. Food & Drug Administration (FDA)
• Health Care Law Expands Community Health Centers, Serves More Patients, HealthCare.gov
• Update of CVM's What's New - ADUFA III Negotiation Meeting Minutes, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of generic abacavir tablets, 300 mg, U.S. Food & Drug Administration (FDA)
• Euphoria Fancy Food Inc Issues an Alert on Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• Nidek Medical Products, Inc. issues an Urgent Medical Device Correction affecting oxygen concentrators, U.S. Food & Drug Administration (FDA)
• ALERT: Hannaford Mini Frosted Cookies: Egg Ingredient Warning, FoodSafety.gov
• Update of CVM's What's New - Draft Guidance for Industry Available, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Draft Guidance for Industry Available, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Draft Guidance for Industry Available, U.S. Food & Drug Administration (FDA)
• Hannaford Mini Frosted Cookies: Egg Ingredient Warning, U.S. Food & Drug Administration (FDA)
• ALERT: Undeclared Soy In 15 Oz Premium Navy Beans, FoodSafety.gov
• Update of CVM's What's New - Updated Index of Legally Marketed Unapproved New Animal Drugs for Minor Species, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Index of Legally Marketed Unapproved New Animal Drugs for Minor Species, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Index of Legally Marketed Unapproved New Animal Drugs for Minor Species, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Index of Legally Marketed Unapproved New Animal Drugs for Minor Species, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update -Tentative approval Lamivudine / Zidovudine Fixed Dose Combination for pediatric use, U.S. Food & Drug Administration (FDA)
• Truitt Bros., Inc. Issues Allergy Alert On Undeclared Soy In 15 Oz Premium Navy Beans, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - SIGMA Spectrum Infusion Pump - Expanded Class I Recall issued. Risk of over-infusion, could result in serious injury or death., FDA MedWatch
• RECALL: Raw Stuffed Chicken Product, FoodSafety.gov
• Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Veterinary Master Files, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 13, 2012, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Paper Trail Publications Database Available, U.S. Food & Drug Administration (FDA)
• ALERT: Pints Of Ben & Jerry's Chocolate Ice Cream, FoodSafety.gov
• RECALL: Red Pepper Onion & Garlic Cheddar, FoodSafety.gov
• Unilever Issues Allergy Alert On Pints Of Ben & Jerry's Chocolate Nougat Crunch Ice Cream:Sweet Cream Ice Cream with Fudge Covered Wafer Cookies & a Chocolate Nougat Swirl, U.S. Food & Drug Administration (FDA)
• Golden Glen Creamery Issues Voluntary Recall Of Red Pepper Onion & Garlic Cheddar Because Of Potential Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - May 2012 Safety Labeling Changes includes 41 products with revisions to Prescribing Information, FDA MedWatch
• RECALL: 55,757 pounds of pork dumplings contain MSG, FoodSafety.gov
• Update of CVM's What's New - June 2012 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• ALERT: Undeclared Walnut In Best Maid Cookie, FoodSafety.gov
• FDA approves Perjeta for type of late-stage breast cancer, U.S. Food & Drug Administration (FDA)
• Join Us for a Seniors Health Town Hall @ 10 a.m., HealthCare.gov
• Best Maid Cookie Company Issues Allergy Alert On Undeclared Walnut In Product, U.S. Food & Drug Administration (FDA)
• RECALL: Meat Lasagna Products Due to Misbranding and Undeclared Allergens, FoodSafety.gov
• RECALL: Digestive 3 in 1 Health' Because of Possible Health Risk, FoodSafety.gov
• FDA MedWatch - Digestive 3 in 1 Health Liquid Dietary Supplement: Recall - Potential for Contamination With Salmonella, FDA MedWatch
• Voluntary Recall Of Pasta Mix Products, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Voluntary Recall Of Pasta Mix Products, FoodSafety.gov
• Enforcement Report for June 6, 2012, U.S. Food & Drug Administration (FDA)
• Join Us for a Women’s Health Town Hall, HealthCare.gov
• Botanical Laboratories Inc. Recalls Wellesse Digestive 3 in 1 Health® Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - New page on the FDA.gov site - Development of Topical Microbicides, U.S. Food & Drug Administration (FDA)
• Sandoz US Announces Precautionary Recall Of Oral Contraceptive Introvale®, Following Report Of Packaging Flaw, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Introvale (levonorgestrel and ethinyl estradiol) Tablets: Recall - Packaging Flaw, FDA MedWatch
• CVM Updates - FDA Announces Request for Applications for Vet-LRN Program Cooperative Agreement, U.S. Food & Drug Administration (FDA)
• U.S. Marshals seized misbranded drugs in Maine, U.S. Food & Drug Administration (FDA)
• RECALL: Pork Product for Possible Listeria Contamination, FoodSafety.gov
• Chicago Firm Recalls Pork Roll Products Due To Misbranding and Undeclared Allergen, FoodSafety.gov
• HIV/AIDS Update -Prezista (darunavir) label update, U.S. Food & Drug Administration (FDA)
• An Updated Message to our Customers - Recall of South Korea Shellfish, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • An Updated Message to our Customers - Recall of South Korea Shellfish, FoodSafety.gov
• FDA MedWatch - Reumofan Plus: Recall - Undeclared Drug Ingredient, FDA MedWatch
  • <Possible follow-ups>
  • FDA MedWatch - Reumofan Plus: Recall - Undeclared Drug Ingredient, FDA MedWatch
• HIV/AIDS Update - Two tentative approvals of lamivudine for PEPFAR, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - MOOG Medical Devices Group, Curlin Infusion Administration Sets: Class I Recall - Potential for Reverse Flow of Fluid, FDA MedWatch
• The June 2012 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 30, 2012, U.S. Food & Drug Administration (FDA)
• OSKRI CORP. ISSUES ALLERGY ALERT on UNDECLARED CASHEWS in “PEACH GRANOLA”, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • OSKRI CORP. ISSUES ALLERGY ALERT on UNDECLARED CASHEWS in “PEACH GRANOLA”, FoodSafety.gov
• Update of CVM's What's New - Updated - Investigation of Multistate Outbreak of Human Salmonella Infantis Infections Linked to Dry Dog Food, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Teva’s Adderall 30 mg Tablets: Counterfeit Product - Contains Wrong Active Ingredients, FDA MedWatch
• FDA warns consumers about counterfeit version of Teva’s Adderall, U.S. Food & Drug Administration (FDA)
• The Menz Club, LLC . Issues a voluntary nationwide recall of V-Maxx Rx due to undeclared sulfoaildenafil, U.S. Food & Drug Administration (FDA)
• RECALL: Nitre Power 4oz Plastic Bags Because of Possible Health Risks, FoodSafety.gov
• RECALL: Shiitake Slices Because Of Possible Health Risk, FoodSafety.gov
• Hocean Inc. Recalls Nitre Power 4oz Plastic Bags Because of Possible Health Risks, U.S. Food & Drug Administration (FDA)
• L.A. Link (Huntington Beach) Corporation Recalls Shiitake-Ya Brand Gourmet Shiitake Slices Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Baxa Corporation Abacus Total Parenteral Nutrition (TPN) Calculation Software: Class I Recall - Potential Dosing Errors, FDA MedWatch
• CVM Updates - Industry Reminder: Labeling of Ethoxyquin in Animal Feed, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Availability of the NARMS Strategic Plan 2012-2016, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Dialysate Concentrates Used in Hemodialysis: Safety Communication - Alkali Dosing Errors, FDA MedWatch
• RECALL: Smoked Bratwurst Due To Undeclared Allergen, FoodSafety.gov
• RECALL: Chicken Breast Due To Undeclared Allergen, FoodSafety.gov
• HIV/AIDS Update Tentative approval of lopinavir and ritonavir tablets 200 mg/50 mg, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of generic nevirapine formulations, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Franck’s Compounding Pharmacy Sterile Preparations: Reports of Fungal Endophthalmitis, Expanded Recall, FDA MedWatch
• Making Health Insurance More Affordable for Small Businesses, HealthCare.gov
• Update of CVM's What's New - Urgent: Compounded Prescription Recall, U.S. Food & Drug Administration (FDA)
