FDA News Releases

• Date Index

• Enforcement Report for July 16, 2014, U.S. Food & Drug Administration (FDA)
• Mars Food North America Voluntarily Recalls Specific Batch and Item Number Representing Less Than 2,000 Cases, U.S. Food & Drug Administration (FDA)
• FDA approves new product to treat rare genetic disease, U.S. Food & Drug Administration (FDA)
• Updated: Voluntary Nationwide Recall of Tattoo Ink, Tattoo Needles, Tattoo kits due to Microbial contamination, U.S. Food & Drug Administration (FDA)
• Baxter Initiates Voluntary Worldwide Recall Of Four Lots Of IV Solutions Due To The Presence Of Particulate Matter, U.S. Food & Drug Administration (FDA)
• Consejos de seguridad para el verano, GobiernoUSA.gov
• King of Pops Charleston SC Issues Allergen Alert on Undeclared: Soy, Milk, Egg and Wheat, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - June 2014 Safety Labeling Changes includes 52 products with revisions to Prescribing Information, FDA MedWatch
• Voluntary Nationwide Recall of Tattoo Ink, Tattoo Needles, Tattoo kits Due to Microbial Contamination, U.S. Food & Drug Administration (FDA)
• Sterile Drug Products by Unique Pharmaceuticals Ltd.: Recall - Lack of Sterility Assurance, FDA MedWatch
• Hospira Lactated Ringer's And 5% Dextrose Injection, 1000 ML, Flexible Containers: Recall (One Lot) - Mold Contamination, FDA MedWatch
• Hospira Issues Voluntary Nationwide Recall Of One Lot Of Lactated Ringers And 5% Dextrose Injection, Usp, 1000 Ml, Flexible Containers Due To Mold Contamination, U.S. Food & Drug Administration (FDA)
• Charles Products Recalls Decorative Pint And Shot Glasses Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 09, 2014, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Ventlab, LLC., Ventlab Manual Resuscitator, Duckbill Valve May Stick and Prevent Air from Getting to the Patient, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA to Hold Public Meeting on Antimicrobial Resistance Monitoring in the Food Supply, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Pre-packaged Mini Caesar And Mini Mesclun Goat Cheese Salad In Three States, Due To Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• Vascular Solutions, Inc. Issues Recall of Langston Dual Lumen Catheters, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Langston V2 Dual Lumen Catheters (Models 5540 and 5550) by Vascular Solutions: Class I Recall - Inner Catheter May Separate During Use and Cause Injury, FDA MedWatch
• FDA Classifies ConvaTec’s Voluntary Global Recall of Flexi-Seal™ CONTROL Fecal Management System (FMS) as Class I, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Vascular Solutions Langston V2 Dual Lumen Catheters (Models 5540 and 5550) - Inner Catheter May Separate During Use and Cause Injury, U.S. Food & Drug Administration (FDA)
• Huracán Arthur: esté preparado, GobiernoUSA.gov
• The July 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA approves Beleodaq to treat rare, aggressive form of non-Hodgkin lymphoma, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 02, 2014, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Medtronic Neurosurgery, Medtronic Duet External Drainage and Monitoring System - Patient Line Tubing May Disconnect and Lead to Injury, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medtronic Duet External Drainage and Monitoring System, Medtronic Neurosurgery: Class 1 Recall - Tubing May Disconnect and Lead to Injury, FDA MedWatch
• Update of CVM's What's New - Cargill Conducts Voluntary Recall of Select Nutrena® NatureWise® Meatbird Feed, U.S. Food & Drug Administration (FDA)
• Cargill Conducts Voluntary Recall of Select Nutrena® NatureWise® Meatbird Feed Due to Possible Animal Health Risk, U.S. Food & Drug Administration (FDA)
• Federal judge approves consent decree with New York dietary supplement maker, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals July 2014 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Oriya Organics, LLC Voluntarily Recalls Oriya Organics Superfood Protein Medley Containing Sprouted Chia Seed Powder for Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Mantenga su casa libre de plagas sin usar pesticidas, GobiernoUSA.gov
• FDA MedWatch - Coumadin (warfarin sodium) for Injection by Bristol-Myers Squibb: Recall - Particulate Matter, FDA MedWatch
• FDA seeks permanent injunction against California pharmaceutical company, U.S. Food & Drug Administration (FDA)
• Flowers Foods Issues Allergy Alert and Voluntary Recall on Limited Quantity of Sunbeam, Bunny, Flowers Deli, and Ingles Bar-B-Q Bread Sold in Alabama, Georgia, Louisiana, and Tennessee, U.S. Food & Drug Administration (FDA)
• Bristol-Myers Squibb Issues Voluntary Nationwide Recall of COUMADIN (Warfarin Sodium) for Injection Due to Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA outlines expectations for human drug compounders, including registered outsourcing facilities, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medical Supply Liquidators Injectable Vitamin Products With a "Sunshine Labs" Label: Warning - Products Not FDA Approved, FDA MedWatch
• CVM Updates - FDA Secures Full Industry Engagement on Antimicrobial Resistance Strategy, U.S. Food & Drug Administration (FDA)
• Medicines in My Home Update: OTC medicines and driving, U.S. Food & Drug Administration (FDA)
• FDA approves Afrezza to treat diabetes, U.S. Food & Drug Administration (FDA)
• Health Matters America Inc. Of Cheektowaga, New York, Recalls Additional Sprouted Chia Seed And Sprouted Chia & Flax Seed Powder Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 25, 2014, U.S. Food & Drug Administration (FDA)
• Kentucky oncology practice and its manager plead guilty to purchasing and selling unapproved chemotherapy drugs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lidocaine Viscous: Drug Safety Communication - Boxed Warning Required - Should Not Be Used to Treat Teething Pain, FDA MedWatch
• CVM Updates - FDA Issues Draft Guidance on the Use of Nanotechnology in Food for Animals, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: HydroFinity Hydrophilic Guidewire, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Over-The-Counter Topical Acne Products: Drug Safety Communication - Rare But Serious Hypersensitivity Reactions, FDA MedWatch
• Doctor’s Best Issues Voluntary Nationwide Recall of Red Yeast Rice due to Undeclared Lovastatin, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Olmesartan: Drug Safety Communication - FDA Review Finds Cardiovascular Risks for Diabetics Not Conclusive, FDA MedWatch
• FDA issues guidance to support the responsible development of nanotechnology products, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Provides Important Information to Veterinarians about PACCAL VET-CA1 for Treating Cancer in Dogs, U.S. Food & Drug Administration (FDA)
• New Article on Women in Medical Device Clinical Trials, FDA Office of Women's Health
• Update of CVM's What's New - Updated Current Animal Food GRAS Notices Inventory - AGRN 000-015, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated - Safe Use of Flea and Tick Products in Pets, U.S. Food & Drug Administration (FDA)
• Kraft Foods Group Voluntarily Recalls Small Quantity of Velveeta Original, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Big Sky Diagnostic Imaging, LLC in Butte, Montana: FDA Safety Communication - Mammography Problems, FDA MedWatch
• Medical Device Safety and Recalls:, U.S. Food & Drug Administration (FDA)
• FDA approves Sivextro to treat skin infections, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - ConvaTec, Inc., Flexi-Seal CONTROL Fecal Management System Kit: Class I Recall - Not Cleared for Marketing, FDA MedWatch
• Medical Device Safety and Recalls: ConvaTec, Inc., Flexi-Seal CONTROL Fecal Management System Kit - Not Cleared for Marketing, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Docetaxel: Drug Safety Communication - May Cause Symptoms of Alcohol Intoxication, FDA MedWatch
• FDA MedWatch - HydroFinity Hydrophilic Guidewires by NDC/Covidien: Recall - Outer Jacket Damage, FDA MedWatch
• Enforcement Report for June 18, 2014, U.S. Food & Drug Administration (FDA)
• NDC Implements Voluntary Recall of the Hydrofinity™ Hydrophilic Guidewire, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Marcaine (Bupivacaine HCI Injection, USP), 0.5 percent, 30 ML, Single-Dose, Preservative-Free Vial: Recall - Visible Particulates, FDA MedWatch
• Hospira Announces Voluntary Nationwide Recall of One Lot of 0.5% Marcaine™ (Bupivacaine HCI Injection, USP), 30 ML, Single-Dose, Preservative-Free Vial Due to Visible Particulates, U.S. Food & Drug Administration (FDA)
• Vita Food Products Issues Voluntary Recall of 4oz Vita Classic Premium Sliced Smoked Atlantic Salmon Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Domega NY International Co Ltd Issues Allergy Alert On Undeclared Peanuts And Milk In Gong Xifacai Gift Chocolates, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA to Reopen Comment Period on Reportable Food Registry ANPR, U.S. Food & Drug Administration (FDA)
• Wegmans Food Markets, Inc. Issues Allergy Alert on Undeclared Egg in Wegmans Cinnamon Raisin Buns, 12 oz., U.S. Food & Drug Administration (FDA)
• Schnucks Bakery Recalls Devil’s Food Cakes Topped With Undeclared Pecans, U.S. Food & Drug Administration (FDA)
• Smith's Country Cheese, Inc. Voluntarily RECALLS Waxed Gouda Wheels BECAUSE OF POSSIBLE HEALTH RISK, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - May 2014 Safety Labeling Changes includes 37 products with revisions to Prescribing Information, FDA MedWatch
• La Finquita Emite Una Alerta De Alergias Debido A Una Contaminacion Potencial De Mani O Cacahuate Y Frutos Secos En El Quesito Fresco Campesino, U.S. Food & Drug Administration (FDA)
• ¿Vale la pena cambiar de celular con un nuevo contrato?, GobiernoUSA.gov
• FDA MedWatch - Captomer and Captomer-250 by Thorne Research: FDA Warning - Potential Health Risks, FDA MedWatch
• FDA MedWatch - Smiths Medical Portex Low Dead Space Connector with Sideport, 3.5mm: Class I Recall- One Lot Mislabeled, FDA MedWatch
• FDA approves Lymphoseek to help determine the extent of head and neck cancer in the body, U.S. Food & Drug Administration (FDA)
• Fish Family Farm, Inc. Issues Allergy Alert On Milk Products And Cream Due To Potential Peanut And Tree Nut Contamination, U.S. Food & Drug Administration (FDA)
