FDA News Releases

• Date Index

• FDA MedWatch - Baxter IV Solutions (Select Lots): Recall - Potential for Leaking Containers and Particulate Matter, FDA MedWatch
• Baxter initiates Voluntary Nationwide Recall of Select Lots of IV Solutions Due to the Potential for Leaking Containers and Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Optisure Dual Coil Defibrillation Leads by St. Jude Medical: Class I Recall - Damage May Prevent Patient Therapy, FDA MedWatch
• AA USA Trading Inc. Issues Allergy Alert on Undeclared Sulfites and Colors in AA Brand Dried Kiwi and Dried Mango, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 20, 2016, U.S. Food & Drug Administration (FDA)
• Dole Fresh Vegetables Announces Voluntary Withdrawal for Salads, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Carnivore Meat Company, LLC Voluntarily Issues a Recall for One Lot of Frozen Pet Food, U.S. Food & Drug Administration (FDA)
• Carnivore Meat Company, LLC Voluntarily Issues a Recall for One Lot of Frozen Pet Food, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Import Tolerances for monepantel available, U.S. Food & Drug Administration (FDA)
• Mahina Mele Farms, LLC Recalls Macadamia Nut Products Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Read about Research Roadmap, Clinical Trials and more in the January FDA Women's Health eUpdate, FDA Office of Women's Health
• Master Herbs, Inc. Issues Voluntary Nationwide Recall of All Lots of Licorice Coughing Liquid Due to the Presence of Morphine, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Biannual Progress Report on Judicious Use of Antimicrobials in Food-producing Animals, U.S. Food & Drug Administration (FDA)
• Alerta para viajeros: protéjase del virus del Zika, GobiernoUSA.gov
• CVM Updates - FDA Issues Final Guidance for Target Animal Safety Data Presentation, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Case Examples of Veterinary Medication Errors, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Guidelines App available for iOS and Android Devices, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Guidances Under Development for 2016 Available, U.S. Food & Drug Administration (FDA)
• Fresh Express Announces Precautionary Recall of a Limited Quantity of 12 oz. Baby Spinach Due to Possible Allergen Exposure, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Abbott's Compounding Pharmacy Issues Voluntary Recall of All Lots of Unexpired Sterile Human and Animal Compounded Products Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Blendtech Issues Allergy Alert on Undeclared Milk Allergen in Uncle Buck's Fish Batter Mix - Original, U.S. Food & Drug Administration (FDA)
• Perrigo Initiates Voluntary Product Recall in the U.S. Of Children's Guaifenesin Grape Liquid and Guaifenesin DM Cherry Liquid Due to a Potential Defect with the Dosage Cup, U.S. Food & Drug Administration (FDA)
• Abbott's Compounding Pharmacy Issues Voluntary Recall of All Lots of Unexpired Sterile Human and Animal Compounded Products Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Heritage International (USA) Inc, Voluntarily Recalls One Lot of Raw Cashew Pieces Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Unexpired Sterile Human and Animal Compounded Products by Abbott's Compounding Pharmacy: Recall - Lack of Sterility Assurance, FDA MedWatch
• FDA MedWatch - Licorice Coughing Liquid OTC Cough Syrup by Ma Ying Long Pharmaceutical Group: CDER Alert - Contains Unidentified Morphine, FDA MedWatch
• Medical Device Safety and Recalls: Brainlab Cranial Image-Guided Surgery (IGS) System – Navigation Inaccuracy, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Brainlab Cranial Image-Guided Surgery (IGS) System: Class I Recall - Navigation Inaccuracy, FDA MedWatch
• FDA MedWatch - Duodenoscope Model TJF-Q180V by Olympus: UPDATED FDA Safety Communication, New Reprocessing Instructions Validated, FDA MedWatch
• Cinco pasos para estar listo para las elecciones primarias, GobiernoUSA.gov
• Make a Difference in Women’s Health: Support Diverse Women in Clinical Trials, FDA Office of Women's Health
• Cuidemos los dientes, son para toda la vida, GobiernoUSA.gov
• FDA MedWatch - December 2015 Drug Safety Labeling Changes includes 31 products with revisions to Prescribing Information, FDA MedWatch
• FDA MedWatch - Children's Guaifenesin Grape Liquid and Guaifenesin DM Cherry Liquid by Perrigo Company: Recall - Potential Defect with Dosage Cup, FDA MedWatch
• ¿Tiene preguntas sobre la votación presidencial y las primarias?, GobiernoUSA.gov
• Medical Device Safety and Recalls: Stryker Fuhrman Pleural and Pneumopericardial Drainage Sets, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Pleural and Pneumopericardial Drainage Sets by Stryker Fuhrman - Class I Recall - Catheter May Break During Insertion, FDA MedWatch
• Kermit, Inc. Issues Allergy Alert on Undeclared Soy and Anchovies in Various Barbecue Sauces, U.S. Food & Drug Administration (FDA)
• Federal judge enters consent decree against Downing Labs, U.S. Food & Drug Administration (FDA)
• The Easiest Thing You Can Do to Prevent Foodborne Illness, FoodSafety.gov
• The January 2016 MedSun Newsletter is now available, U.S. Food & Drug Administration (FDA)