• Urgent: Compounded Prescription Recall, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 23, 2012, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Generic approval of lamivudine and zidovudine tablets USP, 150 mg/300 mg, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of generic formulation of lamivudine and zidovudine Tablets, 150 mg/300 mg, U.S. Food & Drug Administration (FDA)
• Honeyville Honey Farm Issues Allergy Alert on Undeclared Anchovy in Honeyville Honey Barbecue Sauce, U.S. Food & Drug Administration (FDA)
• RECALL: Processed Salads Due to Potential Listeria, FoodSafety.gov
• RECALL: Diamond Naturals Small Breed Adult Dog Lamb & Rice Formula, FoodSafety.gov
• RECALL: Lasagna Product Due to Undeclared Allergen, FoodSafety.gov
• RECALL: Organic Baby Spinach Because Of Possible Salmonella, FoodSafety.gov
• RECALL: "Tempeh Starter Yeast" Due to Potential Salmonella, FoodSafety.gov
• RECALL: Harris Teeter Recalls Sorbet Due to Undeclared Allergen, FoodSafety.gov
• ALERT: Undeclared Anchovy in Honey Barbecue Sauce, FoodSafety.gov
• HIV/AIDS Update - Abacavir induces loading of novel self-peptides into HLA-BM57:01: an autoimmune model for HLA-associated drug hypersensitivity, U.S. Food & Drug Administration (FDA)
• Moog Medical Devices Group Announces Voluntary Recall Of Select Curlin Administration Sets Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Minutes of Meeting Available; Industry Discussions on AGDUFA II Reauthorization, U.S. Food & Drug Administration (FDA)
• Harris Teeter is Recalling 5 Flavors of Sorbet Due to Possible Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• IndonesianFoodMart.com Recalls "Tempeh Starter Yeast" because of Health Risk of Salmonell, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - CORRECTION - Hospira Carpuject Pre-filled Cartridges - Drug Alert: Products May Contain More Than the Intended Fill Volume, FDA MedWatch
• FDA MedWatch - Hopsira Carpuject Pre-filled Cartridges - Drug Alert: Products May Contain More Than the Intended Fill Volume, FDA MedWatch
• Salinas Firm Initiates A Voluntary Recall Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Focusing on Fighting Cancer, Without Fear of Lifetime Insurance Caps, HealthCare.gov
• Pacific Coast Fruit Company Recalls Single Side Serving Processed Salads for Potential Listeria monocytogenes Contamination, U.S. Food & Drug Administration (FDA)
• UPDATED: CORRECTED BEST BEFORE DATE Diamond Pet Foods Expands Voluntary Recall Diamond Naturals Small Breed Adult Dog Lamb & Rice Formula Dry Dog Food Production Code DSL 0801 Due to Small Potential for Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA-led research team discovers an autoimmune mechanism for serious drug-induced adverse reactions, U.S. Food & Drug Administration (FDA)
• Diamond Pet Foods Expands Voluntary Recall Diamond Naturals Small Breed Adult Dog Lamb & Rice Formula Dry Dog Food Production Code DSL 0801 Due to Small Potential for Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Salmonella Outbreak Associated with Raw Scraped Ground Tuna, FoodSafety.gov
• RECALL: Diced Red Onions Because of Possible Health Risk, FoodSafety.gov
• RECALL: Steakhouse Burgers Due to Undeclared Allergens, FoodSafety.gov
• RECALL: Papaya Maradol Because Of Possible Health Risk, FoodSafety.gov
• RECALL: Santos Brands Products for Undeclared Peanuts and Wheat, FoodSafety.gov
• RECALL: Turkey Burger Product Due To Undeclared Allergen, FoodSafety.gov
• RECALL: Salads Because Of Possible Health Risk, FoodSafety.gov
• River Ranch Expands Salad Recall Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Gills Onions Voluntarily Recalls One Lot of Diced Red Onions Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Caribe Produce, LTD CO. Recalls Papaya Maradol, Caribena Brand Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Santos Agency, Inc. voluntarily recalls Santos Brands Products for undeclared peanuts and wheat in California, U.S. Food & Drug Administration (FDA)
• River Ranch Recalls Retail And Food Service Salads Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• WEST COAST NUTRITIONALS, LTD. Issues a Voluntary Worldwide/Nationwide Drug Recall of Products FIRMINITE, EXTRA STRENGTH INSTANT HOT ROD, AND LIBIDRON due to Undeclared Tadalafil, U.S. Food & Drug Administration (FDA)
• RECALL: Beef Products Due To Lack of Federal Inspection, FoodSafety.gov
• RECALL: Lamb Koftis Due to Undeclared Allergen, FoodSafety.gov
• Enforcement Report for May 16, 2012, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Zithromax (azithromycin): FDA Statement on risk of cardiovascular death, FDA MedWatch
• FDA approves generic versions of blood thinner Plavix, U.S. Food & Drug Administration (FDA)
• ALERT: Undeclared Eggs in Rainbow Cake, FoodSafety.gov
• RECALL: Halal Beef Samosas, FoodSafety.gov
• Bakery El Monte Sinai Corp Announces Allergy Alert on Undeclared Eggs in Rainbow Cake, U.S. Food & Drug Administration (FDA)
• Upcoming FDA Webinar on Health Disparities, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Diamond Pet Food Processors Inspectional Observations, U.S. Food & Drug Administration (FDA)
• Free Healthy Women's Action Kit Featured in Dear Abby, U.S. Food & Drug Administration (FDA)
• RECALL: Animal Feed Products, FoodSafety.gov
• FDA MedWatch - Monthly Safety Labeling Changes includes 43 products with revisions to Prescribing Information, FDA MedWatch
• RECALL: Purina Cat Food Due to A Low Level of Thiamine (Vitamin B1), FoodSafety.gov
• FDA MedWatch - Hydromorphone Hydrochloride Injection 1 MG/ML, (C-II) 1 ML Fill In 2.5 ML Carpuject: Recall - May Contain More Than the Intended Fill Volume, FDA MedWatch
• ALERT: Undeclared Allergens In Several Jonlly Fruits Products, FoodSafety.gov
• RECALL: Undeclared Walnuts in Carrot Cake Cupcakes, FoodSafety.gov
• Celebrate National Women's Health Week, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Recalls, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Recalls, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Recalls, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Recalls, U.S. Food & Drug Administration (FDA)
• Hospira Announces A Nationwide Voluntary Recall Of One Lot Of Hydromorphone Hydrochloride Injection 1 MG/ML, (C-II) 1 ML Fill In 2.5 ML Carpuject, That May Contain More Than The Intended Fill Volume, U.S. Food & Drug Administration (FDA)
• Correction to Date Code in Natural Balance Pet Foods’ Voluntary Recall Dated May 4, 2012 Due to the Potential for Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Nestlé Purina Voluntarily Recalls Single Lot of Therapeutic Canned Cat Food Due to A Low Level of Thiamine (Vitamin B1), U.S. Food & Drug Administration (FDA)
• Whole Foods Market recalls carrot cake cupcakes for undeclared walnuts in Northern California, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of nevirapine tablets 200 mg, U.S. Food & Drug Administration (FDA)
• Jonlly Fruits Inc. Alerta De Alergia Por No Decrarar Alergenos En El Producto, U.S. Food & Drug Administration (FDA)
• Jonlly Fruits Inc. Issues Allergy Alert On Undeclared Allergens In Several Products, U.S. Food & Drug Administration (FDA)
• RECALL: Chorizo Product Due To Misbranding, FoodSafety.gov
• FDA issues alert on potential dangers of unproven treatment for multiple sclerosis, U.S. Food & Drug Administration (FDA)
• RECALL: "Tuna Strips" Product Of India "AA" Or "AAA", FoodSafety.gov
• Enforcement Report for May 9, 2012, U.S. Food & Drug Administration (FDA)
• Moon Fishery (India) Pvt. Ltd. Recalls Its "Tuna Strips" Product Of India "AA" Or "AAA" Grade Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL: Alfalfa Sprouts May be Contaminated with Listeria, FoodSafety.gov
• RECALL: Dog Food Because of Possible Salmonella Health Risk, FoodSafety.gov
• Update of CVM's What's New - Solid Gold Health Products for Pets, Inc. Recalls Dog Food Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Solid Gold Health Products for Pets, Inc. Recalls Dog Food Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Cleveland Beansprouts Co. of Cleveland, OH is recalling all alfalfa sprouts because they may be contaminated with Listeria monocytogenes, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• Water Pik, Inc. Announces Product Exchange Program, U.S. Food & Drug Administration (FDA)
• RECALL: Pet Food Due to the Potential for Salmonella, FoodSafety.gov
• RECALL: Dry Pet Food Due to the Potential for Salmonella, FoodSafety.gov