• La Finquita Cheese Issues An Allergy Alert Due To Potential Peanut And Tree Nut Contamination In Fresh Farmers Cheese, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Smiths Medical - Portex Low Dead Space Connector with Sideport, 3.5mm, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 11, 2014, U.S. Food & Drug Administration (FDA)
• Voluntary Product Recall: Wegmans Bagged Ice Due to Possible Metal Fragments - Sold in VA, MD, NJ, and some PA stores only, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Advocate Redi-Code+ Blood Glucose Test Strips by Diabetic Supply of Suncoast: Recall- Labeling Error, FDA MedWatch
• Princess House, Inc. hace un retiro voluntario de los Platos pequeños Marissa color mandarina debido a niveles de cadmio y plomo, U.S. Food & Drug Administration (FDA)
• Allergy Alert on Undeclared Milk in Dark Old Fashioned Sponge Candy, U.S. Food & Drug Administration (FDA)
• FDA Office of Women's Health June e-Update, FDA Office of Women's Health
• Diabetic Supply of Suncoast, Inc. issues a Nationwide Voluntary Recall of BMB-BA006A Advocate Redi-Code+ Blood Glucose Test Strips, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Meeting Minutes Available for the ADUFA III Conditional Approval Working Group, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listings - Medicated Feed Mill Licenses and VFD Distributor Notifications, U.S. Food & Drug Administration (FDA)
• Lansal, Inc. Voluntarily Recalls Egg White Salad With Chives Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• The June 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Dole Packaged Foods Recalls Roasted Garlic Tomato Basil Soup in Texas Due to Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• Olde Thompson Inc. Issues a Voluntary Recall of Kirkland Signature Coarse Ground Malabar Pepper 12.7 oz Plastic Jars Due to Possible Salmonella Risk, U.S. Food & Drug Administration (FDA)
• Navitas Naturals Expands Voluntary Recall for Organic Sprouted Chia Powder Products, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Changes to the Complera (emtricitabine/rilpivirine/tenofovir dispoproxil fumarate) labeling, U.S. Food & Drug Administration (FDA)
• FDA approves the first antihemophilic factor, Fc fusion protein for patients with Hemophilia A, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - New pediatric dosage form and label changes for Reyataz (atazanavir), U.S. Food & Drug Administration (FDA)
• GreenSmoothieGirl Issues Voluntary Recall for Organic Sprouted Chia Seed Powder Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Rite Aid Voluntarily Recalls 16 oz. Pints of Mint ‘N Chip Thrifty Ice Cream, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - PGG/HSC Feed Company LLC Issues Voluntary Recall of Champion Lamb Texturized Feed B30, U.S. Food & Drug Administration (FDA)
• PGG/HSC Feed Company LLC Issues Voluntary Recall of Champion Lamb Texturized Feed B30, Lot-88022114M908840, U.S. Food & Drug Administration (FDA)
• Ocean Spray Voluntarily Recalls Limited Quantity of 8-ounce Greek Yogurt Covered Craisins® Dried Cranberries Which May Contain Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• Health Matters America, Inc, Recalls Organic Sprouted Chia Seed Powder and Sprouted Chia/flax Seed Powder Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 04, 2014, U.S. Food & Drug Administration (FDA)
• Baptista’s Bakery Inc. Issues Voluntary Recall for LiveGfree Rosemary and Olive Oil Multiseed Snack Crackers, U.S. Food & Drug Administration (FDA)
• Glutino Voluntarily Recalls Glutino Rosemary and Olive Oil Snack Crackers (4.25 oz. and 20 oz.) Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals June 2014 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Cómo prepararse para la temporada de huracanes, GobiernoUSA.gov
• Update of CVM's What's New - Hill’s Pet Nutrition, Inc. Voluntarily Recalls 62 Bags of “Science Diet® Adult Small & Toy Breed™” Dry Dog Food, U.S. Food & Drug Administration (FDA)
• Hill’s Pet Nutrition, Inc. Voluntarily Recalls 62 Bags of “Science Diet® Adult Small & Toy Breed™” Dry Dog Food in California, Hawaii and Nevada Because of Potential Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Approves First Oral Drug for Fleas and Ticks in Dogs with Three Month Duration, U.S. Food & Drug Administration (FDA)
• Princess House, Inc. Voluntarily Recalls Marissa Tangerine Appetizer Plates Due to Cadmium and Lead Levels, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Soliris (eculizumab) Concentrated Solution for IV Infusion by Alexion: Recall - Visible Particulates, FDA MedWatch
• Alexion Initiates Voluntary Nationwide Recall of Certain Lots of Soliris® (eculizumab) Concentrated Solution for Intravenous Infusion Due to the Presence of Visible Particulate Matter in a Single Lot, U.S. Food & Drug Administration (FDA)
• FDA launches openFDA to provide easy access to valuable FDA public data, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Final Compliance Policy Guide on Food Facility Registration, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - June 17 Workshop on HIV Cure Research, U.S. Food & Drug Administration (FDA)
• FDA approves first generic versions of celecoxib, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 28, 2014, U.S. Food & Drug Administration (FDA)
• FDA allows marketing of first non-invasive test to help in identifying cause of certain kidney disease, U.S. Food & Drug Administration (FDA)
• FDA to require warnings on sunlamp products, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Pet Center, Inc. Voluntary Recall of 3 oz bag of Lamb Crunchy’s Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Navitas Naturals Issues Voluntary Recall for Organic Sprouted Chia Seed Powder Products, U.S. Food & Drug Administration (FDA)
• Eugene Oregon, Inc. Issues Voluntary Nationwide Expansion Of The Recall Of All Lots Of African Black Ant, Black Ant, And Mojo Risen Dietary Supplements Which May Contain Undeclared Active Pharmaceutical Ingredients, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Fresenius NaturaLyte Liquid Bicarbonate Concentrate (Part Number: 08-4000-LB), U.S. Food & Drug Administration (FDA)
• Pet Center, Inc. Voluntary Recall of 3 oz bag of Lamb Crunchy’s Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Rome Packing Co., Inc. Recalls Minced Crab Meat Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• American Importing Co, Inc Issues Allergy Alert On Undeclared Almonds Mispacked As Cinnamon Crunch Granola, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Import Tolerance for teflubenzuron available, U.S. Food & Drug Administration (FDA)
• Belleville Farmer’s Market Recalls Shelled Walnuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Sun Tree LLC Recalls 12oz Packaged California Grown Shelled Walnuts Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Brunkow Cheese Issues Allergy Alert On Undeclared Soy In Jalapeno Pepper Raw Milk Cheddar Cold Pack Cheese, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Product Shortage of Advanced Sterilization Products Sterrad Cyclesure 24 Biological Indicator, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Advanced Sterilization Products Sterrad Cyclesure 24 Biological Indicator: FDA Safety Communication - Product Shortage, FDA MedWatch
• Medical Device Safety and Recalls: Fisher and Paykel Healthcare, Ltd., Infant Nasal CPAP Prongs, U.S. Food & Drug Administration (FDA)
• FDA approves Dalvance to treat skin infections, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Thai Soba Noodle Salad in Five States, Due to Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fisher and Paykel Healthcare, Ltd., Infant Nasal CPAP Prongs: Class I Recall - Prongs May Detach from Nasal Tubing and Interrupt Therapy, FDA MedWatch
• Kind Healthy Snacks Issues Allergy Alert Due to Potential Presence of Peanut Protein in Strong and Kind Bars and Kind Healthy Grains Maple Pumpkin Seeds Bars, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - NaturaLyte Liquid Bicarbonate Concentrate: Recall - Potential Health Risk, FDA MedWatch
• FDA MedWatch - Baxter ABACUS TPN Calculation Software: Class I Recall - Software Errors May Cause Toxic/Overdose Symptoms, FDA MedWatch
• FDA MedWatch - Maquet Datascope Intra-Aortic Balloon Pumps: Class I Recall - Failure of Fan Assembly, FDA MedWatch
• Voluntary Nationwide and Canada Recall of NaturaLyte® Liquid Bicarbonate Concentrate Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• FDA targets illegal online pharmacies in globally coordinated action, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Baxter Corporation Englewood, ABACUS Total Parenteral Nutrition Calculation Software, Versions 3.1, 3.0, 2.1, and 2.0, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Maquet Datascope Corporation, Intra-Aortic Balloon Pumps, System 98/98XT, CS100/CS100i, and CS300, U.S. Food & Drug Administration (FDA)
• Sherman Produce Recalls Bulk and Packaged Walnuts Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 21, 2014, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Investigates Outbreak of Human Salmonella Typhimurium Infections Linked to Frozen Feeder Rodents Packaged by Reptile Industries Inc., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA is Vigilant About Keeping Your Pets Safe, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Alaris Pump Module (Model 8100), Version 9.1.18 Software by CareFusion 303, Inc: Class I Recall - May Not Properly Delay an Infusion, FDA MedWatch
• Medical Device Safety and Recalls: CareFusion 303, Inc., Alaris Pump Module (Model 8100), Version 9.1.18 - Software May Not Properly Delay an Infusion with "Delay Until" Option or "Multidose" Feature, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FSMA - Extension of Comment Period for Proposed Rule on Sanitary Transportation of Human and Animal Food, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Get the Facts about Pain Relievers for Pets, U.S. Food & Drug Administration (FDA)
• Middle East Bakery, Inc. Issues Allergy Alert on Undeclared Milk in Market Basket Dairy-free, Gluten-free Pancakes, U.S. Food & Drug Administration (FDA)
• Lansal, Inc. Voluntarily Recalls Hummus & Dip Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Allergy Alert on Undeclared Milk in Pancakes, U.S. Food & Drug Administration (FDA)
• Kraft Foods Group Voluntarily Recalls Select Cottage Cheese Products Due to Out-of-Standard Storage Temperatures, U.S. Food & Drug Administration (FDA)
• WhiteWave Foods Issues Allergy Alert on Undeclared Almondmilk in Half Gallon Silk Light Original Soymilk Containers, U.S. Food & Drug Administration (FDA)
• Áreas naturales para explorar en familia, GobiernoUSA.gov