• Good Earth Egg Company Voluntarily Recalls Shell Eggs Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Importante: se acerca la fecha límite de la Inscripción Abierta, GobiernoUSA.gov
• FDA MedWatch - Multiple Products by R Thomas Marketing: Recall - Undeclared Drug Ingredient, FDA MedWatch
• FDA MedWatch - L.G Compounded Asafoetida Powder by Shakti Group: Recall - Potential Contamination with Salmonella, FDA MedWatch
• Shakti Group USA LLC Recalls L.G Compounded Asafoetida Powder Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 30, 2015, U.S. Food & Drug Administration (FDA)
• Giant Eagle Cleveland Voluntarily Recalls New Year's Pretzels from Select Stores Due to an Undeclared Walnut Allergen, U.S. Food & Drug Administration (FDA)
• Giant Eagle Pittsburgh Voluntarily Recalls New Year's Pretzels from Select Stores Due to an Undeclared Walnut Allergen, U.S. Food & Drug Administration (FDA)
• Market District Voluntarily Recalls New Year's Pretzels Due to an Undeclared Walnut Allergen, U.S. Food & Drug Administration (FDA)
• Giant Eagle Youngstown Voluntarily Recalls New Year's Pretzels from Select Stores Due to an Undeclared Walnut Allergen, U.S. Food & Drug Administration (FDA)
• Milky Way International Trading Corp. Issues Voluntary Nationwide Recall of Nice! Mandarin Oranges in 8-ounce Bottles Due to Possible Glass in Products, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals January 2016 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Cape Cod Provisions LLC Issues Allergy Alert on Undeclared Almonds in Product, U.S. Food & Drug Administration (FDA)
• US Marshals seize dietary supplements containing kratom, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Dräger Evita V500 and Babylog VN500 Ventilators - Issue with Optional PS500 Battery Power Supply May Cause Ventilators to Shut Down Unexpectedly, U.S. Food & Drug Administration (FDA)
• Hospira Issues a Voluntary Nationwide Recall of One Lot of Magnesium Sulfate in Water for Injection Due to Incorrect Barcode Labeling on the Primary Container, U.S. Food & Drug Administration (FDA)
• The FDA engages stakeholders on opportunities to improve hearing aid usage and innovation, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Evita V500 and Babylog VN500 Ventilators by Dräger: Class I Recall - Issue with Optional PS500 Battery Power Supply May Cause Ventilators to Shut Down Unexpectedly, FDA MedWatch
• FDA MedWatch - Magnesium Sulfate in Water for Injection by Hospira: Recall - Incorrect Barcode Labeling on the Primary Container, FDA MedWatch
• Medical Device Safety and Recalls: The FDA Recommends Health Care Providers Stop Using Customed, Inc. Surgical Convenience Packs and Trays: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Baxter IV Solutions: Recall - Potential Presence of Particulate Matter, FDA MedWatch
• 4 Easy Resolutions to Keep Food Safe, FoodSafety.gov
• Baxter Initiates Voluntary Recall of Two Lots of IV Solutions due to Potential Presence of Particulate Matter, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Big Dog Natural Recalls Chicken and Fish Supreme Dog Food Due to Possible Salmonella and Listeria monocytogenes Health Risk, U.S. Food & Drug Administration (FDA)
• Big Dog Natural Recalls Chicken and Fish Supreme Dog Food Due to Possible Salmonella and Listeria monocytogenes Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Noxafil (posaconazole): Drug Safety Communication - Dosing Errors when Switching between Different Oral Formulations; Label Changes Approved, FDA MedWatch
• FDA strengthens requirements for surgical mesh for the transvaginal repair of POP, FDA Office of Women's Health
• FDA strengthens requirements for surgical mesh for the transvaginal repair of pelvic organ prolapse to address safety risks, U.S. Food & Drug Administration (FDA)
• Pharmedium Issues Voluntary Nationwide Recall of 4mg Norepinephrine Bitartrate (16mcg/mL) Added to 0.9% Sodium Chloride in 250mL Viaflex Bag and 8mg Norepinephrine Bitartrate (32mcg/mL) Added to 0.9% Sodium Chloride in 250mL Viaflex Bag for Discoloration., U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 4mg Norepinephrine Bitartrate (16mcg/mL) Added to 0.9% Sodium Chloride in 250mL Viaflex Bag and 8mg Norepinephrine Bitartrate (32mcg/mL) Added to 0.9% Sodium Chloride in 250mL Viaflex Bag by Pharmedium: Recall - Discoloration, FDA MedWatch
• Thomas Produce Recalls Cucumbers because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: bioMérieux SA Etest® PIP/TAZO/CON-4 PTC 256 – Potential for Test Result Error, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Etest PIP/TAZO/CON-4 PTC 256 by bioMérieux: Class I Recall – Potential for Test Result Error, FDA MedWatch
• Food Safety Highlights from 2015, FoodSafety.gov
• Uoriki Fresh, Inc. Recalls "Octopus Salad" Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• ¡Felices fiestas!, GobiernoUSA.gov