• Update of CVM's What's New - Apex Pet Foods Initiates Voluntary Recall of Dry Pet Food Due to the Potential for Salmonella, U.S. Food & Drug Administration (FDA)
• Apex Pet Foods Initiates Voluntary Recall of Dry Pet Food Due to the Potential for Salmonella No Pet or Human Illnesses have been Reported Associated With Apex Dog Food, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Pet Food Recalls, U.S. Food & Drug Administration (FDA)
• RECALL: Dry Dog Food Due To Possible Salmonella, FoodSafety.gov
• RECALL UPDATE: Diamond Pet Foods Production Code Information, FoodSafety.gov
• UPDATED: CORRECT PRODUCTION CODE INFORMATION Diamond Pet Foods Expands Voluntary Recall of Dry Pet Food Due to Potential Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• UPDATED: CORRECT PRODUCTION CODE INFORMATION Canidae Pet Foods Initiates Voluntary Recall of Dry Pet Food Due to the Potential for Salmonella, U.S. Food & Drug Administration (FDA)
• Natural Balance Pet Foods Initiates Voluntary Recall of Certain Dry Pet Food Due to the Potential for Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Wellpet LLC Voluntarily Recalls One Recipe Of Dry Dog Food Due To Salmonella At Diamond Pet Foods' Facility, U.S. Food & Drug Administration (FDA)
• Upcoming Advisory Committee Meeting, U.S. Food & Drug Administration (FDA)
• RECALL: World Berries™ Because of Possible E. Coli, FoodSafety.gov
• Funfresh Foods, Inc. Voluntarily Recalls World Berries™ Organic “Cacao Nibs” Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Franck's Compounding Pharmacy - Ongoing Investigation of Fungal Endophthalmitis Cases, FDA MedWatch
• RECALL: Asian Ready-to-Eat Meals due to Possible Health Risk, FoodSafety.gov
• ALERT: Undeclared Almonds In Lemon Bar Bliss, FoodSafety.gov
• Providing Preventive Services to Patients in Community Health Centers, HealthCare.gov
• Update of CVM's What's New - Investigation of a Multi-state Outbreak of Salmonella Infantis Linked to Dry Dog Food, U.S. Food & Drug Administration (FDA)
• Church & Dwight Co., Inc. Voluntarily Recalls Select Lots of Spinbrush® Rechargeable SONIC Toothbrushes Distributed Between February 2010 and October 2011 for Possible Health Risk, U.S. Food & Drug Administration (FDA)
• H-E-B Issues a Precautionary Recall For Asian Ready-to-Eat Meals due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FIGI’S INC. Issues Allergy Alert On Undeclared Almonds In Lemon Bar Bliss, U.S. Food & Drug Administration (FDA)
• Notice of Recall - Triamcinolone acetonide P.F. 80mg/ml, U.S. Food & Drug Administration (FDA)
• FDA issues final rule on sterility testing of biological products, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 2, 2012, U.S. Food & Drug Administration (FDA)
• RECALL: Puppy Formula due to Possible Salmonella Contamination, FoodSafety.gov
• RECALL: Forti-Diet Pro Health Mouse, Rat and Hamster, FoodSafety.gov
• RECALL: Tempeh because of Possible Health Risk, FoodSafety.gov
• RECALL: Soybean Sprouts Due To Possible Listeria, FoodSafety.gov
• Update of CVM's What's New - Updated Questions and Answers Regarding Chicken Jerky Treats from China, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Questions and Answers Regarding Chicken Jerky Treats from China, U.S. Food & Drug Administration (FDA)
• Henry's Farm Inc. Expands Recall Of Soybean Sprouts Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves new orphan drug to treat a form of Gaucher disease, U.S. Food & Drug Administration (FDA)
• Smiling Hara Recalls Tempeh because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Asheville Company Recalls Tempeh After Tests Detect Presence Of Salmonella, U.S. Food & Drug Administration (FDA)
• The May 2012 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Kaytee Recalls Forti-Diet Pro Health Mouse, Rat and Hamster, U.S. Food & Drug Administration (FDA)
• Kaytee Recalls Forti-Diet Pro Health Mouse, Rat and Hamster Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Diamond Pet Foods Expands Voluntary Recall to Include Diamond Puppy Formula, U.S. Food & Drug Administration (FDA)
• Diamond Pet Foods Expands Voluntary Recall to Include Diamond Puppy Formula due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of nevirapine Tablets for Oral Suspension, 50 mg and 100 mg for pediatric use, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - New pediatric Lexiva dosing regimen for patients from at least 4 weeks to less than 6 years of age, U.S. Food & Drug Administration (FDA)
• Limited Recall Of DuMOR Poultry Grower/Finisher Bags Containing DuMOR Poultry Layer 16% Crumbles Because of Possible Animal Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Minutes of Meeting Available; Industry Discussions on ADUFA III Reauthorization, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Minutes of Meeting Available; Industry Discussions on ADUFA III Reauthorization, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Diamond Pet Foods Expands Voluntary Recall, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Diamond Pet Foods Expands Voluntary Recall, U.S. Food & Drug Administration (FDA)
• RECALL: Incorrectly Packaged Feed, FoodSafety.gov
• RECALL: Diamond Pet Foods Dry Dog Food Tests Positive For Salmonella, FoodSafety.gov
• Diamond Pet Foods Expands Voluntary Recall of One Production Run of Dry Dog Food Due to a Potential Health Risk Recall is limited to one formula of Chicken Soup for the Pet Lover’s Soul distributed to 10 states, U.S. Food & Drug Administration (FDA)
• FDA approves Stendra for erectile dysfunction, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Recall, U.S. Food & Drug Administration (FDA)
• Limited Recall Of DuMOR® Poultry Grower/Finisher Bags Containing DuMOR® Poultry Layer 16% Crumbles Because of Possible Animal Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL: Alfalfa and Clover Sprouts Due To Possible Listeria, FoodSafety.gov
• ALERT: Undeclared Milk in Dark Chocolate Bar, FoodSafety.gov
• ALERT: Undeclared Sulfites In Shad Javantri (Whole Mace), FoodSafety.gov
• Alfa Sprouts Inc. (Springwater Sprouts) Recalls Alfalfa Sprouts And Clover Sprouts Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Fatima Brothers Issues An Allert On Undeclared Sulfites In Shad Javantri (Whole Mace), U.S. Food & Drug Administration (FDA)
• Allergy Alert on Milk Products in Mrs. Weaver's Pimento Spread, U.S. Food & Drug Administration (FDA)
• Café-Tasse Issues Allergy Alert on Undeclared Milk in Café-Tasse 45 gr. Noir (Dark) Chocolate Bar., U.S. Food & Drug Administration (FDA)
• FDA approves Votrient for advanced soft tissue sarcoma, U.S. Food & Drug Administration (FDA)
• FDA approves Afinitor for non-cancerous kidney tumors caused by rare genetic disease, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Statement on USDA Announcement of Positive BSE Test Result, U.S. Food & Drug Administration (FDA)
• ALERT: Milk Products in Pimento Spread, FoodSafety.gov
• RECALL: Undeclared Milk, Wheat and Egg in Candy Mix, FoodSafety.gov
• Enforcement Report for April 25, 2012, U.S. Food & Drug Administration (FDA)
• LA STAR SEAFOOD CO, INC. RECALLS DRY and SMOKED VOBLA FISH BECAUSE of POSSIBLE HEALTH RISK, U.S. Food & Drug Administration (FDA)
• KRISPAK INC. ISSUES RECALL DUE TO MIS-PACK, RESULTING in POTENTIAL ALLERGY ALERT on UNDECLARED MILK, WHEAT, and EGG in GFS BRAND HOSTESS CANDY MIX, U.S. Food & Drug Administration (FDA)
• Allergy Alert on Milk Products in Mrs. Weaver’s Pimento Spread, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Epinephrine Injection, USP, 1:1000, 1mL Ampules Lot #1395 Due to Discoloration and Small Visible Particles, U.S. Food & Drug Administration (FDA)
• Coverage for Children with Pre-Existing Conditions - Tracy's Story, HealthCare.gov
• Update of CVM's What's New - Potassium Bromide: Is It Safe for Dogs?, U.S. Food & Drug Administration (FDA)
• BSE (Mad Cow) Detected; Food supply "Safe", FoodSafety.gov
• FDA MedWatch - Roche Diagnostics Operations Elecsys Troponin I and Elecsys Troponin I STAT Immunoassays: Recall – Doctors may receive a falsely low result, FDA MedWatch
• CVM Updates - FDA Announces Final Strategic Plan for the Foods and Veterinary Medicine Program, U.S. Food & Drug Administration (FDA)
• FDA strengthens international collaboration to ensure quality, safety of imported products, U.S. Food & Drug Administration (FDA)