• CVM Updates - FDA to Retain Current Small Numbers of Animals for Minor Use in Major Species, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Labetalol Hydrochloride Injection 100 MG/20 ML (5MG/ML), 20 ML, Multidose Vial by Hospira: Recall - Visible Particulates, FDA MedWatch
• FDA MedWatch - Ventlab Resuscitator Bags: Recall - Possible Health Risk, FDA MedWatch
• HIV/AIDS Update - Changes to the Trivicay (dolutegravir) product labeling, U.S. Food & Drug Administration (FDA)
• Hospira Announces Voluntary Nationwide Recall Of One Lot Of Labetalol Hydrochloride Injection, USP, 100 MG/20 ML (5MG/ML), 20 ML, Multidose Vial, Due To Visable Particulates, U.S. Food & Drug Administration (FDA)
• Ventlab, LLC. Issues a Nationwide Recall of Ventlab Resuscitator Bags Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - April 2014 Drug Safety Labeling Changes includes 53 products with revisions to Prescribing Information, FDA MedWatch
• CVM Updates - FDA Alerts Horse Owners and Veterinarians About Adverse Events Associated with Certain Unapproved Compounded Drugs in Horses, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Alere INRatio2 PT/INR Professional Test Strips - Results Disagree with the Confirmed PT/INR Reference Test Results Performed by Central Laboratory, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Eszopiclone Containing Sleep Aids: Drug Safety Communication - Can Cause Next-Day Impairment, FDA MedWatch
• FDA MedWatch - Dobutamine Injection (250mg/20mL)/Hospira: Recall - Visible Particulates, FDA MedWatch
• FDA requiring lower starting dose for sleep drug Lunesta, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Bravo® Issues Nationwide Recall of Pet Food for Dogs and Cats, U.S. Food & Drug Administration (FDA)
• Bravo® Issues Nationwide Recall of Pet Food for Dogs and Cats, U.S. Food & Drug Administration (FDA)
• Hospira Announces Voluntary Nationwide Recall Of One Lot Of Dobutamine Injection, USP, 250 MG, 20 ML, Single-Dose Fliptop Vial, Due To Visible Particulates, U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 14, 2014, U.S. Food & Drug Administration (FDA)
• US Trading Company Voluntary Recall of Crushed Chili Powder Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Pradaxa (dabigatran): Drug Safety Communication - Lower Risk for Stroke and Death, but Higher Risk for GI Bleeding Compared to Warfarin, FDA MedWatch
• FDA Office of Women's Health - May e-Update, FDA Office of Women's Health
• Surma Distributors LLC, Issues Alert On Undeclared Sulfites In Haque Brand Golden Raisins, U.S. Food & Drug Administration (FDA)
• Domega Ny International Co Ltd Issues Allergy Alert On Undecleared Eggs In Brilliant Cake With Filling Milk (biscuits), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Revised Guidance for Industry on Statistical Evaluation of Stability Data Available, U.S. Food & Drug Administration (FDA)
• Strong America Limited ISSUES ALLERGY ALERT ON UNDECLARED EGG IN “Golden Smell Hotpot Meat Ball Medley”, U.S. Food & Drug Administration (FDA)
• Stonyfield Extends Voluntary Recall of YoBaby Peach/Pear Yogurt Cup 6-packs to 271 Additional Stores in 6 Western States, U.S. Food & Drug Administration (FDA)
• Domega NY International Co LTD Issues Allergy Alert On Undeclared Peanuts In YF Sesame Flavor Cracker, U.S. Food & Drug Administration (FDA)
• Salud de la mujer: ¿tiene preguntas sobre su cobertura médica?, GobiernoUSA.gov
• Salud de la mujer: ¿tiene preguntas su cobertura médica?, GobiernoUSA.gov
• Datascope Corp/MAQUET Issues Worldwide Voluntary Recall of the System 98/98XT, CS100, CS100i and CS300 Intra-Aortic Balloon Pumps For Potential Mechanical Failure of the Power Supply Fan Assembly, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals May 2014 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Hospira Inc., GemStar Docking Station (List Number 13075) – Potential for Error or Failure to Power Up, U.S. Food & Drug Administration (FDA)
• FDA allows marketing of first prosthetic arm that translates signals from person’s muscles to perform complex tasks, U.S. Food & Drug Administration (FDA)
• STE Fromagere Du Livradois Voluntarily Recalls Raclette Cheese and Montboissie Cheese for Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Zontivity to reduce the risk of heart attacks and stroke in high-risk patients, U.S. Food & Drug Administration (FDA)
• MDA Issues Consumer Advisory for Five Flavors of Lily Bloom’s Kitchen Poparoons Milk Ingredient was Undeclared on Labels, U.S. Food & Drug Administration (FDA)
• Happy Mother's Day! Get FDA Resources for Moms, FDA Office of Women's Health
• Update of CVM's What's New - How are we implementing the FSMA?, U.S. Food & Drug Administration (FDA)
• The May 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 07, 2014, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Safety Communication - Removing Retrievable Inferior Vena Cava Filters, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Alere INRatio2 PT/INR Professional Test Strips: Recall - Higher INR when Performed by Central Laboratory, FDA MedWatch
• Alere Initiates Voluntary URGENT PRODUCT RECALL of Alere INRatio 2 PT/INR Professional Test Strips, U.S. Food & Drug Administration (FDA)
• Eugene Oregon, Inc. Issues Voluntary Nationwide Recall of African Black Ant, Black Ant, and Mojo Risen Dietary Supplements Which May Contain Undeclared Active Pharmaceutical Ingredients, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Approves HALAMID Aqua to Treat Disease in Freshwater Fish, U.S. Food & Drug Administration (FDA)
• Pacific Organic Produce Announce Voluntary Recall of Mangos Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Pacific Organic Produce Announce Voluntary Recall of Mangos Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Sixdog Investments Voluntarily Recalls Eggs Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Changes to the Edurant (rilpivirine) label: drug-drug interaction update, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Hospira Inc., Abbott Acclaim Infusion Pumps and Hospira Acclaim Encore Infusion Pumps - Broken Door Assemblies May Result in Over-Infusion or Delay of Therapy, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listings - Approved Medicated Feed Mill Licenses/Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
• Anhing Corporation Announces a Voluntary Recall of Chili Powder Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Blue Bunny Premium Bordeaux Cherry Chocolate Ice Cream Recalled for Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Abbott Acclaim and Hospira Acclaim Encore Infusion Pumps by Hospira, Inc: Class I Recall - Broken Door Assemblies, FDA MedWatch
• FDA MedWatch - Gemstar Docking Station by Hospira, Inc: Class I Recall - Potential for Error or Failure to Power Up, FDA MedWatch
• Hospira Announces Urgent Nationwide Medical Device Correction For Gemstar Docking Station, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sigma Spectrum Infusion Pumps with Master Drug Library by Baxter Healthcare: Class I Recall - System Error May Interrupt or Delay Therapy, FDA MedWatch
• Update of CVM's What's New - Operational Strategy for Implementing the FDA Food Safety Modernization Act, U.S. Food & Drug Administration (FDA)
• NOH Foods Of Hawaii Issues Allergy Alert On Undeclared Milk In Hawaiian Coconut Pudding Haupia (LUAU Dessert), U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 30, 2014, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update -Revised HHS Adult and Adolescent Antiretroviral Treatment Guidelines available, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Baxter Healthcare Corporation, Sigma Spectrum Infusion Pumps with Master Drug Library Model No. 35700BAX and 35700ABB, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - May 1, 2014, U.S. Food & Drug Administration (FDA)
• Bacai Inc. Issues Voluntary Worldwide Recall of LiteFit USA, U.S. Food & Drug Administration (FDA)
• Two Private Selection Ice Cream Flavors Recalled for Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Flawless Beauty and Skin Products: Recall - Unapproved Drugs, FDA MedWatch
• Flawless Beauty and Skin Issues Voluntary USA Recall of Unapproved Drugs, U.S. Food & Drug Administration (FDA)
• FDA approves Zykadia for late-stage lung cancer, U.S. Food & Drug Administration (FDA)
• Resources for National Women’s Health Week, FDA Office of Women's Health
• FDA MedWatch - GenStrip Blood Glucose Test Strips by Shasta Technologies: FDA Safety Communication - May Report False Results, FDA MedWatch
• FDA MedWatch - HeartWare, Inc., Heartware Ventricular Assist System: Class I Recall - Locking Mechanism of Pump Driveline Connector May Fail to Engage, FDA MedWatch
• Medical Device Safety and Recalls: HeartWare, Inc., Heartware Ventricular Assist System - Locking Mechanism of Pump Driveline Connector May Fail to Engage, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: FDA Safety Communication - Shasta Technologies GenStrip Blood Glucose Test Strips May Report False Results, U.S. Food & Drug Administration (FDA)
• FDA issues proposals to address risks associated with surgical mesh for transvaginal repair of pelvic organ prolapse, U.S. Food & Drug Administration (FDA)
• Medicines in My Home Update: Be Active in Your Health, U.S. Food & Drug Administration (FDA)
• ¿Qué haría si pudiera regalarle a alguien más tiempo?, GobiernoUSA.gov
• FDA MedWatch - Super Arthgold by Nano Well-being Health: Recall - Undeclared Drug Ingredients, FDA MedWatch
• Stonyfield Announces Voluntary Recall of 188 6-packs of Yobaby Peach/Pear Yogurt Cups from 40 Target Stores in the Southeast and 82 Mid-Atlantic Walmart Stores, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Questions and Answers for Brewers/Distillers on the FSMA Proposed Rule for Preventive Controls for Animal Food, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Voice - Getting it Right on Spent Grains, U.S. Food & Drug Administration (FDA)
• FDA approves first human papillomavirus test for primary cervical cancer screening, FDA Office of Women's Health
  • <Possible follow-ups>
  • FDA approves first human papillomavirus test for primary cervical cancer screening, U.S. Food & Drug Administration (FDA)
• FDA proposes to extend its tobacco authority to additional tobacco products, including e-cigarettes, U.S. Food & Drug Administration (FDA)
• Nano Well-being Health Inc. Issues Voluntary Nationwide Recall of Super Arthgold Due to Undeclared Ingredients, U.S. Food & Drug Administration (FDA)