• Taylor Farms Pacific, Inc. Recalls Signature Cafe Traditional Stuffing Due to Potential Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Nuway Distributors llc Issues Voluntary [Worldwide/Nationwide] Recall of APEXXX Due to Presence of Undeclared Sildenafil, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Updated Comment Period for "Natural" in Food Labeling, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: FUJIFILM Medical Systems, U.S.A., Inc. Validates Revised Reprocessing Instructions for Model ED-530XT Duodenoscopes: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 23, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Apexxx by Nuway Distributors: Recall - Undeclared Drug Ingredient, FDA MedWatch
• FDA MedWatch - ED-530XT Duodenoscopes by FUJIFILM Medical Systems, U.S.A.: Safety Communication - FUJIFILM Medical Systems Validates Revised Reprocessing Instructions, FDA MedWatch
• FDA MedWatch - Perseus A500 Anesthesia Workstation by Draeger: Class I Recall - Faulty Power Switch May Cause Device to Stop Working, FDA MedWatch
• Medical Device Safety and Recalls: Notification of Three Recalls, U.S. Food & Drug Administration (FDA)
• American Pure Whey Issues Allergy Alert on Undeclared Milk and Soy in Whey Protein Products., U.S. Food & Drug Administration (FDA)
• Urgent: Drug Recall - Weight Loss Dietary Supplements with Undeclared Sibutramine and Phenolphthalein, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - La' Trim Plus, Jenesis and Oasis by BeeXtreme: Recall - Undeclared Drug Ingredients, FDA MedWatch
• FDA MedWatch - Various Products Distributed for Weight Loss by Bee Extremely Amazed: Recall - Undeclared Drug Ingredients, FDA MedWatch
• Bee Extremely Amazed LLC Issues Voluntary Nationwide Recall of Various Products Distributed For Weight Loss Due to Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• Ocean Group, Inc. Announces Recall of Ocean Brand Masago Lake Smelt Roe for Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• FDA Press Releases Update, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hand-held Laser Pointers: FDA Safety Communication - Risk of Eye and Skin Injuries, FDA MedWatch
• Laser Pointer Safety Communication and Video, U.S. Food & Drug Administration (FDA)
• What NOT to Eat This Holiday, FoodSafety.gov
• FDA approves new orphan drug to treat pulmonary arterial hypertension, U.S. Food & Drug Administration (FDA)
• The Swinomish Fish Company Voluntarily Recalls Native Catch Salmon Bacon Because of a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA updates blood donor deferral policy to reflect the most current scientific evidence and continue to ensure the safety of the U.S. blood supply, U.S. Food & Drug Administration (FDA)
• Indoor Tanning Bed Restrictions and more in the December FDA Women's Health Update, FDA Office of Women's Health
• CFSAN Constituent Update - FDA Creates the Office of Dietary Supplement Programs and Announces New Nutrition Office Leadership, U.S. Food & Drug Administration (FDA)
• Final guidance, “Revised Recommendations for Reducing the Risk of Human Immunodeficiency Virus Transmission by Blood and Blood Products.”, U.S. Food & Drug Administration (FDA)
• Mars Chocolate North America Issues Allergy Alert Voluntary Recall on Undeclared Peanuts, Wheat and Egg Ingredient for DOVE® Chocolate Assortment Snowflakes, 24.0 oz. Bag, Sold Only at One Major Retailer with Stores Across the U.S., U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Smart Lipo: Recall - Undeclared Drug Ingredients, FDA MedWatch
• Voluntary Recall Notice for Zatarain's Red Beans and Rice Original due to Possible Health Risk from Undeclared Ingredients, U.S. Food & Drug Administration (FDA)
• SmartLipo365 Issues Voluntary Nationwide Recall of Smart Lipo Due to Undeclared Sibutramine, Desmethylsibutramine and Phenolphthalein, U.S. Food & Drug Administration (FDA)
• Invirase Labeling Updated, U.S. Food & Drug Administration (FDA)
• Holiday Tips for Junior Chefs: Keep Kids Safe in the Kitchen, FoodSafety.gov
• FDA proposes tanning bed age restrictions and other important safety measures, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 16, 2015, U.S. Food & Drug Administration (FDA)
• FDA approves wearable defibrillator for children at risk for sudden cardiac arrest, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Keep Your Dogs and Cats Safe From Holiday Hazards, U.S. Food & Drug Administration (FDA)
• CVM Updates - Updated - FDA Announces Pending Withdrawal of Approval of Nitarsone, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Rosiglitazone-containing Diabetes Medicines: Drug Safety Communication - FDA Eliminates the Risk Evaluation and Mitigation Strategy (REMS), FDA MedWatch
• Trader Joe's Issues Voluntary Recall of Triple Ginger Brew, U.S. Food & Drug Administration (FDA)
• Stella & Chewy's Voluntarily Recalls Frozen Dinner Morsel Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Publicaciones en español gratis: cuide su dinero y asegure su futuro, GobiernoUSA.gov
• FDA approves Bridion to reverse effects of neuromuscular blocking drugs used during surgery, U.S. Food & Drug Administration (FDA)
• Sun Noodle- New Jersey- Issues Allergy Alert on Undeclared Egg in Tonkotsu Ramen, U.S. Food & Drug Administration (FDA)
• FDA takes action against Vermont dairy farm for illegally administering drugs to cattle, U.S. Food & Drug Administration (FDA)
• A Latino's Food Safety Guide to “Navidad” & “Fin de Año”, FoodSafety.gov