• Report: FDA strengthens monitoring of post-approval drug safety, U.S. Food & Drug Administration (FDA)
• RECALL: Sausage Products: Misbranding and Undeclared Allergen, FoodSafety.gov
• RECALL: Calzone Products for Possible Listeria Contamination, FoodSafety.gov
• XROCK INDUSTRIES, LLC Issues a Voluntary Nationwide Recall of X-ROCK, a Product Marketed as a Dietary Supplement To Support Male Sexual Performance, Due to Unlisted, Potentially Hazardous Ingredient, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Victrelis (boceprevir) label change reflects drug-drug interaction information with HIV protease inhibitors, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Certain Compounded Drugs from Franck's: FDA Issues Second Warning to Physicians, FDA MedWatch
• Update of CVM's What's New - Letters to Veterinary Professionals, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Aliskiren-containing Medications: Drug Safety Comunication - New Warning and Contraindication, FDA MedWatch
• HIV/AIDS Update - Isentress label update includes 156-week safety and efficacy data, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Second Annual Report Posted for the Reportable Food Registry, U.S. Food & Drug Administration (FDA)
• RECALL: Undeclared Sulfites In Peacock Brand Preserved Apricots, FoodSafety.gov
• Hong Lee Trading Inc. Issues An Alert On Undeclared Sulfites In Peacock Brand Preserved Apricots, U.S. Food & Drug Administration (FDA)
• Health Coverage for Young Adults Under 26 - It's Abby-Care!, HealthCare.gov
• Enforcement Report for April 18, 2012, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Other‐Sonic Generic Ultrasound Transmission Gel: Safety Communication - Risk of Bacterial Contamination, FDA MedWatch
• RECALL: Baby Bird & Baby Macaw Feeding Formula, FoodSafety.gov
• RECALL: Stouffer's Lasagna Due to Mislabeling, FoodSafety.gov
• RECALL: Sub Sandwiches Because of Possible Listeria, FoodSafety.gov
• M.E. Thompson, Inc. Expands Recall of Sub Sandwiches Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Morphine Sulfate Injection USP, 4 mg/mL (C-II), 1 mL fill in 2.5 mL Carpuject by Hospira, Inc: Recall - May Contain More Than Intended Fill Volume, FDA MedWatch
• Hospira Announces a Nationwide Voluntary Recall of One Lot of Morphine Sulfate Injection, USP 4 MG/ML, (C-II) 1 ML Fill in 2.5 ML Carpuject, That May Contain More Than The Intended Fill Volume, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Product Recall Information of Baby Bird & Baby Macaw Feeding Formula, U.S. Food & Drug Administration (FDA)
• Notice of Recall, U.S. Food & Drug Administration (FDA)
• Product Recall Information of Baby Bird & Baby Macaw Feeding Formula, U.S. Food & Drug Administration (FDA)
• MyCare Stories: Robyn in Baltimore, MD, HealthCare.gov
• Update of CVM's What's New - Minutes of Meetings Available; Industry Discussions on AGDUFA II Reauthorization, U.S. Food & Drug Administration (FDA)
• RECALL: Dole Fresh Vegetables Salads, FoodSafety.gov
• RECALL: Frozen raw yellowfin tuna product associated with Salmonella, FoodSafety.gov
• ALERT: Undeclared Peanuts in Barbeque Almonds, FoodSafety.gov
• RECALL: Frozen raw yellowfin tuna product, FoodSafety.gov
• RECALL: Taco Dinner Kits Due to Possible Milk Allergen, FoodSafety.gov
• Food Lion Hard and Soft Taco Box, U.S. Food & Drug Administration (FDA)
• Harry and David Issues Allergy Alert on Undeclared Peanuts in Harry & David Premium Kansas City Style Barbeque Almonds, U.S. Food & Drug Administration (FDA)
• Mission Foods Voluntarily Recalls Taco Dinner Kits Due to Possible Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• Moon Marine USA Corporation voluntarily recalls frozen raw yellowfin tuna product “Nakaochi Scrape” associated with a multistate outbreak of Salmonella Bareilly infections, U.S. Food & Drug Administration (FDA)
• Kroger Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Kroger Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
• Kroger Taco Box, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Kroger Taco Box, U.S. Food & Drug Administration (FDA)
• Winn Dixie Taco Box, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Winn Dixie Taco Box, U.S. Food & Drug Administration (FDA)
• Hannaford Yellow Taco Box, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Hannaford Yellow Taco Box, U.S. Food & Drug Administration (FDA)
  • Hannaford Yellow Taco Box, U.S. Food & Drug Administration (FDA)
• Hannaford Yellow Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Hannaford Yellow Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • Hannaford Yellow Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
• Hannaford Soft and Hard Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Hannaford Soft and Hard Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • Hannaford Soft and Hard Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
• Winn Dixie Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Winn Dixie Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • Winn Dixie Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
• Dole Fresh Vegetables Announces Precautionary Recall of Limited Number of Salads, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 11, 2012, U.S. Food & Drug Administration (FDA)
• Food Lion Hard and Soft Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Food Lion Hard and Soft Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • Food Lion Hard and Soft Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
• CFP Online Application, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CFP Online Application, U.S. Food & Drug Administration (FDA)
• Hannafrd Soft and Hard Taco Box, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Hannafrd Soft and Hard Taco Box, U.S. Food & Drug Administration (FDA)
  • Hannafrd Soft and Hard Taco Box, U.S. Food & Drug Administration (FDA)
• Food Lion Yellow Taco Box, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Food Lion Yellow Taco Box, U.S. Food & Drug Administration (FDA)
  • Food Lion Yellow Taco Box, U.S. Food & Drug Administration (FDA)
• Food Lion Yellow Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Food Lion Yellow Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
  • Food Lion Yellow Taco Nutrition Label, U.S. Food & Drug Administration (FDA)
• RECALL: Undeclared Soy and Milk Ingredients in Snack Nut Blend Product, FoodSafety.gov
• RECALL: Undeclared Soy Ingredients In Vanilla Bean & Cocoa Mocha Almonds, FoodSafety.gov
• ALERT: Undeclared Allergens In Pies, Pasta, And Spreads, FoodSafety.gov
• H.C. Foods Co. Issues an Alert on Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• John B. Sanfilippo and Son, Inc. Voluntarily Recalls Full Circle Concierge Snack Nut Blend Product Due to Undeclared Soy and Milk Ingredients, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Report of FY 2010 Nationwide Survey of Distillers Products for Antibiotic Residues, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Monthly Safety Labeling Changes includes 39 products with revisions to Prescribing Information, FDA MedWatch
• Update of CVM's What's New - Updated Current Drug Shortage Information, U.S. Food & Drug Administration (FDA)
• John B. Sanfilippo and Son, Inc. Voluntarily Recalls Fisher Vanilla Bean Almonds and Fisher Cocoa Mocha Almonds Product Due to Undeclared Soy Ingredients, U.S. Food & Drug Administration (FDA)
• Mediterra S.A. Issues Allergy Alert On Undeclared Allergens In Mastihashop Brand Pies, Pasta, And Spreads, U.S. Food & Drug Administration (FDA)
• RECALL: Ground and Tenderized Beef Products Due to Possible E. Coli, FoodSafety.gov
• ALERT: Undeclared Peanut Allergen in Classic Caramel Cob Junior, FoodSafety.gov
• RECALL: Uneviscerated Fish May Contain Botulinum Spores, FoodSafety.gov
  • <Possible follow-ups>
  • RECALL: Uneviscerated Fish may contain Botulinum Spores, FoodSafety.gov
• Kathy Kaye Foods, LLC Issues Allergy Alert on Undeclared Peanut Allergen in Classic Caramel Cob Junior, U.S. Food & Drug Administration (FDA)
• Dept. of Justice enters consent decree with California seafood processor, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA takes steps to protect public health, U.S. Food & Drug Administration (FDA)
• Import Foods Wholesale, Inc Issues An Alert On Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• MyCare Stories: Nancy C. in North Conway, NH, HealthCare.gov