• Miravalle Foods, Inc. Recalls Ground Annato Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 23, 2014, U.S. Food & Drug Administration (FDA)
• FDA approves Sylvant for rare Castleman's disease, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Epidural Corticosteroid Injection: Drug Safety Communication - Risk of Rare But Serious Neurologic Problems, FDA MedWatch
• Hospira Announces Voluntary Nationwide Recall of One Lot of 0.25% Marcaine™ (Bupivacaine HCI Injection, USP), 10 ml, Single-Dose, Preservative-Free Vial Due to Visible Particulates, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Marcaine (Bupivacaine HCI Injection, USP) 0.25 percent, 10 ml, Single-Dose, Preservative-Free Vial: Recall - Visible Particulates, FDA MedWatch
• Hospira Announces Voluntary Nationwide Recall of One Lot of 0.25% Marcaine&trade; (Bupivacaine HCI Injection, USP), 10 ml, Single-Dose, Preservative-Free Vial Due to Visible Particulates, U.S. Food & Drug Administration (FDA)
• Dominex Natural Foods, LLC, Issues Voluntary Recall Due to Possible Undeclared Nut Allergen in AngelBowls brand of Corkscrew Pasta & Creamy Tomato Vodka Sauce Pasta Bowl, U.S. Food & Drug Administration (FDA)
• FDA proposes new expedited access program for medical devices that address unmet medical needs, U.S. Food & Drug Administration (FDA)
• Wegmans Food Markets, Inc. Issues Allergy Alert on Undeclared Egg in Wegmans Easter Bread, 17 oz., U.S. Food & Drug Administration (FDA)
• FDA approves Cyramza for stomach cancer, U.S. Food & Drug Administration (FDA)
• Beneficios del Gobierno para personas con discapacidades, GobiernoUSA.gov
• Medical Device Safety and Recalls: Covidien, Pipeline Embolization Device and Alligator Retrieval Device - (Certain Catalog / Lot Numbers) - Coating on Delivery Wire Could Delaminate and Detach, U.S. Food & Drug Administration (FDA)
• Cómo obtener el estado de su reembolso de impuestos, GobiernoUSA.gov
• Hickory Farms Issues Allergy Alert on Chipotle Ranch Sauce Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Southwest Region Recalls Mini Butter Croissants Due to Undeclared Egg, U.S. Food & Drug Administration (FDA)
• Hospira Announces Voluntary Nationwide Recall of One Lot of 1% Lidocaine HCI INjection, USP, Due To Visible Particulates, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lidocaine HCI Injection, USP, by Hospira: Recall - Visible Particulates, FDA MedWatch
• FDA MedWatch - CUBICIN (daptomycin for injection) by Cubist Pharmaceuticals: Recall - Presence of Particulate Matter, FDA MedWatch
• FDA MedWatch - Propofol Injectable Emulsion, USP by Hospira: Recall - Visible Particulates, FDA MedWatch
• Nature’s Universe Issues Voluntary Worldwide Recall of All Thinogenics Products Sold Prior to 02/06/2014 Due to the Presence of Undeclared Sibutramine, U.S. Food & Drug Administration (FDA)
• Hospira Announces Nationwide Voluntary Recall of Seven Lots of Propofol Injectable Emulsion, USP, Due to Visible Particulates, U.S. Food & Drug Administration (FDA)
• Price Chopper Supermarkets Recalls Price Chopper Brand Tuscan White Bean Hummus due to Mislabeling, U.S. Food & Drug Administration (FDA)
• FDA approves Ragwitek for short ragweed pollen allergies, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Laparoscopic Power Morcellation in Hysterectomy and Myomectomy: FDA Safety Communication - Use Discouraged Due to Increased Risk in Women With Uterine Fibroids, FDA MedWatch
• Medical Device Safety and Recalls: Spacelabs Healthcare Ltd., ARKON Anesthesia Delivery System with Version 2.0 Software - Software Defect May Cause System to Stop Working, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Laparoscopic Uterine Power Morcellation in Hysterectomy and Myomectomy - FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Marsha Henderson Leads Programs to Improve Health Outcomes for Women, FDA Office of Women's Health
• FDA MedWatch - ARKON Anesthesia Delivery System with Version 2.0 Software by Spacelabs Healthcare: Class I Recall, FDA MedWatch
• Update of CVM's What's New - New Brochure Available - Pet Turtles: A Source of Germs, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Purina Animal Nutrition LLC Recalls Poultry Feeds Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Natural Organics, Inc. Recalls one lot ofTHURSDAY PLANTATION TEA TREE MOUTHWASH Due to Bacterial Contamination, U.S. Food & Drug Administration (FDA)
• Health Matters America Inc. Issues Allergy Alert on Undeclared Milk in Organic Traditions Brand Dark Chocolate Golden Berries and Dark Chocolate Sacha Inchi Seeds, U.S. Food & Drug Administration (FDA)
• Purina Animal Nutrition LLC Recalls Poultry Feeds Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 16, 2014, U.S. Food & Drug Administration (FDA)
• Cómo ahorrar y cuidar su dinero: publicaciones para usted, GobiernoUSA.gov
• Proteja a su bebé con las vacunas, GobiernoUSA.gov
• Update of CVM's What's New - Keep Lilies Away From Your Cats, U.S. Food & Drug Administration (FDA)
• Private Selection Sweet Strawberry Sorbet Recalled for Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• La Compañía Fernández Chile Inc. retira del mercado Chile Molido Puro de 4 onzas y Chile Rojo de 6 onzas por contaminación potencial de Salmonella, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 09, 2014, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Covidien Pipeline Embolization Device and Alligator Retrieval Device: Recall - Coating on Delivery Wire Could Delaminate, FDA MedWatch
• Covidien Implements Voluntary Recall of its Pipeline&trade; Embolization Device and Alligator&trade; Retrieval Device, U.S. Food & Drug Administration (FDA)
• Sinco Inc Issues Allergy alert on undeclared Peanut Protein in Archer Farms Chocolate Hazelnut Swirl Gelato, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Abbott Diabetes Care, Inc. FreeStyle and FreeStyle Flash Blood Glucose Meters including the FreeStyle Blood Glucose Meter built into the OmniPod Personal Diabetes Manager (PDM), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - March 2014 Drug Safety Labeling Changes includes 30 products with revisions to Prescribing Information, FDA MedWatch
• Fernandez Chile Company Inc. Recalls 4oz Chile Molido Puro and 6oz Chile Rojo Potential Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA approves expanded indication for certain pacemakers and defibrillators, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Labeling update for Isentress (raltegravir), U.S. Food & Drug Administration (FDA)
• FDA Women's Health Highlights: April e-Update, FDA Office of Women's Health
• Swanson Health Products Recalls Full Spectrum Cilantro, U.S. Food & Drug Administration (FDA)
• Bissinger’s Announces a Voluntary Recall of Its Dark Chocolate Bunny Ears Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Su declaración de impuestos: sugerencias para el último minuto, GobiernoUSA.gov
• Update of CVM's What's New - The Robert Abady Dog Food Co., LLC Recalls "Abady Highest Quality Maintenance & Growth Formula for Cats", U.S. Food & Drug Administration (FDA)
• Lisy Corporation Issues Recall on: Lisy Sweet Basil (Albahaca) 6 Oz., Item 1132 Lot #'s A013 0518 & A014 0518, U.S. Food & Drug Administration (FDA)
• The Robert Abady Dog Food Co., LLC Recalls "Abady Highest Quality Maintenance & Growth Formula for Cats" Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Frontier Natural Products Co-op Initiates Voluntary Class 1 Recall Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Changes to the Prezista (darunavir) label, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Voluntary Withdrawal of 19 Antimicrobials for Use in Food-Producing Animals, U.S. Food & Drug Administration (FDA)
• Buffalo Sav Inc. Issues Allergy Alert On Undeclared Soy In “Grandma's Perogies Potato & Bacon Perogies”, U.S. Food & Drug Administration (FDA)
• The April 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• OWH Director receives Women's Health Leadership Award, FDA Office of Women's Health
• Update of CVM's What's New - Updated MUMS Drug Designations List/Veterinary Master Files, U.S. Food & Drug Administration (FDA)
• Frontier Natural Products Co-op Initiates Voluntary Class 1 Recall Due to Possible Health Risk from Organic Black Peppercorns, U.S. Food & Drug Administration (FDA)
• Sprouts Farmers Market Recalls Organic Black Peppercorns Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Whole Foods Market’s Northern California Region Recalls Chipotle Chicken Wraps Due to Undeclared Fish Allergen, U.S. Food & Drug Administration (FDA)
• Publicaciones gratis para manejar mejor su dinero, GobiernoUSA.gov
• Asegure la educación de sus hijos con los planes 529, GobiernoUSA.gov
• Emparedados Boricua Emite Una Alerta Por Al&eacute;rgenos En Sus Productos “Emparedados Boricua – Pollo y Queso”, U.S. Food & Drug Administration (FDA)
• Koru Pacific Packaging Announces a Voluntary Recall for One Lot # AH!LASKA&reg; Organic Cocoa Non-Dairy Chocolate Mix, 12 oz. Canister Due to Possible Milk Allergen, U.S. Food & Drug Administration (FDA)
• Natural Organics, Inc. Recalls One Lot of THURSDAY PLANTATION TEA TREE MOUTHWASH Due to Bacterial Contamination, U.S. Food & Drug Administration (FDA)
• Emparedados Boricua Issues Allergen Alert For Its Products "Emparedados Boricua - Chicken and Cheese", U.S. Food & Drug Administration (FDA)
• Proposed health IT strategy aims to promote innovation, protect patients, and avoid regulatory duplication, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Dräger Medical Inc., Evita V500 and Babylog VN500 Ventilators with Optional PS500 Power Supply Units - Battery Depletion, U.S. Food & Drug Administration (FDA)
• FDA Commissioner Margaret A. Hamburg Statement on Prescription Opioid Abuse, U.S. Food & Drug Administration (FDA)
• FDA approves new hand-held auto-injector to reverse opioid overdose, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FSMA and Animal Feed - Final Rule and Guidance on Record Access Requirements, U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 02, 2014, U.S. Food & Drug Administration (FDA)
• Nuevos datos sobre el autismo revelan aumento en casos detectados, GobiernoUSA.gov
• FDA MedWatch - PS500 Power Supply Unit by Dräger: Recall - Early Depletion of Battery Charge, FDA MedWatch
• Dräger Issues Voluntary Nationwide Recall of Optional PS500 Power Supply for Evita V500 and Babylog VN500 Ventilators, U.S. Food & Drug Administration (FDA)