• Enforcement Report for December 09, 2015, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Bravo Recalls Select Chicken and Turkey Pet Foods Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Reesna Inc., Issues a Voluntary Nationwide Recall of Fuel Up Plus and Fuel Up High Octane due to the Presence of Undeclared Hydroxythiohomosildenafil, U.S. Food & Drug Administration (FDA)
• FDA approves new oral therapy to treat ALK-positive lung cancer, U.S. Food & Drug Administration (FDA)
• FDA approves first emergency treatment for overdose of certain types of chemotherapy, U.S. Food & Drug Administration (FDA)
• Bravo Recalls Select Chicken and Turkey Pet Foods Because of Possible Salmonella Health Risk., U.S. Food & Drug Administration (FDA)
• Pine Valley Foods, Inc. Voluntarily Recalls Crazy About Cookie Products Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Voluntary Recall Of Chariot Guiding Sheath, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - November 2015 Drug Safety Labeling Changes includes 19 products with revisions to Prescribing Information, FDA MedWatch
• FDA MedWatch - Chariot Guiding Sheath by Boston Scientific: Recall - Risk of Shaft Separation, FDA MedWatch
• What Not to Bring to Your Next Holiday Party, FoodSafety.gov
• The Sweet Leaf Tea Company Issues Voluntary Nationwide Recall of Tea in Glass Bottles, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Annual Summary Report on Antimicrobials Sold or Distributed in 2014 for Use in Food-Producing Animals, U.S. Food & Drug Administration (FDA)
• The Morrison Milling Company Voluntary and Precautionary Recall of Corn Products, U.S. Food & Drug Administration (FDA)
• Lucy's Weight Loss System Issues Voluntary Nationwide Recall of Pink Bikini Dietary Supplement Due to Undeclared Diclofenac, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Baclofen Active Pharmaceutical Ingredient from Taizhou Xinyou Pharmaceutical and Chemical: FDA Statement - FDA Warns of Potential Contamination, FDA MedWatch
• FDA MedWatch - Pink Bikini Dietary Supplement by Lucy's Weight Loss System: Recall - Undeclared Drug Ingredient, FDA MedWatch
• Medical Device Safety and Recalls: eVent Medical LS, 5i, or 7i Inspiration Ventilators May Shut Down without Alarm, U.S. Food & Drug Administration (FDA)
• FDA approves first recombinant von Willebrand factor to treat bleeding episodes, U.S. Food & Drug Administration (FDA)
• FDA approves first drug to treat a rare enzyme disorder in pediatric and adult patients, U.S. Food & Drug Administration (FDA)
• Kroger Recalls Bakery Fresh Goodness Chocolate Brownies Due to Undeclared Allergens, U.S. Food & Drug Administration (FDA)
• Delicious Doorstep Deliveries: How to Keep Them Safe, FoodSafety.gov
• The December 2015 MedSun Newsletter is now available, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Inspiration LS, 5i and 7i Ventilator Systems by eVent Medical: Class I Recall - May Shut Down without Alarm, FDA MedWatch
• Aprenda a manejar el estrés y la ansiedad que aparecen después de una catástrofe, GobiernoUSA.gov
• Enforcement Report for December 02, 2015, U.S. Food & Drug Administration (FDA)
• Lipo Escultura Corp. Issues Nationwide Recall of Lipo Escultura Due to Undeclared Sibutramine and Diclofenac, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - SGLT2 Inhibitors: Drug Safety Communication - Labels to Include Warnings About Too Much Acid in the Blood and Serious Urinary Tract Infections, FDA MedWatch
• FDA MedWatch - Lipo Escultura: Recall - Undeclared Drug Ingredients, FDA MedWatch
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update: Warning & Untitled Letters to Industry Citing Color Additive, U.S. Food & Drug Administration (FDA)
• Inscríbase HOY en el Mercado de Seguros Médicos, GobiernoUSA.gov
• CVM Updates - FDA Announces Minor Use/Minor Species (MUMS) Grant Program Request for Applications Due January 15, 2016, U.S. Food & Drug Administration (FDA)
• JEM Raw Chocolate LLC Voluntarily Recalls Nut Butter Spread Products Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Insulet Corporation Issues Field Safety Notification of OmniPod Insulin Management System, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - OmniPod Insulin Management System by Insulet: Field Safety Notification - Reported Cases of Needle Mechanism Deployment Failure or Delay, FDA MedWatch
• Update of CVM's What's New - Animal Drug Approvals December 2015 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Three Holiday Gift Ideas for Home Chefs, FoodSafety.gov
• Enforcement Report for November 25, 2015, U.S. Food & Drug Administration (FDA)
• La Inscripción Abierta de Medicare termina el 7 de diciembre, GobiernoUSA.gov
• FDA MedWatch - Digital Temple Thermometer (DTT) by K-Jump Health Co., Ltd.: Recall - Inaccurate Temperature Display, FDA MedWatch
• Bestmed, LLC Issues Nationwide Recall Of Digital Temple Thermometer (DTT?), Model No. KD-2201 Manufactured By K-Jump Health Co., Ltd., U.S. Food & Drug Administration (FDA)
• Nuevo examen de práctica para aspirantes a la ciudadanía de EE. UU., GobiernoUSA.gov