• RECALL: Uneviscerated Fish, FoodSafety.gov
• Seng Ong Wholesale, Inc. Issues An Alert On Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• RECALL: Dry Dog Food Bags May Contain Salmonella, FoodSafety.gov
• Update of CVM's What's New - Diamond Pet Foods Voluntarily Recalls Limited Number of Dry Dog Food Bags Due to a Potential Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Birth Control Pills Containing Drospirenone: Label Change-Products may be associated with a higher risk for blood clots, FDA MedWatch
• RECALL: "Any Wine Will Do" Cermanic Wine Goblet, FoodSafety.gov
• Diamond Pet Foods Voluntarily Recalls Limited Number of Dry Dog Food Bags Due to a Potential Health Risk Recall is limited to one formula of Diamond Naturals distributed to 12 states; no illnesses reported, U.S. Food & Drug Administration (FDA)
• Food Lion Manufacturer Recalls Store Brand Hard/Soft Taco Dinner Kit Recalled Products Were Produced Under the Food Lion Store Brand Label and Sold at Food Lion, Harveys and Reid’s Stores, U.S. Food & Drug Administration (FDA)
• Enesco Voluntarily Recalls “Any Wine Will Doâ€� Ceramic Wine Goblet, U.S. Food & Drug Administration (FDA)
• ALERT: Undeclared Milk in Knott's Berry Farm Cookies, FoodSafety.gov
• RECALL: Food Lion Hard/Soft Taco Dinner Kit, FoodSafety.gov
• ALERT: Undeclared Cashews In "Vegetable Biryani", FoodSafety.gov
• RECALL: Kraft Foods Planters Cocktail Peanuts, FoodSafety.gov
• Food Lion Manufacturer Recalls Store Brand Hard/Soft Taco Dinner Kit Recalled Products Were Produced Under the Food Lion Store Brand Label and Sold at Food Lion, Harveys and Reid's Stores, U.S. Food & Drug Administration (FDA)
• Rajbhog Foods Inc Issues Allergy Alert On Undeclared Cashews In "Vegetable Biryani", U.S. Food & Drug Administration (FDA)
• Biscomerica Issues Allergy Alert on Undeclared Milk in it's Knott's Berry Farm 12/8/2 Boysenberry Cookies #59680, Bluberry Cookies #59675, Raspberry Cookies #59670 Strawberry Cookies #59695., U.S. Food & Drug Administration (FDA)
• Food Lion Manufacturer Recalls Store Brand Hard/Soft Taco Dinner Kit Recalled Products Were Produced Under the Food Lion Store Brand Label and Sold at Food Lion, Harveys and Reid’s Stores, U.S. Food & Drug Administration (FDA)
• Kraft Foods Voluntarily Recalls Single Code Date of Planters Cocktail Peanuts, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces the Approval of Two New Indications for Aquaflor, U.S. Food & Drug Administration (FDA)
• Alert: Glazers Donuts With Trace Egg, FoodSafety.gov
• FDA announces plans to pilot end-stage kidney disease technology in new program, U.S. Food & Drug Administration (FDA)
• Allergen Alert: Glazers Donuts With Trace Egg, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - ADE Reports and Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• RECALL: Steamed BBQ Flavored Pork Buns Contain MSG, FoodSafety.gov
• ALERT: Undeclared Milk Allergens, FoodSafety.gov
• Odwalla, Inc. Issues Nationwide Allergy Alert On Chocolate Protein Monster Beverage, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Odwalla, Inc. Issues Nationwide Allergy Alert On Chocolate Protein Monster Beverage, FoodSafety.gov
• CVM Updates - Cephalosporin Order of Prohibition Goes Into Effect, U.S. Food & Drug Administration (FDA)
• Los Olivos LTD Issues Allergy Alert On Undeclared Milk Allergens In "Los Olivos LTD Pan de Torta", U.S. Food & Drug Administration (FDA)
• FDA Press Release, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA Press Release, FoodSafety.gov
• Threeline Imports, Inc Issues Allergy Alert On Undeclared Eggs In Kypoyka Bisquit In a 21.16 Oz Cardboard Box, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Threeline Imports, Inc Issues Allergy Alert On Undeclared Eggs In Kypoyka Bisquit In a 21.16 Oz Cardboard Box, FoodSafety.gov
• HIV/AIDS Update - Blood Products Advisory Committee Mtg, May 15-16, 2012, In-Home HIV Test, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 4, 2012, U.S. Food & Drug Administration (FDA)
• RECALL: Undeclared Milk on Coconut Candy, FoodSafety.gov
• Update of CVM's What's New - Role of the Food Safety Modernization Act in Ensuring the Safety of Pet Food, U.S. Food & Drug Administration (FDA)
• Fung Shing International Corp Issues an Alert on Undeclared Milk on Coconut Candy, Keo Dua La Dua, U.S. Food & Drug Administration (FDA)
• Fung Shing International Corp Issues An Alert On Undeclared Milk On Cocunut Candy, Keo Dua, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Thoratec Corporation, HeartMate II Left Ventricular Assist System (LVAS): Class 1 Recall- Outflow Graft May Kink or Deform, FDA MedWatch
• RECALL: Stuffed Potato Product Due To Undeclared Allergens, FoodSafety.gov
• American Regent Initiates Nationwide Voluntary Recall of Cyanocobalamin Injection, USP, 100 mcg/mL, 1ml Vial Lot #s 1662, 1679, 1683 Due to Cracks in the Vials, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Altuzan (bevacizumab): Counterfeit Product - Contains no Active Ingredient, FDA MedWatch
• The April 2012 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• MyCare: Peace of Mind and Health Coverage for People with Pre-Existing Conditions, HealthCare.gov
• National Public Health Week is April 2-8: Help a Healthier America Begin Today, U.S. Food & Drug Administration (FDA)
• RECALL: Chicken Sausage Products May Contain Foreign Materials, FoodSafety.gov
• RECALL: Vanilla Cream Puffs due to mislabeled Milk Allergen, FoodSafety.gov
• Update of CVM's What's New - Fish Food Recall, U.S. Food & Drug Administration (FDA)
• Creme Curls Bakery Recalls Vanilla Cream Puffs due to mislabeled Milk Allergen, U.S. Food & Drug Administration (FDA)
• The Hartz Mountain Corporation Recalls Four Lots of Wardley Advanced Nutrition Perfect Protein Tropical Flake Fish Food Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL: Jalapeno Peppers May Be Contaminated With Salmonella, FoodSafety.gov
• Obama administration takes action to address tobacco epidemic, U.S. Food & Drug Administration (FDA)
• South Florida Produce, LLC. Recalls Jalapeno Peppers Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL: Stuffed Beef Products Have Possible Listeria Contamination, FoodSafety.gov
• RECALL: Undeclared Milk In Chocolate Chip Chunk Cookies, FoodSafety.gov
• RECALL: Jalapeno Peppers Potentially Contaminated with Salmonella, FoodSafety.gov
• Topnotch Cookies & Cakes Issues Allergy Alert On Undeclared Milk In Chocolate Chip Chunk Cookies, U.S. Food & Drug Administration (FDA)
• Castellini Company LLC Recalls Jalapeno Peppers Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Isentress (raltegravir) label update, U.S. Food & Drug Administration (FDA)
• Latest Updates on MyCare: Dave's Story, HealthCare.gov
• RECALL: Salsa Products Potentially Contaminated with Salmonella, FoodSafety.gov
• FDA to discuss risks and benefits of metal-on-metal hip replacements, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 28, 2012, U.S. Food & Drug Administration (FDA)
• Club Chef LLC Recalls Salsa Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Updated HHS Adult and Adolescent Antiretroviral Treatment Guidelines available, U.S. Food & Drug Administration (FDA)
• RECALL: Undeclared Sulfites in Golden Smell Brand "Dried Potato", FoodSafety.gov
• FDA MedWatch - Celexa (citalopram hydrobromide) - Drug Safety Communication: Revised Recommendations, Potential Risk of Abnormal Heart Rhythms, FDA MedWatch
• RECALL: Pork and Beef Smoked Sausage, FoodSafety.gov
• Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designation List, U.S. Food & Drug Administration (FDA)
• FDA approves Omontys to treat anemia in adult patients on dialysis, U.S. Food & Drug Administration (FDA)
• New FDA guidance on considerations used in device approval, de novo decisions, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - May 11 FDA advisory committee meeting:fixed-dose combination tablet of elvitegravir/cobicistat/emtricitabine/ tenofovir disoproxil fumarate, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Intelence (etravirine): pediatric dosing recommendations and new scored 25 mg tablet for pediatric dosing, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - ADUFA III Negotiation Meeting Minutes – March 6, 2012, U.S. Food & Drug Administration (FDA)