• FDA approves first sublingual allergen extract for the treatment of certain grass pollen allergies, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals April 2014 Update, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Thoratec Corporation, HeartMate II LVAS Pocket System Controller – Insufficient Labeling and Training for Patients Switched from the EPC Controller, U.S. Food & Drug Administration (FDA)
• Lao Thai Nam Corp. Voluntarily Recalls Number One Sompa Salted Fish, Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Revatio (sildenafil): Drug Safety Communication - FDA Clarifies Warning About Pediatric Use for Pulmonary Arterial Hypertension, FDA MedWatch
• Vita Food Products Issues Voluntary Recall of ELF Herring Fillets in Wine Sauce Containing Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Nova Products, Inc. Issues Voluntary Nationwide Recall of Dietary Supplements with Undeclared Active Pharmaceutical Ingredients, U.S. Food & Drug Administration (FDA)
• Fresh Express Issues Recall of Limited Quantity of Already Expired Italian Salad Due to Possible Health Risk, No Illnesses Cited, U.S. Food & Drug Administration (FDA)
• FDA approves first long-acting recombinant coagulation Factor IX concentrate for patients with Hemophilia B, U.S. Food & Drug Administration (FDA)
• FDA approves Topamax for migraine prevention in adolescents, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Alli (60 mg orlistat capsules) by GlaxoSmithKline: Recall - Product Tampering, FDA MedWatch
• Glaxosmithkline Recalls Alli&reg;, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Announces Availability of Draft Guidance on Prior Notice of Imported Foods, U.S. Food & Drug Administration (FDA)
• Macadamia Nut Allergy Alert and Voluntary Recall of 15-Count Boxes of Chocolate Chunk LUNA Bars Due to Package Mislabeling, U.S. Food & Drug Administration (FDA)
• BBM Chocolate Distributors, Ltd. Issues Allergy Alert on Undeclared Milk in "CHOCOLAT Alprose 52% CACAO PREMIUM DARK CHOCOLATE, Alprose Swiss Chocolate Dark Chocolate and CHOCOLAT Alprose NAPOLITAINS SWITZERLAND”, U.S. Food & Drug Administration (FDA)
• Vermont Common Foods Issues Allergy Alert on Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• Oscar’s Smokehouse, Inc. Recalls “Eleven Varieties (11) Of Cheese Spreads” Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 26, 2014, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Receives Strong Industry Commitment for its Antibiotic Resistance Strategy, U.S. Food & Drug Administration (FDA)
• Pure Edge Nutrition, LLC Issues Voluntary Nationwide Recall of Bella Vi Brand Products Due to Undeclared Sibutramine and Phenolphthalein, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Partners With Veterinary Labs to Help Animals, U.S. Food & Drug Administration (FDA)
• New Life Nutritional Center Issues Voluntary Nationwide Recall of Super Fat Burner, Maxi Gold and Esmeralda Dietary Supplements Due to the Presence of Undeclared Sibutramine and Phenolphthalein, U.S. Food & Drug Administration (FDA)
• Parkers Farm Acquisition, LLC Issues Voluntary Recall of Products Due to Listeria Contamination, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Baraclude (entecavir) label revised to expand pediatric indication, U.S. Food & Drug Administration (FDA)
• FDA approves Otezla to treat psoriatic arthritis, U.S. Food & Drug Administration (FDA)
• Helados La Tapatia, Inc. Retira Productos Debido a un Posible Riesgo de Salud, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Pleo Homeopathic Drug Products by Terra-Medica: Recall - Potential for Undeclared Penicillin, FDA MedWatch
• FDA approves first implantable hearing device for adults with a certain kind of hearing loss, U.S. Food & Drug Administration (FDA)
• Terra-Medica Issues Voluntary Nationwide Recall of Specified Lots of Pleo Homeopathic Drug Products Due to the Potential for Undeclared Penicillin, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces New Reporting Tool for Livestock Animal Food Problems, U.S. Food & Drug Administration (FDA)
• Helados La Tapatia, Inc. Recalls Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 19, 2014, U.S. Food & Drug Administration (FDA)
• Mercado de Seguros Médicos: cierre del plazo de inscripción, GobiernoUSA.gov
• FDA approves Impavido to treat tropical disease leishmaniasis, U.S. Food & Drug Administration (FDA)
• Harry’s Farmers Market Recalls Amberjack From One Store in Marietta, GA. Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Update on Proposed Rules under the FDA Food Safety Modernization Act, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - February 2014 Drug Safety Labeling Changes includes 35 products with revisions to Prescribing Information, FDA MedWatch
• Elija el mejor plan de seguro médico para usted y su familia, GobiernoUSA.gov
• March 21 Registration Deadline for Presenters at FDASIA 907 Public Hearing, FDA Office of Women's Health
• CVM Updates - FDA Approves First Insulin Product for Use with Automatic Injection Pen in Cats and Dogs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Playtex Nurser Deluxe Double Electric Breast Pump: Recall - Potential for Electric Shock, FDA MedWatch
• Playtex Announces the Voluntary Nationwide Recall of Certain AC/DC Power Adapters Used With the Playtex® Nurser Deluxe Double Electric Breast Pump Due to Potential for Electric Shock, U.S. Food & Drug Administration (FDA)
• Hospira Announces Voluntary Nationwide Recall of Hemoset Blood Set, U.S. Food & Drug Administration (FDA)
• Cómo planificar un viaje en auto para toda la familia, GobiernoUSA.gov
• Fannie May Issues a Voluntary Recall of 89.08 Cases of 14.0 oz. Spring Wrapped Assorted Chocolate Box Due to Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of atazanavir sulfate and ritonavir Fixed-Dose Combination tablets, U.S. Food & Drug Administration (FDA)
• Fannie May Issues A Voluntary Recall of 19 Boxes of 14.0 Oz. Spring Wrapped Assorted Chocolate Box Due to Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• Simply Natural Foods, Llc Issues Allergy Alert For high Levels Of Milk Protein In Simply Lite Dark Chocolate Bars, U.S. Food & Drug Administration (FDA)
• Some lots of Simply Lite brand dark chocolate recalled, U.S. Food & Drug Administration (FDA)
• Infinite Herbs, LLC Voluntarily Recalls One Lot of Basil Organic Clamshells Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval: lamivudine and tenofovir disoproxil fumarate FDC tablets with nevirapine, U.S. Food & Drug Administration (FDA)
• Abbott Issues Recall of Certain Blood Glucose Monitoring Systems, U.S. Food & Drug Administration (FDA)
• SNI National is Voluntarily recalling Kratom XL 4 Pack, Maeng Da Kratom 10 Pack, Max Kratom 20 Pack, and Bali Kratom 40 pack Due to Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - FreeStyle and FreeStyle Flash Blood Glucose Meter by Abbott: Recall - May Produce Mistakenly Low Blood Glucose Results, FDA MedWatch
• Medical Device Safety and Recalls: McKesson Technologies, McKesson Anesthesia Care – Patient Case Data May Not Match Patient Data, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - VPRIV (velaglucerase alfa for injection): Recall - Visible Particulate Matter, FDA MedWatch
• FDA MedWatch - Merit Medical Systems, Custom Procedural Trays/Kits Containing 1 percent Lidocaine HCl Injection, 10mg/mL: Recall - Particulates Found in Hospira supplied Lidocaine, FDA MedWatch
• FDA MedWatch - Reumofan Plus: Recall - Undeclared Drug Ingredient [UPDATE], FDA MedWatch
• La Compania Pain Free by Nature Retira del Mercado las Tabletas de Reumofan Plus Debido a Ingredientes Medicos no Declarados, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • La Compania Pain Free by Nature Retira del Mercado las Tabletas de Reumofan Plus Debido a Ingredientes Medicos no Declarados, U.S. Food & Drug Administration (FDA)
• Shire Pharmaceuticals Initiates Voluntary Nationwide Recall of One Batch, Packaged into Three Lots, of VPRIV® (velaglucerase alfa for injection), U.S. Food & Drug Administration (FDA)
• Dole Fresh Vegetables Voluntarily Recalls Limited Number of Bagged Salads Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Amends Regulations for Disclosure of New Animal Drug Approvals to Improve Timeliness of Public Disclosure, U.S. Food & Drug Administration (FDA)
• Kirkland Signature Real Sliced Fruit Recalled Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Merit Medical Systems, Custom Procedural Trays/Kits Containing 1% Lidocaine HCl Injection, USP, 10mg/mL - Particulates Found in Hospira supplied 1% Lidocaine HCl, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Greatbatch Medical, Offset Cup Impactor - Inadequate Sterilization, U.S. Food & Drug Administration (FDA)
• Pain Free by Nature is Voluntarily Recalling Reumofan Plus Tablets Due to Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 12, 2014, U.S. Food & Drug Administration (FDA)
• Cambio de hora - 9 de marzo, GobiernoUSA.gov
• The March 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Philips Respironics, Trilogy Ventilator, Models 100, 200, and 202 - Failure to Deliver Mechanical Breaths, U.S. Food & Drug Administration (FDA)
• Hong Lee Trading Inc. Issues an Alert on Undeclared Sulfites in “Mut Dua Non” Young Coconut Candy (Strips), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Effexor XR 150 Mg Extended-Release Capsules (Pfizer) and Venlafaxine HCl 150 Mg Extended-Release Capsules (Greenstone): Recall - Possible Presence of Tikosyn Capsules, FDA MedWatch
• Net Food Brand Turkey Dried Apricots Recalled Because of Undeclared Sulfites, U.S. Food & Drug Administration (FDA)
• Pfizer Initiates Nationwide Voluntary Recall of Two Lots of Pfizer’s Effexor XR® 150 Mg Extended-Release Capsules and One Lot of Greenstone’s Venlafaxine HCl 150 Mg Extended-Release Capsules Due to the Possible Presence of Tikosyn® Capsules, U.S. Food & Drug Administration (FDA)
• Crown Food Distributors, Inc. Issues Allergy Alert on Undeclared Sulfites and Undeclared Yellow #6 in Golden Natural Fruit Island, U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 05, 2014, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Doribax (doripenem): Drug Safety Communication - Risk When Used to Treat Pneumonia on Ventilated Patients, FDA MedWatch
• FDA MedWatch - DIANEAL PD-2 Peritoneal Dialysis Solution with 1.5 Percent Dextrose 6000mL: Recall - Contamination With Mold, FDA MedWatch
• FDA Office of Women's Health March e-Update, FDA Office of Women's Health
• Gretchen’s Shoebox Express Issues Allergy Alert for Limited Number of Greek Yogurt Raspberry & Lemon Parfait cups Due to Undeclared Eggs., U.S. Food & Drug Administration (FDA)