• FDA Basics Webinar- Dec 1: Role of FDA in HIV Diagnosis, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Boston Scientific’s RotaWire Elite Guidewire and wireClip Torquer Guidewire May Break and Separate from the Rotablator System, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Draft Guidance on Veterinary Feed Directive Common Format, U.S. Food & Drug Administration (FDA)
• Noviembre es el Mes de la Herencia Nativa Americana, GobiernoUSA.gov
• Update of CVM's What's New - Blue Buffalo Voluntarily Recalls One Lot of Cub Size Wilderness Wild Chews Bones Due to Potential Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Announces Glades Drugs' Nationwide Voluntary Recall Of Compounded Multivitamins Containing High Amounts Of Vitamin D3 (Cholecalciferol), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - RotaWire Elite Guidewire and wireClip Torquer Guidewire by Boston Scientific: Recall - Wires May Break and Separate from the Rotablator System, FDA MedWatch
• Taylor Farms Pacific, Inc. Recalls Celery Products Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Fuel Up for Black Friday with Leftovers from Thanksgiving, FoodSafety.gov
• FDA MedWatch - Compounded Multivitamins by Glades Drugs: Voluntary Recall - High Amounts of Vitamin D3 (Cholecalciferol), FDA MedWatch
• Bertagni 1882 Spa Issues Allergy Alert On Undeclared Almond And Cashew In Butternut Squash Ravioli, U.S. Food & Drug Administration (FDA)
• Blue Buffalo Voluntarily Recalls One Lot of Cub Size Wilderness Wild Chews Bones Due to Potential Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Raley's Family of Fine Stores Issues Allergy Alert on Undeclared Cashew and Almond in Raley's Frozen Sweet Pumpkin Ravioli, U.S. Food & Drug Administration (FDA)
• Read about Essure, Diabetes and more in the November FDA Women's Health eUpdate, FDA Office of Women's Health
• 3 Steps to Confidently Cooking Turkey, FoodSafety.gov
• HOY! Expertos contestarán sus preguntas en vivo, GobiernoUSA.gov
• Mi Tienda Issues Precautionary Recall: Recall Affects Masa and Tostadas Purchased ONLY at Mi Tienda #1 Located at 1630 Spencer Highway, South Houston, TX, U.S. Food & Drug Administration (FDA)
• FDA approves Opdivo to treat advanced form of kidney cancer, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - New Resource on Sampling, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Lubricious Coating Separation from Intravascular Medical Devices: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Food From Genetically Engineered Plants Is Safe To Eat, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Intravascular Medical Devices: FDA Safety Communication - Lubricious Coating Separation, FDA MedWatch
• Casey's Bakery Inc. Issues Allergy Alert On Undeclared Peanuts in Snickers 8x8 Cake, U.S. Food & Drug Administration (FDA)
• Expertos contestarán sus preguntas en vivo el próximo martes, GobiernoUSA.gov
• One Week Left - Are You Ready for Thanksgiving?, FoodSafety.gov
• Fit Firm and Fabulous Issues Voluntary Nationwide Recall of Ultimate Herbal Slimcaps Due to the Presence of Undeclared Sibutramine, U.S. Food & Drug Administration (FDA)
• FDA takes several actions involving genetically engineered plants and animals for food, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA takes several actions involving genetically engineered plants and animals for food, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 18, 2015, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - CHS Inc. Issues Voluntary Recall of Certain Kountry Buffet and Provider Pellet Products Due to Excessive Copper, U.S. Food & Drug Administration (FDA)
• Wegmans Food Markets Issues Allergy Alert on Undeclared Tree Nuts (Cashews and Almonds) in Wegmans Italian Classics Butternut Squash Ravioli, 9 oz., U.S. Food & Drug Administration (FDA)
• CHS Inc. Issues Voluntary Recall of Certain Kountry Buffet and Provider Pellet Products Due to Excessive Copper, U.S. Food & Drug Administration (FDA)
• Ashdon Farms Issues Allergy Alert on Honey Mustard Pretzel Mix and Honey Mustard Mix, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Blackhead Disease Mini-Symposium at the 2016 AVMA convention in San Antonio, TX – Request for Abstracts, U.S. Food & Drug Administration (FDA)
• Answers to Your Top Turkey Questions, FoodSafety.gov
• FDA MedWatch - Iodine-containing Contrast Agents for Medical Imaging: Drug Safety Communication - Rare Cases of Underactive Thyroid in Infants, FDA MedWatch
• CFSAN Constituent Update - Gluten-Free Labeling Compliance Requirements, U.S. Food & Drug Administration (FDA)
• FDA Orders Recall under Consent Decree for all Custom Ultrasonics Automated Endoscope Reprocessors, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 11, 2015, U.S. Food & Drug Administration (FDA)
• Actualización - Diabetes: ¿Busca información confiable y actualizada?, GobiernoUSA.gov
• Diabetes: ¿Buscas información confiable y actualizada?, GobiernoUSA.gov
• SpaghettiOs Original 14.2oz Cans Recalled Due to Potential Choking Hazard, U.S. Food & Drug Administration (FDA)
• Homestat Farm Recalls Organic Steel Cut Oats & Chia With Flax And Rye Flakes Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Virginia Diner, Inc. Issues Allergy Alert on Undeclared Peanut Allergen in Pecan Turtledoves Chocolate Caramel Pecan Clusters (Candy), U.S. Food & Drug Administration (FDA)