• RECALL: Beef Patties Due To E. Coli, FoodSafety.gov
• RECALL: Imported Canadian Ground Beef Patties, FoodSafety.gov
• RECALL: Queso Fresco El Ranchero Del Sur and Other Cheeses, FoodSafety.gov
• El Ranchero Del Sur, LLC. Recalls Queso Fresco El Ranchero Del Sur (Fresh Cheese), Queso Fresco En Hoja De Platano Los Corrales (Fresh Cheese in Banana Leaf), and Queso Hebra Queso Oaxaca El Ranchero Del Sur (String Cheese) Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• El Ranchero Del Sur, LLC. Recall (Esta Piendo Devolución) Queso Fresco El Ranchero Del Sur, Queso Fresco En Hoja De Platano Los Corrales, Y Queso Hebra Queso Oaxaca El Ranchero Del Sur Debido A Posible Reigos De Salud, U.S. Food & Drug Administration (FDA)
• The Affordable Care Act and You: Two Years Later, HealthCare.gov
• ALLERGY ALERT: Mini Chocolate Chip Cookies Sold in Whole Foods Markets, FoodSafety.gov
• RECALL: Beef Sausage Due to Listeria, FoodSafety.gov
• RECALL: Pork - Recall Notification Report 015-2012, FoodSafety.gov
• RECALL: El Ranchero Queso Fresco (Fresh Cheese) and other Cheeses, FoodSafety.gov
• Second Anniversary of the Affordable Care Act: Statement by Secretary Sebelius, HealthCare.gov
• FDA MedWatch - Argatroban Injection 50 mg/50 mL (1 mg/mL): Recall - Potential for Visible Particulates, FDA MedWatch
• Eagle Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of 4 Lots of Argatroban Injection 50 mg/50 mL (1 mg/mL) Due to a Potential for Visible Particulates. NDC# 42367-203-07 (single unit) NDC# 42367-203-84 (10 pack), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Application Deadline for Student Internships has been extended to April 6, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 21, 2012, U.S. Food & Drug Administration (FDA)
• Latest Updates From HealthCare.gov - Mark's Story: MyCare for Small Businesses, HealthCare.gov
• Whole Foods Market issues allergy alert for undeclared walnuts in Mini Chocolate Chip Cookies, U.S. Food & Drug Administration (FDA)
• Thoratec Corporation Issues Update on Worldwide Medical Device Correction Notification Relating to Sealed Outflow Graft Used With HeartMate II Left Ventricular Assist System, U.S. Food & Drug Administration (FDA)
• FDA approves LINX Reflux Management System to treat gastroesophageal reflux disease, U.S. Food & Drug Administration (FDA)
• Steven's Story: MyCare for Young Adults - HealthCare.gov, HealthCare.gov
• Update of CVM's What's New - Safe Handling of Pet Food in the Home Video, U.S. Food & Drug Administration (FDA)
• Vanessa's Story: MyCare for Women - HealthCare.gov, HealthCare.gov
• FDA approves first Boniva generics to treat or prevent osteoporosis, U.S. Food & Drug Administration (FDA)
• El Ranchero Del Sur, LLC Recalls El Ranchero Queso Fresco (Fresh Cheese), Los Corrales Queso Fresco en Hoja de Platano (Fresh Cheese in Banana Leaf), and El Ranchero Queso Oaxaca (String Cheese) Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• MyCare for Seniors: Helen's Story, HealthCare.gov
• Introducing MyCare: Share Your Health Care Stories - HealthCare.gov, HealthCare.gov
• RECALL: Chicken Caesar Wraps Sold in California, FoodSafety.gov
• FDA MedWatch - Brilliant Blue G: Recall of Unapproved Drug - Ongoing Investigation of Fungal Endophthalmitis Cases, FDA MedWatch
• RECALL: Caramel Puffcorn Sold in 32 States, FoodSafety.gov
• Troyer Cheese, Inc. Recalls Backroad Country Caramel Puffcorn Sold in 8oz and 16oz Plastic Bags Because of Undeclared Milk, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Statement on Compounding of Pergolide Products for Animal Use, U.S. Food & Drug Administration (FDA)
• Recall of Brilliant Blue G Urgent Product Recall - Immediate Action Required, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - May 10 FDA advisory committee meeting: Truvada for Pre-Exposure Prophylaxis (PrEP), U.S. Food & Drug Administration (FDA)
• The MedWatch February 2012 Safety Labeling Changes posting includes 65 products with safety labeling changes, FDA MedWatch
• FDA MedWatch - Skin Creams, Soaps and Lotions Marketed as Skin Lighteners and Anti-aging Treatments: May Contain the Toxic Metal, Mercury, FDA MedWatch
• Enforcement Report for March 14, 2012, U.S. Food & Drug Administration (FDA)
• FDA approves first generic Lexapro to treat depression and anxiety disorder, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Acclarent Inspira AIR Balloon Dilation System: Class 1 Recall - Potential For Balloon To Not Deflate Or To Deflate To Slowly, FDA MedWatch
• RECALL: Beef Stew Mix Distributed in AL, FL, GA, TN &SC, FoodSafety.gov
• Update of CVM's What's New - FY 2011 ADUFA Performance Report, U.S. Food & Drug Administration (FDA)
• Publix Issues Allergy Alert On Publix Beef Stew Mix, U.S. Food & Drug Administration (FDA)
• RECALL: Nutrena NatureWise Goat Pellets, FoodSafety.gov
• RECALL: Gerber Good Start Infant Formula, FoodSafety.gov
• FDA MedWatch - Gerber Good Start Gentle Powdered Infant Formula: Recall - Off-Odor, FDA MedWatch
• Update of CVM's What's New - Questions and Answers Regarding Chicken Jerky Treats from China, U.S. Food & Drug Administration (FDA)
• Cargill Animal Nutrition Conducts Regional Recall of Nutrena NatureWise Goat Pellets, U.S. Food & Drug Administration (FDA)
• FDA approves new silicone gel-filled breast implant, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA approves new silicone gel-filled breast implant, U.S. Food & Drug Administration (FDA)
  • FDA approves new silicone gel-filled breast implant, FDA Office of Women's Health
• Update of CVM's What's New - Cargill Animal Nutrition Conducts Regional Recall of Nutrena NatureWise ® Goat Pellets, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Veterinary Master Files listing, U.S. Food & Drug Administration (FDA)
• Gerber Voluntarily Withdraws a Specific Batch of Gerber® Good Start® Infant Formula and Offers Replacement Product to Consumers, U.S. Food & Drug Administration (FDA)
• FDA Commissioner Margaret A. Hamburg's Statement on the Surgeon General's Report, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Guidance for Industry: Testing for Salmonella Species in Human Foods and Direct-Human-Contact Animal Foods, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 7 2012, U.S. Food & Drug Administration (FDA)
• Bedford Laboratories™ Issues Nationwide Voluntary Recall of Cytarabine for Injection, USP, 1 Gram per Vial, U.S. Food & Drug Administration (FDA)
• RECALL: Pizza Toppings, FoodSafety.gov
• Update of CVM's What's New - Guidance Available, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Guidance Available, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Guidance Available, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Guidance Available, U.S. Food & Drug Administration (FDA)
• FDA approves Surfaxin to prevent breathing disorder in premature infants, U.S. Food & Drug Administration (FDA)
• Appointment of Assistant Commissioner for Women's Health, U.S. Food & Drug Administration (FDA)
• RECALL: Streusel Topped Fruit Pies, FoodSafety.gov
• Price Chopper Supermarkets Recalls Streusel Topped Fruit Pies, U.S. Food & Drug Administration (FDA)
• RECALL: Ready-To-Eat Pizza Stick Products, FoodSafety.gov
• RECALL: Horse and Animal Feed Distributed In Nebraska & Wyoming, FoodSafety.gov
• Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Western Feed, LLC Conducts Voluntary Recall Of Feed Distributed In Nebraska And Wyoming, U.S. Food & Drug Administration (FDA)
• Western Feed, LLC Conducts Voluntary Recall Of Feed Distributed In Nebraska And Wyoming, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cardiac Science Powerheart, CardioVive, CardioLife; GE Responder and Responder Pro; and Nihon-Kohden Automated External Defibrillators (AEDs): Class I Recall - Defective Component, FDA MedWatch
• HIV/AIDS Update - Important info about interactions between certain HIV drugs and cholesterol-lowering statin drugs, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Important info about interactions between certain hepatitis C drugs and cholesterol-lowering statin drugs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Statins and HIV or Hepatitis C Drugs: Drug Safety Communication - Interaction Increases Risk of Muscle Injury, FDA MedWatch
• CVM Updates - - FDA Announces Availability of the 2010 NARMS Retail Meat Annual Report, U.S. Food & Drug Administration (FDA)