• Baxter Initiates U.S. Voluntary Recall of One Lot of Peritoneal Dialysis Solution Due to Container-Closure Non-Integrity, U.S. Food & Drug Administration (FDA)
• House of Flavors Issues Voluntary Recall Due to Possible Undeclared Nut Allergen in Belmont Chocolate Chip Cookie Dough Ice Cream, U.S. Food & Drug Administration (FDA)
• Acceda a servicios del Gobierno, GobiernoUSA.gov
• Plum Organics Voluntarily Recalls Limited Quantity of Two Varieties of World Baby Pouch Products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HeartMate II LVAS Pocket System Controller by Thoratec Corporation: Medical Device Correction - Updated Labeling and Training Materials, FDA MedWatch
• Twin Marquis, Inc Issues Allergy Alert on Undeclared Milk in Specific Lots of its Cooked Noodle and Lo Mein Noodle, U.S. Food & Drug Administration (FDA)
• Thoratec Corporation Issues Worldwide Urgent Medical Device Correction Letter to Update its Labeling Regarding the Use of the HeartMate II® LVAS Pocket System Controller, U.S. Food & Drug Administration (FDA)
• Lehigh Valley Dairy Conducts Voluntary Recall of Lehigh Valley, Swiss Premium, and Price Chopper Brand Orange Juice Because It May Contain Undeclared Allergen (Milk), U.S. Food & Drug Administration (FDA)
• ACTUALIZACIÓN (RETIRO EXTENDIDO) La compañía Roos Foods retira del mercado voluntariamente una variedad de quesos (enlistados abajo) debido a un posible riesgo sanitario, U.S. Food & Drug Administration (FDA)
• HC Schau and Sons issues allergy alert on undeclared Pine Nuts in ‘Fresh To Go’ Tuscan Style Combo on Tomato Basil Bread (sandwich)., U.S. Food & Drug Administration (FDA)
• Plum Organics Voluntarily Recalls Limited Quanity of Two Varieties of World Baby Pouch Products, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals March 2014 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Conozca la diferencia entre la validez de su visa y el tiempo de estadía autorizado, GobiernoUSA.gov
• Unilever United States, Inc. Issues Allergy Alert for Limited Number of 20-Count Boxes of Popsicle Orange, Cherry and Grape Ice Pops Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Jinsunmi International Inc. Issues A Voluntary Recall Of Its 17.98 oz Lotte Brand Frozen Fruit Bar (watermelon flavor) Due To Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• Mars Food North America Voluntarily Recalls Specific Batch and Item Number Representing Less Than 3,500 Cases, U.S. Food & Drug Administration (FDA)
• (UPDATE) EXPANDED - Roos Foods Voluntarily Recalls Variety of Cheeses (listed below) Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Resuscitation Systems with Oxygen and Air inlet Fittings Reversed During Assembly, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GE Healthcare Resuscitation Systems: Class I Recall - Oxygen and Air Inlet Fittings Reversed During Assembly, FDA MedWatch
• Update of CVM's What's New - CVM Feed Sampling Survey Assignments, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces New Program for State Animal Feed Regulators, U.S. Food & Drug Administration (FDA)
• GobiernoUSA.gov en Twitter, GobiernoUSA.gov
• FDA proposes updates to Nutrition Facts label on food packages, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 26, 2014, U.S. Food & Drug Administration (FDA)
• Investigan quesos contaminados de gran consumo hispano, GobiernoUSA.gov
• Medicines in My Home Update - American Heart Month reminder: Ask your doctor before taking daily aspirin, U.S. Food & Drug Administration (FDA)
• Haga sus trámites fácilmente y en español, GobiernoUSA.gov
• Update of CVM's What's New - Paperwork Reduction Act Notices webpage available, U.S. Food & Drug Administration (FDA)
• EXPANDIDO - La Compania Roos Foods Retira del Mercado Voluntariamente una Variedad de Quesos (Enlistados Abajo) Debido a un Posible Riesgo Sanitario, U.S. Food & Drug Administration (FDA)
• EXPANDED - Roos Foods Voluntarily Recalls Variety of Cheeses (listed below) Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Changes to the Victrelis (boceprevir) label, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - ACME Monaco Guidewire .035x150 3MMJ TCFC, Item 88241 by Medline Industries: Class I Recall - Potential for Coating to Flake Off, FDA MedWatch
• Medical Device Safety and Recalls: Medline Industries – ACME Monaco Guidewire .035x150 3MMJ TCFC, Item 88241, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Video Available - Pet Food and Treats in Your Home, U.S. Food & Drug Administration (FDA)
• FDA approves Myalept to treat rare metabolic disease, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Teleflex Medical, ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port - Potential Kinking During Patient Use, U.S. Food & Drug Administration (FDA)
• La Compania Roos Foods Retira del Mercado Voluntariamente Una Variedad de Quesos (Enlistados Abajo) Debido a un Posible Riesgo Sanitario, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port (with and without Preloaded Stylet) by Teleflex Medical – Class I Recall: Potential Kinking During Patient Use, FDA MedWatch
• Wolfgang B. Gourmet Foods, Inc. Issues Allergy Alert on Undeclared Fish (Anchovies) in Two Lots Of Fairway Brand Condiment Grilling Sauce, U.S. Food & Drug Administration (FDA)
• Roos Foods Voluntarily Recalls Variety of Cheeses Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Evolution Fresh Voluntarily Recalls Select Bottles of “Organic Sweet Greens and Ginger” Juice Sold at California and Nevada Grocery Retailers, U.S. Food & Drug Administration (FDA)
• FDA issues first orders to stop sale, distribution of tobacco products, U.S. Food & Drug Administration (FDA)
• Updated - Fannie May Issues A Voluntary Recall Of Its 4.0 Oz. Heart-shaped Box Of Assorted Chocolates Due To Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• Falafel King Voluntarily Recalls Hatch Green Chile Hummus and Hatch Green Chile Wraps Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 19, 2014, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Etomidate Injection/Pfizer-Mylan: Recall - Presence of Particulate Matter and/or Illegible and Missing Lot Number and/or Expiry Date, FDA MedWatch
• Update of CVM's What's New - Med-Vet International Issues Nationwide Recall of Veterinary 1/2cc U-40 Insulin Syringes Due to Mismarked Syringe Barrels, U.S. Food & Drug Administration (FDA)
• Med-Vet International Issues Nationwide Recall of Veterinary 1/2cc U-40 Insulin Syringes Due to Mismarked Syringe Barrels, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Mid-Atlantic Region Recalls Tom Yom Soup Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Trilogy Ventilator Models 100, 200 and 202 by Philips Respironics: Recall - Failure to Deliver Mechanical Breaths, FDA MedWatch
• Fannie May Issues A Voluntary Recall Of Its 4.0 Oz. Heart-shaped Box Of Assorted Chocolates Due To Undeclared Peanuts, U.S. Food & Drug Administration (FDA)
• Agila Specialties Private Limited Initiates Voluntary Nationwide Recall of 10 Lots of Etomidate Injection 2 mg/mL – 10 mL and 20 mL due to the Presence of Particulate Matter and/or Illegible and Missing Lot Number and/or Expiry Date, U.S. Food & Drug Administration (FDA)
• Philips Respironics Initiates Recall of Trilogy Ventilator, U.S. Food & Drug Administration (FDA)
• FDA and European Medicines Agency strengthen collaboration in pharmacovigilance area, U.S. Food & Drug Administration (FDA)
• FDA approves Northera to treat neurogenic orthostatic hypotension, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Seeking Public Input on Animal Generic Drug User Fee Act Information Collection, U.S. Food & Drug Administration (FDA)
• 3 temas populares sobre la jubilación, GobiernoUSA.gov
• Update of CVM's What's New - 2014 Windows to Regulatory Research Internship Program – Now Accepting Applications, U.S. Food & Drug Administration (FDA)
• Ice Cream Specialties Issues Allergy Alert On Undeclared Peanut Allergen In Dairy Rich Chocolate Ice Cream, U.S. Food & Drug Administration (FDA)
• MyNicKnaxs, LLC. Issues a Voluntary Nationwide and International Recall of All weight loss formulas of: Magic Slim, Fruta Bio, SlimEasy, Super Fat Burning Bomb, Slim Xtreme, Meizi Evolution, Meizitang Strong Version Botanical Slimming, Jianfeijindan Activity Girl, and Japan Hokkaido Cangye Phamacy Co., LTD Japanese Chinese Formula pill for weight reduction., U.S. Food & Drug Administration (FDA)
• Ben Venue Laboratories, Inc. Issues A Voluntary Nationwide Patient Level Recall Of Acetylcysteine Solution 10%, Usp, Lot 2005479, U.S. Food & Drug Administration (FDA)
• Kettle Brand Voluntarily Recalls Limited Run of Bakes Sea Salt Potato Chips Due to Potential Milk Allergen, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 12, 2014, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Acetylcysteine Solution 10 Percent: Recall - Glass Particles in Product, FDA MedWatch
• FDA MedWatch - L-citrulline by Medisca: UPDATE - Additional Lot Numbers Recalled, FDA MedWatch
• Su corazón es lo primero este día de San Valentín, GobiernoUSA.gov
  • <Possible follow-ups>
  • Su corazón es lo primero este día de San Valentín, GobiernoUSA.gov
• FDA MedWatch - L-citrulline by Medisca: Alert - Potentially Subpotent Product, FDA MedWatch
• MyNicKnaxs, LLC. Issues a Voluntary Nationwide and International Recall of All Weight Loss Formulas of Reduce Weight Fruta Planta, U.S. Food & Drug Administration (FDA)
• Illegal prescription drug sellers arraigned on charges for smuggling illicit cancer drugs into the United States, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FSMA Public Meeting: Proposed Rule on Sanitary Transportation of Human and Animal Food, U.S. Food & Drug Administration (FDA)
• Tandem Diabetes Care Expands Voluntary Recall for Select Lots of Insulin Cartridges Used with t:slim Insulin Pump, U.S. Food & Drug Administration (FDA)
• Roth Farms Recalls "Curly Parsley" Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Label update for Victrelis (boceprevir), U.S. Food & Drug Administration (FDA)
• FDA approves Imbruvica to treat chronic lymphocytic leukemia, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - January 2014 Drug Safety Labeling Changes includes 23 products with revisions to Prescribing Information, FDA MedWatch
• Mars Foodservices US Recalls Infused Rice Products Sold For Wholesale Distribution --UNCLE BEN’S® Retail Grocery Products Not Affected--, U.S. Food & Drug Administration (FDA)
• FDA warns against using Uncle Ben’s Infused Rice, U.S. Food & Drug Administration (FDA)