• Giant Eagle Voluntarily Recalls Apricot Logs and Poppyseed Logs Due to an Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• HARVONI (ledipasvir/sofosbuvir) label updated, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Endoscope Washer/Disinfectors by Custom Ultrasonics: Safety Communication - FDA Recommends Health Care Facilities Transition to Alternate Reprocessing Methods, FDA MedWatch
• Vivir con diabetes: ¡digamos sí a la buena salud!, GobiernoUSA.gov
• Medical Device Safety and Recalls: FDA Recommends Health Care Facilities Transition from Custom Ultrasonics Endoscope Washer/Disinfectors to Alternate Reprocessing Methods: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Hamilton Recalls G5 Ventilator Because of Ventilation and Alarm Failure, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - October 2015 Drug Safety Labeling Changes includes 26 products with revisions to Prescribing Information, FDA MedWatch
• FDA MedWatch - G5 Ventilator by Hamilton: Class I Recall - Ventilation and Alarm Failure, FDA MedWatch
• 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)
• CFSAN Constituent Update - Groundbreaking Rules on Produce and Imported Foods, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Final Environmental Impact Statement on Produce Rule, U.S. Food & Drug Administration (FDA)
• Trader Joe’s Issues Voluntary Allergy Alert on Tree Nuts In Trader Giotto’s Butternut Squash Triangoli, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Halo, Purely for Pets® Issues Voluntary Recall of Sensitive Cat Turkey Dry Food Due to Mold, U.S. Food & Drug Administration (FDA)
• Halo, Purely for Pets® Issues Voluntary Recall of Sensitive Cat Turkey Dry Food Due to Mold, U.S. Food & Drug Administration (FDA)
• Old Oregon Smokehouse is Issuing a Voluntary Recall Canned Albacore Tuna Because of a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Día de los Veteranos: conozca más sobre beneficios para militares, GobiernoUSA.gov
• 5 Things You Can Do Today to Prepare for a Safe Thanksgiving, FoodSafety.gov
• FDA Webinar: November 12, 2015: Generic Drugs and FDA's Orange Book, U.S. Food & Drug Administration (FDA)
• Brett Anthony Foods Issues Allergy Alert on Undeclared Chestnuts in Whole Foods Brand Wild Mushroom Soup Sold in Illinois, Indiana, Michigan, Missouri, Minnesota and Nebraska Stores, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CFSAN Constituent Update, U.S. Food & Drug Administration (FDA)
  • CFSAN Constituent Update, U.S. Food & Drug Administration (FDA)
  • CFSAN Constituent Update, U.S. Food & Drug Administration (FDA)
  • CFSAN Constituent Update, U.S. Food & Drug Administration (FDA)
  • CFSAN Constituent Update, U.S. Food & Drug Administration (FDA)
• Inaffit, LLC Issues Voluntary Nationwide Recall of Natureal Due to Undeclared Sibutramine, U.S. Food & Drug Administration (FDA)
• Diabetes: no se quede con dudas, GobiernoUSA.gov
• Zenobia Company LLC. Recalls Ground Flax Seed Meal Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• The November 2015 MedSun Newsletter is now available, U.S. Food & Drug Administration (FDA)
• Blue Buffalo Company, Ltd. Voluntarily Recalls Limited Production of Kitty Yums Chicken Recipe Cat Treats Due to the Presence of Propylene Glycol, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Blue Buffalo Company, Ltd. Voluntarily Recalls Limited Production of Kitty Yums Chicken Recipe Cat Treats Due to the Presence of Propylene Glycol, U.S. Food & Drug Administration (FDA)
• World Variety Produce, Inc. Voluntarily Recalls Italian Pine Nuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Brett Anthony Foods Issues Allergy Alert on Undeclared Peanut, Egg, Sulfite in Whole Foods Brand Tofu Curry Cous Cous Box 16oz, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 04, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Plavix (clopidogrel): Drug Safety Communication - Long-term Treatment Does Not Change Risk of Death, FDA MedWatch
• Kozy Shack Recalls One Lot of Kozy Shack Indulgent Recipe Pudding, U.S. Food & Drug Administration (FDA)
• Peru Food Imports, Inc. Issues Allergy Alert on Undeclared Sulfites in Mote Corn-Maiz Mote, Lot# 38-16, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Issues Guidance on Fortification of Foods, U.S. Food & Drug Administration (FDA)
• ¿Tiene preguntas sobre la votación y las elecciones?, GobiernoUSA.gov
• What do the Government & Food Industry Have in Common?, FoodSafety.gov
• FDA approved GENVOYA as a complete regimen for the treatment of HIV-1 infection, U.S. Food & Drug Administration (FDA)
• FDA approves new treatment for HIV, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals November 2015 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Tate's Bake Shop Issues Allergy Alert on Undeclared Walnut Allergen in Tate's 7oz Chocolate Chip Cookies And Tate's 7oz Ginger Zinger Cookies., U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Final Guidance: HIV-1 Infection: Developing Antiretroviral Drugs for Treatment, U.S. Food & Drug Administration (FDA)
• ¿Ya solicitó su cobertura médica para 2016?, GobiernoUSA.gov