• FDA approves two new pancreatic enzyme products to aid food digestion, U.S. Food & Drug Administration (FDA)
• RECALL: Recall Notification Report on Breakfast Sausage, FoodSafety.gov
• Enforcement Report for February 29 2012, U.S. Food & Drug Administration (FDA)
• The March 2012 MedSun Newsletter is now available, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Flight Medical V24-00400-29 Cable for Newport HT50 Ventilator: Class I Recall – Cable May Cause an Electrical Shortage That can Cause Ventilators to Shutdown Unexpectedly, FDA MedWatch
• FDA announces safety changes in labeling for some cholesterol-lowering drugs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Statin Drugs - Drug Safety Communication: Class Labeling Change, FDA MedWatch
• FDA MedWatch - Norgestimate and Ethinyl Estradiol Tablets: Recall - Packaging Error, Potential for Incorrect Dosing Regimen, FDA MedWatch
• Regeneca, Inc. Issues a Voluntary Nationwide Recall of All Lots of Single Capsule RegenErect Because of Potential Health Risks, U.S. Food & Drug Administration (FDA)
• Glenmark Generics Inc. Announces a Nationwide Recall of Seven (7) Lots of Norgestimate and Ethinyl Estradiol Tablets USP, 0.18 mg/0.035 mg, 0.215 mg/0.035 mg, 0.25 mg/0.035 mg (Generic) Due to Possibility of Out of Sequence Tablets, U.S. Food & Drug Administration (FDA)
• FDA approves first Helicobacter pylori breath test for children, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nemschoff Chairs Perinatal Pediatric Hospital Bed (Bassinet): Class 1 Recall - Risk of Injury to Patients, FDA MedWatch
• Update of CVM's What's New - FY 2011 AGDUFA Performance Report, U.S. Food & Drug Administration (FDA)
• Cytarabine for Injection, 1 gm/vial [Bedford Labs]: Recall: Risk of Lack of Sterility, U.S. Food & Drug Administration (FDA)
• American Regent Injectable Products: Recall - Visible Particulates in Products, U.S. Food & Drug Administration (FDA)
• Bedford Laboratoriesâ„¢ Issues Nationwide Voluntary Recall of Cytarabine for Injection, USP, 1 Gram per Vial, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Smiths Medical Bivona Neonatal, Pediatric and Flextend Tracheostomy Tubes: Class 1 Recall - Inadvertent Dislodgement, U.S. Food & Drug Administration (FDA)
• RECALL: Non-alcoholic Malta Beverages, FoodSafety.gov
• Enforcement Report for February 22, 2012, U.S. Food & Drug Administration (FDA)
• Voluntary Recall Of Goya, Great Value, Hatuey, Mr. Special, Polar, Publix, Regal, And SuperMax Brand Malta Beverages In 7-oz Bottles Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall Of Phenylephrine HCl Injection, USP, 1% 5 mL Vial, Lot# 0693 Due To Visible Particles, U.S. Food & Drug Administration (FDA)
• FDA MedWatch, U.S. Food & Drug Administration (FDA)
• FDA Office of Women's Health Winter eUpdate, U.S. Food & Drug Administration (FDA)
• Healthy People Co. is Expanding its Voluntary Recall Initiated on February 02, 2012 to Include Dietary Products Bought on or Before October 25, 2011, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Clarifies use of the Term, “Non-lactating Dairy Cattle”, U.S. Food & Drug Administration (FDA)
• FDA acts to bolster supply of critically needed cancer drugs, U.S. Food & Drug Administration (FDA)
• FDA approves Korlym for patients with endogenous Cushing’s syndrome, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Infants’ TYLENOL Oral Suspension, 1 oz. Grape: Recall - Dosing System Complaints, FDA MedWatch
• McNeil Consumer Healthcare Announces Voluntary Nationwide Recall of Infants’ TYLENOL® Oral Suspension, 1 oz. Grape Due to Dosing System Complaints, U.S. Food & Drug Administration (FDA)
• RECALL: Chili Products, FoodSafety.gov
• RECALL: Meat and Poultry, FoodSafety.gov
• Update of CVM's What's New - Now accepting student internship applications, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Spinbrush Powered Toothbrush by Arm and Hammer or Crest: Safety Communication - Choking Hazard and Serious Injuries, FDA MedWatch
• Enforcement Report for February 15, 2012, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Avastin (bevacizumab): Counterfeit Product - FDA Issues Letters to 19 Medical Practices, FDA MedWatch
• Flight Medical Innovations Ltd. Provides Update on Recall of Ventilator Remote Alarm Cable, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Basics Webinar on Advice to Dog Owners Whose Pets Take NSAIDS, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Salter Labs 7600 Bubble Humidifier Used with Supplemental Oxygen Therapy: Class I Recall - Humidifier Lids Fail to Pop Off at the Intended Pressure, FDA MedWatch
• Update of CVM's What's New - FDA seeks $4.5 billion to support medical product development, protect patients and ensure safety of the food supply, U.S. Food & Drug Administration (FDA)
• FDA seeks $4.5 billion to support medical product development, protect patients and ensure safety of the food supply, U.S. Food & Drug Administration (FDA)
• New Jersey company agrees to halt production of unapproved dental devices, U.S. Food & Drug Administration (FDA)
• RECALL: Cruller Bakery Pastries Distributed in Walmart Due To Mislabeled Milk Allergen, FoodSafety.gov
• RECALL: Pumpkin Bundt Cakes Distributed in Whole Foods Market Stores in CA, FoodSafety.gov
• FDA MedWatch - RegenArouse: Recall - Undeclared Drug Ingredient, FDA MedWatch
• FDA MedWatch - January 2012 Safety Labeling Changes posting includes 63 products, FDA MedWatch
• Whole Foods Market Recalls Pumpkin Bundt Cakes For Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Walmart Recalls Cruller Bakery Pastries Due To Mislabeled Milk Allergen, U.S. Food & Drug Administration (FDA)
• Regeneca, Inc. Issues A Voluntary Nationwide Recall Of A Specific Lot Of RegenArouse Because Of Potential Health Risks, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Wholistic Herbs, Inc. "Koff and Kold" and "Kold Sore" Spray: Recall - Non-Sterile Products, FDA MedWatch
• FDA MedWatch - Hand-held Dental X-Ray Units: FDA Safety Communication - Unreviewed Products May Not Be Safe or Effective, FDA MedWatch
• RECALL: Cooked Pork Hocks, FoodSafety.gov
• ALLERGY ALERT: Eggs in Bin Bin Snow Rice Cracker, FoodSafety.gov
• RECALL: Update on Sliced Herring Fillet Recall Due to Listeria, FoodSafety.gov
• Update of CVM's What's New - Webinar Materials Available - What You Need to Know: FDA-Approved vs. Unapproved Animal Drugs, U.S. Food & Drug Administration (FDA)
• Summit Import Corporation Issues Allergy Alert on Undeclared Eggs in Bin Bin Snow Rice Cracker 5.3oz Pack and Bin Bin Rice Cracker 15.8oz Bulk Pack, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA investigating illegal online sale of handheld dental X-ray units, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Public Meeting to Discuss Antiparasitic Drug Use and Resistance in Ruminants and Equines, U.S. Food & Drug Administration (FDA)
• Allison's Gourmet Kitchens Recalls Prepared Salads that Contain Hard Cooked Eggs Due to Potential Health Risk., U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Victrelis (boceprevir) and Ritonavir-Boosted HIV Protease Inhibitor Drugs - Drug Interactions, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Victrelis (boceprevir) and Ritonavir-Boosted Human Immunodeficiency Virus (HIV) Protease Inhibitor Drugs - Drug Interactions, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Victrelis (boceprevir) and Ritonavir-Boosted Human Immunodeficiency Virus (HIV) Protease Inhibitor Drugs: Drug Safety Communication - Drug Interactions, FDA MedWatch
  • <Possible follow-ups>
  • FDA MedWatch - Victrelis (boceprevir) and Ritonavir-Boosted Human Immunodeficiency Virus (HIV) Protease Inhibitor Drugs: Drug Safety Communication - Drug Interactions, FDA MedWatch
• FDA issues draft guidance on biosimilar product development, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 8, 2012, U.S. Food & Drug Administration (FDA)
• RECALL: Egg Spread, Sandwiches, and Salads, FoodSafety.gov
• RECALL: Egg Salad Sandwiches, FoodSafety.gov
• Spartan Stores Voluntary Product Withdraw Notice, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tenative approval of lamivudine, nevirapine, and zidovudine fixed dose combination / PEPFAR, U.S. Food & Drug Administration (FDA)
• 50 Years after Thalidomide: Why Regulation Matters, U.S. Food & Drug Administration (FDA)