• Big Red Tomato Packers, LLC Voluntarily Recalls Fresh Tomatoes Due to Possible Risk of Contamination from Salmonella, U.S. Food & Drug Administration (FDA)
• Natural Grocers by Vitamin Cottage Issues Allergy Alert on Undeclared Peanuts in Dark Chocolate Almonds, U.S. Food & Drug Administration (FDA)
• The February 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA Office of Women's Health February e-Update, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Calcium gluconate 10 percent Injections by Rx Formulations: Recall - Microbial Contamination, FDA MedWatch
• Update of CVM's What's New - FY 2013 ADUFA/AGDUFA Performance Reports Available, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Medicated Feed Mill Licenses/Veterinary Feed Directive Distributor Notications, U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 05, 2014, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Pro-Pet LLC Recalls a Limited Number of Dry Dog and Cat Foods Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Pro-Pet LLC Recalls a Limited Number of Dry Dog and Cat Foods Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA Commissioner Hamburg travels to India, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - 2014 Windows to Regulatory Research Internship Program, U.S. Food & Drug Administration (FDA)
• K-Fat Inc. Issues an Alert on Undeclared Sulfites In Kfi Sweetened Ginger Cand, U.S. Food & Drug Administration (FDA)
• Humei Trading Inc. Issues Alert on Undeclared Sulfites in "Dried Lily", U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals February 2014 Update, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update -Approval of generic version of lamivudine and zidovudine tablets, 150 mg/300 mg, U.S. Food & Drug Administration (FDA)
• Cuide su corazón, GobiernoUSA.gov
• HIV/AIDS Update -Tentative approval of atazanavir sulfate capsules, 100 mg, 150 mg, 200 mg, and 300 mg, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Update to Food Safety Modernization Act and Animal Feed, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - February 3, 2014, U.S. Food & Drug Administration (FDA)
• UPDATE: Unified Grocers, Inc. Issues Allergy Alert on Undeclared Eggs in “Special Value Ginger Snap Cookies”, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Testosterone Products: Drug Safety Communication - FDA Investigating Risk of Cardiovascular Events, FDA MedWatch
• FDA Approves Hetlioz: first treatment for non-24 hour sleep-wake disorder in blind individuals, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Approved Animal Drug Products Online (Green Book), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Proposed Rule on Sanitary Transportation of Human and Animal Food, U.S. Food & Drug Administration (FDA)
• Donar sangre es donar vida, GobiernoUSA.gov
• Parents can keep kids safe by talking about misusing prescription medications, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FSMA and Animal Feed - Comment Period Extensions, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Seeking Public Input on Animal Drug User Fee Act Information Collection, U.S. Food & Drug Administration (FDA)
• YoungYou International Issues Voluntary Recall of Mega Slim Herbal Appetite Management Pills Due to Presence of DMAA, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Codman Neuro, TRUFILL n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System - Incorrect Instructions for Use, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 29, 2014, U.S. Food & Drug Administration (FDA)
• Gano Excel USA Inc. Announces Recall of C’Real Spirulina, U.S. Food & Drug Administration (FDA)
• ¿Tiene dudas sobre sus beneficios del Seguro Social?, GobiernoUSA.gov
• Pringles Issues Allergy Alert and Voluntary Recall of One Hour’s Worth of Production of Original Crisps Due to Undeclared Milk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Annual Report to Congress on the Use of Mandatory Recall Authority Available, U.S. Food & Drug Administration (FDA)
• ¿Ya recibió los papeles para preparar sus impuestos?, GobiernoUSA.gov
• Expertos de la Administración del Seguro Social responden preguntas del público, GobiernoUSA.gov
• Update of CVM's What's New - PMI Nutrition, LLC Recalls Red Flannel Cat Food Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Winn-Dixie Recalls Instant Chocolate Drink Mix Sold in Florida, U.S. Food & Drug Administration (FDA)
• PMI Nutrition, LLC Recalls Red Flannel® Cat Food Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Araya Inc. Issues Allergy Alert on Undeclared Tree Nuts, Wheat, Milk and Soy in Their Chocolate Bars, Marshmallows, Dry Fruits and Chocolate Gift Boxes, U.S. Food & Drug Administration (FDA)
• UPDATED: Allergy Allert - Undeclared Milk in Five Kinnikinnick Foods Products, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 22, 2014, U.S. Food & Drug Administration (FDA)
• Cómo evitar a los estafadores y las llamadas de telemercadeo, GobiernoUSA.gov
• Lochiel Enterprises Limited Recalls St Mary’s River Smokehouses Oven Smoked Salmon Stix, Chili Mango Flavor Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Flat Creek Farm & Dairy Recalls Cheese Because of Possible Health Risk Update to Correcy Lot Number Information, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Trufill n-BCA Liquid Embolic System by Codman Neuro: Recall - Incorrect Instructions For Use, FDA MedWatch
• FDA Hepatitis Update - Victrelis (boceprevir) label changes update contraindications and drug interactions, U.S. Food & Drug Administration (FDA)
• FDA Classifies Worldwide Voluntary Correction Notice on TRUFILL® n-BCA Liquid Embolic System as Class I Recall, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Guidances Under Development for 2014, U.S. Food & Drug Administration (FDA)
• FDA launches advisory committee membership nomination portal, U.S. Food & Drug Administration (FDA)
• Rise’N Roll Bakery Issues Allergy Alert on Undeclared Egg in All Their Donut Varieties and Undeclared Peanuts in Nutty Crunch, U.S. Food & Drug Administration (FDA)
• Merrell Food Group Issues Allergy Alert on Undeclared Peanut in “Crunch’N Nutter - Mixed Nut”, U.S. Food & Drug Administration (FDA)
• Stemvida International Corporation Recalls StemAlive 90 Capsules Containing Undeclared Milk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - StemAlive 90 Capsules: Recall - Contains Undeclared Milk, FDA MedWatch
• FDA MedWatch - Rohto Eye Drops - Mentholatum: Recall - Sterility Control Review, FDA MedWatch
• Evite las estafas que parecen ser del Gobierno, GobiernoUSA.gov
• Cómo puede solicitar fondos del Gobierno para estudiar, GobiernoUSA.gov
• FDA Commissioner Margaret A. Hamburg's Statement on the 50th Anniversary Surgeon General's Report on Smoking and Health, U.S. Food & Drug Administration (FDA)
• The Mentholatum Company Issues Voluntary Nationwide Recall of Rohto® Eye Drops Made in Vietnam, U.S. Food & Drug Administration (FDA)
• Lo que necesita para declarar sus impuestos, GobiernoUSA.gov
• Enforcement Report for January 15, 2014, U.S. Food & Drug Administration (FDA)
• Mercado de Seguros Médicos y servicios preventivos, GobiernoUSA.gov
• Update of CVM's What's New - Veterinary Medication Errors, U.S. Food & Drug Administration (FDA)
• Paskesz Candy Company Issues Allergy Alert on Undeclared Milk in Premium Belgian Chocolate Coins, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Acetaminophen Prescription Combination Drug Products with more than 325 mg: FDA Statement - Recommendation to Discontinue Prescribing and Dispensing, FDA MedWatch
• FDA MedWatch - t:slim Insulin Cartridges by Tandem Diabetes Care: Recall - Potential for Cartridge Leak, FDA MedWatch
• El robo de identidad y sus impuestos, GobiernoUSA.gov
• Midwest Wholesale Issues Voluntary Recall of Boost Ultra, XZone Gold, Sexy Monkey, Triple MiracleZen Platinum, Magic for Men, "New" Extenze, and New XZen Platinum Marketed as a Dietary Supplements Due to the Presence of Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Puritan Bennett 840 Series Ventilator by Covidien - Class I Recall - Software Problem, FDA MedWatch
• FDA MedWatch - December 2013 Drug Safety Labeling Changes includes 39 products with revisions to Prescribing Information, FDA MedWatch
• FDA approves Mekinist in combination with Tafinlar for advanced melanoma, U.S. Food & Drug Administration (FDA)
• Flat Creek Farm & Dairy Recalls Cheese Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 08, 2014, U.S. Food & Drug Administration (FDA)
• The January 2014 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA approves first gel for sealing corneal incision after cataract surgery, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Covidien, Puritan Bennett 840 Series Ventilator - Software Problem, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals January 2014 Update, U.S. Food & Drug Administration (FDA)
• L.M. Noodle Company Issues Allergy Alert on Undeclared Wheat Flour, Soy Flour Whey and Milk in Butterballs, U.S. Food & Drug Administration (FDA)
• FDA approves Farxiga to treat type 2 diabetes, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sodium Phosphate Over-the-Counter Products: Drug Safety Communication - Possible Harm From Exceeding Recommended Dose, FDA MedWatch
• FDA MedWatch - Truebalance and Truetrack Blood Glucose Meters by Nipro Diagnostics: Recall - Incorrect Factory-set Measure, FDA MedWatch
• Tonia’s Biscotti II LLC Issues Allergy Alert on Undeclared Wheat, Milk, and Soy in Tonia’s Biscotti Sampler Bags, Lemon Biscotti Dipped in White Chocolate Bags, and Individually Wrapped Biscotti of All Flavors, U.S. Food & Drug Administration (FDA)
• Nipro Diagnostics, Inc. Initiates Voluntary Recall of Certain TRUEbalance and TRUEtrack Blood Glucose Meters, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - SafeSpout and SafeShower Filtration Products by Nephros: Class I Recall - Exposure to Bacteria or Virus, FDA MedWatch
• Pida gratis su informe de crédito, GobiernoUSA.gov
• Medical Device Safety and Recalls: GE Healthcare, LLC - Multi Absorber Original, Disposable - Model M1173310, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Nephros Filtration Products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - CLINIMIX and CLINIMIX E Injection/Baxter: Recall - Particulate Matter in Products, FDA MedWatch
• Baxter Initiates Nationwide Voluntary recall Of Select Lots of Premix Parenteral Nutrition, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 01, 2014, U.S. Food & Drug Administration (FDA)