• Update of CVM's What's New - Traveling to the Heartland to Discuss Antimicrobial Resistance, U.S. Food & Drug Administration (FDA)
• Harveys and Winn-Dixie Recall Various Bakery Oatmeal Raisin Cookie Products, U.S. Food & Drug Administration (FDA)
• Stop & Shop Alerts Customers To Voluntary Recall Of Nature's Promise Organic Edamame, U.S. Food & Drug Administration (FDA)
• Giant Food Alerts Customers To Voluntary Recall Of Nature's Promise Organic Edamame, U.S. Food & Drug Administration (FDA)
• Giant/Martin's Alerts Customers To Voluntary Recall Of Nature's Promise Organic Edamame, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Food Safety Modernization Act, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - November 2, 2015, U.S. Food & Drug Administration (FDA)
• Farmer Creek is Issuing a Voluntary Recall on Canned Albacore Tuna Products because of a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Northstar Produce Inc. Recalls Granny Smith Size 175 Apples Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Kar's Nuts Recalling Certain Packages of Sweet 'N Salty Mix, U.S. Food & Drug Administration (FDA)
• Hormel Foods Sales LLC Voluntarily Recalls a Limited Number of Jars of Skippy Reduced Fat Creamy Peanut Butter Spread Due to Possible Metal Pieces, U.S. Food & Drug Administration (FDA)
• National Video Supply Issues Voluntary Nationwide Recall of All Lots of Rhino 7 3000 and Rhino 7 Platinum 3000 Capsules due to Undeclared Active Pharmaceutical Ingredients, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Guidance on Investigational New Drug Applications, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 28, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Myocardial Protection System (MPS) Delivery Sets by Quest Medical: Recall - Intermittent Seal Failure During Use, FDA MedWatch
• Quest Medical, Inc. Issues Recall of MPS® Delivery Set, U.S. Food & Drug Administration (FDA)
• FDA takes enforcement action against retailers who have repeatedly sold tobacco products to minors, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Auvi-Q (epinephrine injection, USP): Recall - Potential Inaccurate Dosage Delivery, FDA MedWatch
• Helados La Tapatìa, Inc. Retira productos debido a Alérgenos Posibles, U.S. Food & Drug Administration (FDA)
• Sanofi US Issues Voluntary Nationwide Recall of Auvi-Q® Due to Potential Inaccurate Dosage Delivery, U.S. Food & Drug Administration (FDA)
• Premiere Sales Group Issues Voluntary Nationwide Recall of All Lots of Rhino 7 3000 and Rhino 7 Platinum 3000 Capsules due to Undeclared Active Pharmaceutical Ingredients, U.S. Food & Drug Administration (FDA)
• Herr's Announces Voluntary Recall of Select Bags of 1.875 oz. Sour Cream and Onion Potato Chips with Packaging Error, U.S. Food & Drug Administration (FDA)
• Sockeye Suzy's Fish Co Issuing A Voluntary Recall On All Canned Seafood Products Because Of A Possible Health Risk, U.S. Food & Drug Administration (FDA)
• CSFPDX Of Garibaldi, Oregon Is Issuing A Voluntary Recall On All 64 oz. (4Lbs.) Canned Wild Albacore Tuna Because Of A Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Helados La Tapatia, Inc. Recalls Products Because of Possible Allergens, U.S. Food & Drug Administration (FDA)
• Gilmore Fish Smokehouse Is Issuing A Voluntary Recall On All Canned Sturgeon And Salmon Products Because Of A Possible Health Risk, U.S. Food & Drug Administration (FDA)
• OleBob's Seafoods Canned Seafood Recall, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Dairy Groups Exporting to China Face New Requirements, U.S. Food & Drug Administration (FDA)
• Parents & Party Hosts: Your Halloween Guide to Food Safety, FoodSafety.gov
• Josephson's Smokehouse Aids In Seafood Recall, U.S. Food & Drug Administration (FDA)
• Skinny Latina Foods, Inc. Issues Recall for Undeclared Soy, U.S. Food & Drug Administration (FDA)
• Kanan Enterprises Conducts Nationwide Voluntary Recall of Certain Products Containing Candy Buttons, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Salix Animal Health, LLC, Expands Voluntary Recall of Good N Fun Beefhide Chicken Sticks Dog Treats Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Entacapone: Drug Safety Communication - FDA Review Found No Increased Cardiovascular Risks, FDA MedWatch
• Ethereal Confections Issues Allergy Alert On Undeclared Amounts Of Milk In Chocolates, U.S. Food & Drug Administration (FDA)
• Salix Animal Health, LLC, Expands Voluntary Recall of Good N Fun Beefhide Chicken Sticks Dog Treats Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Curry Chicken Salad and Classic Deli Pasta Salad in Seven States Due to Possible Listeria Contamination, U.S. Food & Drug Administration (FDA)
• David Trail Mix Sweet & Salty Voluntarily Recalled Due To Undeclared Dairy Allergen, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 21, 2015, U.S. Food & Drug Administration (FDA)
• Seaquest Seafood Corp. Recalling Dehydrated & Marinated Uneviscerated Fish because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Treating Cushing's Disease in Dogs, U.S. Food & Drug Administration (FDA)
• FDA Drug Safety Communication: FDA warns of serious liver injury risk with hepatitis C treatments Viekira Pak and Technivie, U.S. Food & Drug Administration (FDA)