• Grand Strand Sandwich Company Recalls “Chicken Salad Sandwichesâ€� That May Contain Contaminated Hard Cooked Eggs Produced by Michael Foods., U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Proton Pump Inhibitors (PPIs) - Drug Safety Communication: Clostridum Difficile-Associated Diarrhea (CDAD) Can be Associated With Stomach Acid Drugs, FDA MedWatch
• RECALL: Chicken Salad Due To Listeria, FoodSafety.gov
• Statement from Secretary Sebelius on American Heart Month, U.S. Food & Drug Administration (FDA)
• North American Rescue, LLC Announces A Follow-Up to the Recall of Crickit Convenience Kits Because of Possible Health Risk Related to Nationwide Recall of Triad Povidone Iodine Prep Pads, U.S. Food & Drug Administration (FDA)
• RECALL: Strawberry Jam & Peanut Butter Snack Size Sandwich Bars, FoodSafety.gov
• RECALL: Cobb and Spinach Salads Due to Listeria, FoodSafety.gov
• RECALL: Prepared Sandwiches that Contain Cooked Eggs, FoodSafety.gov
• Update of CVM's What's New - February 2012 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• Healthy People Co. Issues a Voluntary Recall of Specific Lots of the Dietary Supplements Found to Contain Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• Nest Collective Voluntarily Recalls Select Revolution Foods Jammy Sammy - Strawberry Jam & Peanut Butter Snack Size Sandwich Bars Due to a Labeling Error (Undeclared Peanut on Inner Wrapper), U.S. Food & Drug Administration (FDA)
• California Firm Recalls Prepared Sandwiches that Contain Hard-Cooked Eggs, U.S. Food & Drug Administration (FDA)
• Greencore, USA – Cincinnati, Recalls Egg Salad Sandwiches with Brand Name Quick Café and Take Away Café because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL: Cobb Salads Due To Listeria, FoodSafety.gov
• RECALL: Salads Due to Listeria, FoodSafety.gov
• RECALL: Prepared Salads that Contain Hard Cooked Eggs, FoodSafety.gov
• RECALL: Various Prepared Foods That Contain Hard-Cooked Eggs, FoodSafety.gov
• RECALL: Zhang Zhou Brand Tremella Due to Undeclared Sulfites, FoodSafety.gov
• Pedinol Pharmacal Inc. Announces Health Advisory for Gris-PEG (griseofulvin ultramicrosize) 125mg and 250mg, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 1, 2012, U.S. Food & Drug Administration (FDA)
• Wegmans Recalls Various Prepared Foods That Contain Hard-Cooked Eggs Produced by Michael Foods, U.S. Food & Drug Administration (FDA)
• Allison’s Gourmet Kitchens Recalls Prepared Salads that Contain Hard Cooked Eggs Due to Potential Health Risk., U.S. Food & Drug Administration (FDA)
• Bedford Laboratories Issues A Voluntary Nationwide Patient Level Recall Of Acetylcysteine Solution, USP, LOT 1877093, U.S. Food & Drug Administration (FDA)
• RECALL: UPDATE: Corrected Lot Numbers: Advanced Animal Nutrition Dog Power Dry Dog Food Distributed in MO, AK, LA, FoodSafety.gov
• RECALL: Un-eviscerated "Rely" Sardine Anchovies for possible Botulium, FoodSafety.gov
• RECALL: On Un-Eviscerated "Rely" Dried Yellow Croaker for Possible Botulium, FoodSafety.gov
• Update of CVM's What's New - Corrected Lot Numbers for Advanced Animal Nutrition Dog Power Dog Food Recall, U.S. Food & Drug Administration (FDA)
• CVM Updates - February 2012 Update on Feed Enforcement Activities to Limit the Spread of BSE, U.S. Food & Drug Administration (FDA)
• S&M USA Enterprise Issues an Alert on Undeclared Sulfites in Zhang Zhou Brand Tremella, U.S. Food & Drug Administration (FDA)
• Updated News Release With Corrected Lot Numbers: Advanced Animal Nutrition Recalls Dog Power Dry Dog Food, U.S. Food & Drug Administration (FDA)
• W & C International Import Inc. Issues An Alert On Un-Eviscerated "Rely" Dried Yellow Croaker, U.S. Food & Drug Administration (FDA)
• W & C International Import Inc. Issues an Alert on Un-eviscerated “Relyâ€� Sardine Anchovies, U.S. Food & Drug Administration (FDA)
• RECALL: Hard-Cooked Eggs Packed In Brine Sold In 10- And 25-Pound Pails Because Of Possible Listeria, FoodSafety.gov
• Michael Foods Recalls Hard-Cooked Eggs Packed In Brine Sold In 10- And 25-Pound Pails Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Birth Control Pills Recalled, U.S. Food & Drug Administration (FDA)
• FDA and industry reach agreement in principle on medical device user fees, U.S. Food & Drug Administration (FDA)
• RECALL: Bin-Bin Snow Rice Crackers and Bin-Bin Rice Crackers Recall For Undeclared Egg, FoodSafety.gov
• ALLERGY ALERT: How Sweet is Fudge "Peanut Butter Buckeye" and "Peanut Butter Smoothie" from 01/23/2012 and earlier for Undeclared Milk, FoodSafety.gov
• FDA MedWatch - Lo/Ovral-28 (Norgestrel/EthinylEstradiol) Tablets: Recall - Possibility of Inexact Tablet Counts or Out of Sequence Tablets, FDA MedWatch
• How Sweet It Is Fudge and Candy Company, East Lansing, Michigan, Allergy Alert On Undeclared Milk Allergens In Products "Peanut Butter Buckeye" and “Peanut Butter Smoothieâ€� Date Code 01/23/2012 and Earlier, U.S. Food & Drug Administration (FDA)
• Pfizer Announces Voluntary Nationwide Recall of Lo/Ovral-28 and Norgestrel/Ethinyl Estradiol Tablets Due to Possibility of Inexact Tablet Counts or Out of Sequence Tablets, U.S. Food & Drug Administration (FDA)
• President Global Corporation Announces Bin-Bin Snow Rice Crackers and Bin-Bin Rice Crackers Recall For Undeclared Egg, U.S. Food & Drug Administration (FDA)
• Gemini Food Corporation and Tong Enterprises Announces Bin-Bin Snow Rice Crackers and Bin-Bin Rice Crackers Recall For Undeclared Egg, U.S. Food & Drug Administration (FDA)
• FDA approves Gleevec for expanded use in patients with rare gastrointestinal cancer, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of abacavir sulfate and lamivudine tablets 60mg/30mg for pediatric patients, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tenetative approval for abacavir sulfate / lamivudine tablets, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Presentations from the 2011 ADUFA/AGDUFA Public Meetings, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vitaflo USA Renastart: Recall - Possible Health Risk Due To Incorrectly Labeled Cans, FDA MedWatch
• The February 2012 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Vitaflo USA Announces Nationwide Voluntary Recall of Renastart 14.11 oz (400g) Cans Batch Number 12832 Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Vitaflo USA Announces Nationwide Voluntary Recall of Renastart 14.11 oz (400g) Cans Batch Number 12832 Due to Possible Health Risk, FoodSafety.gov
• FDA approves Kalydeco to treat rare form of cystic fibrosis, U.S. Food & Drug Administration (FDA)
• AVEENO BABY CALMING COMFORT LOTION, U.S. Food & Drug Administration (FDA)
• RECALL: Certain Lots of Walgreen's 13 Oz. Chocolate-Covered RaisinsMay Contain Peanuts, Almonds, Soy Due to Packaging Error, FoodSafety.gov
• Walgreen Co. Voluntarily Recalls Certain Lots of 13 Oz. Chocolate-Covered Raisins As Product May Contain Peanuts, Almonds, Soy Due to Packaging Error, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Treanda (bendamustine HCL): Recall - Particulate Matter in Vial, FDA MedWatch
• Cephalon, Inc. issues a voluntary nationwide recall of Treanda® (bendamustine HCL) for Injection 25mg/Vial Due to Particulate Matter, U.S. Food & Drug Administration (FDA)
• Pinnacle Foods Group LLC Issues Allergy Alert On Undeclared Soy Protein In Aunt Jemima Frozen Pancakes, U.S. Food & Drug Administration (FDA)
• RECALL: Turkey & Ham Footlong Sandwich, FoodSafety.gov
• FDA approves Inlyta to treat patients with a type of advanced kidney cancer, U.S. Food & Drug Administration (FDA)
• JKS Wholesale SVCS, Allergy Alert On Undeclared Milk Allergens In Torta de Pan Date Code 02/15/2012, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 25, 2012, U.S. Food & Drug Administration (FDA)
• M.E. Thompson, Inc. Recalls Anytime Deli Brand Turkey & Ham Footlong Sandwich Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Department of Justice files Consent Decree of Permanent injunction against Ranbaxy, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Green Book On-Line, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Green Book On-line, U.S. Food & Drug Administration (FDA)
• RECALL: Salt Distributed in CA, MN, WA Due to Salmonella, FoodSafety.gov
• RECALL: Shredded Taco Cheese Distributed in NY, VT, CT, PA, MA & NH, FoodSafety.gov