• Una buena salud es clave para alcanzar sus metas, GobiernoUSA.gov
• Update of CVM's What's New - Updated Listings - Medicated Feed Mill Licenses/Veterinary Feed Directive Distributors, U.S. Food & Drug Administration (FDA)
• Deseo Rebajar Inc. Inicia un Recogido Voluntario del Producto en Cápsulas “Burn 7” Debido a Ingrediente Activo sin Declarar, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - The Ins and Outs of Extra-Label Drug Use in Animals: A Resource for Veterinarians, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - CO2 Multi Absorber by Vital Signs Devices: Field Corrective Action - Loss of Anesthetic Gases, Ventilation and Oxygenation, FDA MedWatch
• Campbell Recalls 300 Cases of Prego Traditional Italian Sauce Due to a Risk of Spoilage, U.S. Food & Drug Administration (FDA)
• The Cultured Kitchen Voluntarily Recalls Cashew Cheese Due To Possible Risk Of Contamination From Salmonella, U.S. Food & Drug Administration (FDA)
• Voluntary Field Corrective Action Initiated for Vital Signs Device’s CO2 Multi Absorber Due to a Health Risk, U.S. Food & Drug Administration (FDA)
• Consejos para una buena salud financiera, GobiernoUSA.gov
• Recursos y programas para personas de la tercera edad, GobiernoUSA.gov
• Giant Eagle Issues Allergy Alert On Undeclared Peanut Allergen In Candy Place Chocolate Santas, U.S. Food & Drug Administration (FDA)
• Zip International Group LLC Recalls FOSFOREL Herring Fillet in Oil Due to Potential Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Baxter 5 Percent Dextrose Injection, USP And 0.9 Percent Sodium Chloride Injection, USP Intravenous (IV) Solutions: Recall - Particulate Matter In Solution, FDA MedWatch
• Baxter Initiates Worldwide Voluntary Recall Of Select Lots Of 5 percent Dextrose Injection, USP And 0.9 percent Sodium Chloride Injection, USP Intravenous (IV) Solutions, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 26, 2013, U.S. Food & Drug Administration (FDA)
• Deseo Rebajar Inc. Issues Voluntary Recall of Burn 7 Capsules Due to Undeclared Active Ingredient, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lidocaine HCl Injection 2%, 5 ml Vial by Hospira: Recall - Presence of Particulate Matter, FDA MedWatch
• Hospira Issues a Voluntary Nationwide Recall of One Lot of Lidocaine HCl Injection, USP, 2%, 5 Ml in 5 Ml Vial, Due to Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Muscle Growth Product Called Mass Destruction: FDA Health Risk Warning - Undeclared Ingredients, FDA MedWatch
• FDA warns consumers not to use muscle growth product, U.S. Food & Drug Administration (FDA)
• FDA approves Tretten to treat rare genetic clotting disorder, U.S. Food & Drug Administration (FDA)
• Spokane Produce, Inc. Voluntarily Recalls Victor™ Toasted Sesame Hummus Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Concertos in Chocolate Issues Allergy Alert on Milk in Solid Milk Chocolate Santa, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - New Isentress (raltegravir) dosage form: oral suspension, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Changes to the Baraclude (entecavir) package and label, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - New PegIntron Selectdose, U.S. Food & Drug Administration (FDA)
• Make 2014 Your Healthiest Year Yet, FDA Office of Women's Health
• Conozca por dónde anda Papá Noel durante la Nochebuena, GobiernoUSA.gov
• FDA MedWatch - Abrams Royal Pharmacy Sterile Products - Recall - Lack of Sterility Assurance, FDA MedWatch
• Abrams Royal Pharmacy Issues Voluntary Nationwide Recall of All Lots of Unexpired Sterile Products Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 18, 2013, U.S. Food & Drug Administration (FDA)
• FDA approves Anoro Ellipta to treat chronic obstructive pulmonary disease, U.S. Food & Drug Administration (FDA)
• FDA and European Medicines Agency launch generic drug application inspections initiative, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Methylphenidate ADHD Medications: Drug Safety Communication - Risk of Long-lasting Erections, FDA MedWatch
• Megabusiness LLC Issues Alert on Undeclared Sulfites in Del Campo Papa Seca / DRY Potato 24x14 oz., U.S. Food & Drug Administration (FDA)
• Bee International Expands Allergy Alert on Undeclared Egg in "Sweet Spots", U.S. Food & Drug Administration (FDA)
• Prevenga la gripe en esta temporada, GobiernoUSA.gov
• Lock up your medicines to protect children and teens this holiday season, U.S. Food & Drug Administration (FDA)
• Cómo preparar comidas saludables para las fiestas, GobiernoUSA.gov
• Blooming Import Inc. Issues an Alert on Undeclared Sulfites in Farmer Brand Dried Lily Flowers, U.S. Food & Drug Administration (FDA)
• Stone Independent Research, Inc. Issues Allergy Alert on Undeclared Milk in One Lot of Zanocap Capsules, U.S. Food & Drug Administration (FDA)
• Stone Independent Research, Inc. Issues Allergy Alert on Undeclared Milk in EnhanceRx Dietary Supplement, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Food Safety Modernization Act and Animal Feed, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Food Safety Modernization Act and Animal Feed, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Food Safety Modernization Act and Animal Feed, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Soliris (Eculizumab) Concentrated Solution for Intravenous Infusion by Alexion: Recall - Visible Particles, FDA MedWatch
• Medical Device Safety and Recalls: FDA Announces Improvements To The Medical Device Recalls Database, U.S. Food & Drug Administration (FDA)
• Alexion Provides Update on Previously Communicated November 2013 Voluntary Nationwide Recall of Two Lots of Soliris (eculizumab) Concentrated Solution for Intravenous Infusion, U.S. Food & Drug Administration (FDA)
• Bee International Issues Allergy Alert on Undeclared Egg in "Sweet Spots", U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update – changes to Complera (emtricitabine, rilpivirine, tenofovir disoproxil fumarate) labeling for HIV/AIDS, U.S. Food & Drug Administration (FDA)
• Publicaciones en español gratis para un año más saludable, GobiernoUSA.gov
• Pin Hsiao & Associates, LLC. Issues Allergy Alert on Undeclared Walnuts in Gluten Free Blueberry Mini Muffins - 12 pk., U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 11, 2013, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nipple Aspirate Test: Safety Communication - Breast Cancer Screening Test Is Not An Alternative To Mammography, FDA MedWatch
• Blooming Import Inc. Issues an Alert on Undeclared Sulfites in Golden Lion Brand Dried Ziziphus Jujuba Mill (Dried Dates), U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Breast Cancer Screening - Nipple Aspirate Test Is Not An Alternative To Mammography, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Mid-Atlantic Region Recalls Spinach Dip Due to Undeclared Egg, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Answers Your Questions about Fish Drugs, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Judicious Use of Antimicrobials, U.S. Food & Drug Administration (FDA)
• Health Matters America Inc. Issues an Allergy Alert on Undeclared Milk in Organic Traditions Brand Dark Chocolate Hazelnuts, Dark Chocolate Hazelnuts with Chili, Dark Chocolate Almonds, and Dark Chocolate Almonds with Chili., U.S. Food & Drug Administration (FDA)
• FDA approves first generic versions of antidepressant drug Cymbalta, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Takes Significant Steps to Address Antimicrobial Resistance, U.S. Food & Drug Administration (FDA)
• FDA takes significant steps to address antimicrobial resistance, U.S. Food & Drug Administration (FDA)
• Cómo hacer envíos para Navidad por correo postal, GobiernoUSA.gov
• The December 2013 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Approval of Sovaldi (sofosbuvir) tablets for the treatment of chronic hepatitis C, U.S. Food & Drug Administration (FDA)
• El agua potable y su salud, GobiernoUSA.gov
• FDA approves first drug treatment for Peyronie’s disease, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - November 2013 Drug Safety Labeling Changes includes 27 products with revisions to Prescribing Information, FDA MedWatch
• Enforcement Report for December 04, 2013, U.S. Food & Drug Administration (FDA)
• Todos tienen que tener un seguro de salud en el 2014, GobiernoUSA.gov
• Infórmese sobre leyes que prohíben discriminación por discapacidad, GobiernoUSA.gov
• Update of CVM's What's New - Animal Drug Approvals December 2013 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Philips HeartStart FRx, HeartStart HS1 Home, and HeartStart HS1 OnSite Automated External Defibrillators (AED), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Cargill Conducts Voluntary Recall of Select Nutrena® NatureWise® Meatbird and Chick Starter Feed, U.S. Food & Drug Administration (FDA)
• Cargill Conducts Voluntary Recall of Select Nutrena® NatureWise® Meatbird and Chick Starter Feed, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HeartStart Automated External Defibrillators (AED) From Philips Healthcare: Safety Communication - Failure Of An Electrical Component That Could Cause AEDs To Fail To Deliver Appropriate Shock, FDA MedWatch
• FDA issues safety communication on HeartStart automated external defibrillators from Philips Healthcare, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Addresses Continued Shortage of Drug Used to Treat Heartworm Infection in Dogs, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Onfi (clobazam): Drug Safety Communication - Risk of Serious Skin Reactions, FDA MedWatch
• Huxtable’s Kitchen Issues Voluntary Allergy Alert on Undeclared Allergens in Butternut Squash & Creamed Spinach Gratin, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Resolved Drug Shortage for Xylazine, U.S. Food & Drug Administration (FDA)
• Recomendaciones para comprar juguetes seguros, GobiernoUSA.gov
• IQ Formulations Issues a Voluntary Recall of HYDRAVAX Dietary Supplement Due to Possible Undeclared Ingredient, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - FreeStyle and FreeStyle Lite Blood Glucose Test Strips by Abbott: Recall - Erroneously Low Blood Glucose Results, FDA MedWatch
• Abbott Issues Voluntary Recall of Certain FreeStyle® and FreeStyle Lite® Blood Glucose Test Strips in the United States, U.S. Food & Drug Administration (FDA)
• Flat Creek Farm and Dairy Recalls Heavenly Blue Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 27, 2013, U.S. Food & Drug Administration (FDA)
• No maneje tomado, GobiernoUSA.gov