• Ya comenzó el periodo de inscripción para la Lotería de Visas, GobiernoUSA.gov
• FDA MedWatch - Hepatitis C Treatments Viekira Pak and Technivie: Drug Safety Communication - Risk of Serious Liver Injury, FDA MedWatch
• FDA MedWatch - Kayexalate (sodium polystyrene sulfonate): Drug Safety Communication - FDA Requires Drug Interaction Studies, FDA MedWatch
• FDA approves new treatment for advanced pancreatic cancer, U.S. Food & Drug Administration (FDA)
• The Spot is Issuing a Voluntary Recall on All Canned Seafood Products Because of a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• VIS Seafoods is Issuing a Voluntary Recall on All Canned Salmon Products Because of a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Brigham Fish Market is Voluntarily Recalling Canned Seafood Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Dungeness Seaworks is Voluntarily Recalling all Canned Seafood Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• US Marshals seize adulterated crab products for food safety violations, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Downing Labs, LLC Sterile Compounded Products: Recall - Lack of Sterility Assurance, FDA MedWatch
• Downing Labs, LLC Issues Voluntary Nationwide Recall of All Sterile Compounded Products Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• FDA approves first Factor X concentrate to treat patients with rare hereditary bleeding disorder, U.S. Food & Drug Administration (FDA)
• Northwest Wild Products is Issuing a Voluntary Recall on all Canned Seafood Products Because of a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Cómo conseguir cobertura médica para el próximo año, GobiernoUSA.gov
• Enforcement Report for October 14, 2015, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - NFL Comment Period Reopening, U.S. Food & Drug Administration (FDA)
• P. East Trading Corp Distributors Issues an Alert on Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• Bornstein Seafood, Inc is Voluntarily Recalling all Canned Seafood Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Re: Pacific Oyster Company D/B/A The Fish Peddler Of Bay City, Oregon, Is Voluntarily Recalling Canned Tuna, Salmon, And Smoked Salmon, U.S. Food & Drug Administration (FDA)
• Notice of Voluntary Recall of Certain Martinelli's 8.4 oz. Sparkling Beverages Due to Potential for Glass Fragments, U.S. Food & Drug Administration (FDA)
• FDA approves Praxbind, the first reversal agent for the anticoagulant Pradaxa, U.S. Food & Drug Administration (FDA)
• The Garibaldi Cannery LLC is Issuing a Voluntary Recall on all Canned Seafood Products Because of a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Ecola Seafoods Inc. is Issuing a Voluntary Recall on all Canned Salmon and Tuna Because of a Possible Health Risk, U.S. Food & Drug Administration (FDA)
• 7 Ways to Celebrate National Mammography Day, FDA Office of Women's Health
• CVM Updates - FDA Issues Final Guidance to Help Evaluate Effectiveness of Drugs to Reduce Pathogenic Shiga Toxin-Producing E. coli in Cattle, U.S. Food & Drug Administration (FDA)
• A&S Food Trading Inc Issues Alert on Undeclared Sulfites in Gorgeous Memory Daylily, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Heater-Cooler Devices: FDA Safety Communication - Use of Devices Associated With Nontuberculous Mycobacteria Infections, FDA MedWatch
• Del Monte Fresh Produce N.A. Inc., Recalls Limited Quantity of Fresh Apples Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Del Monte Fresh Produce N.A. Inc., Recalls Limited Quantity of "Fresco Fresh" Brand Parfait Yogurt Cups Due to Undeclared Tree Nut Allergen, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Nontuberculous Mycobacterium Infections Associated with Heater-Cooler Devices: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Asunto: Alertas y regulaciones de viaje para pasajeros, GobiernoUSA.gov
• CFSAN Constituent Update - REGULATIONS.GOV Technical Difficulties, U.S. Food & Drug Administration (FDA)
• Medline Industries, Inc. Issues A Voluntary Nationwide Recall Of One Lot Of Acetaminophen Tablets, 500mg, Due To Mislabeling With Incorrect Strength, U.S. Food & Drug Administration (FDA)
• Nijay International, Inc. Recalls Coriander Powder Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Acetaminophen Tablets by Medline Industries: Recall - Mislabeling with Incorrect Strength, FDA MedWatch
• Market of Choice Recalls Baked Brie Herb-Garlic Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Dole Fresh Vegetables Announces Precautionary Recall of Limited Number of Spinach Salads, U.S. Food & Drug Administration (FDA)
• New Frontier Foods, Inc. Issues Voluntary Recall Of Ocean's Halo Seaweed Chips Produced At Third Party Manufacturer On Certain Dates, Because Of Possible Health Risk (Undeclared Allergen - Wheat), U.S. Food & Drug Administration (FDA)
• Cook Medical Expands Global Recall of Select Sizes of Beacon Tip Angiographic Catheters, U.S. Food & Drug Administration (FDA)
• Skipanon Brand Seafoods LLC Recalls all Seafood Canned Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 07, 2015, U.S. Food & Drug Administration (FDA)
• TF Supplements Issues Voluntary Nationwide Recall of All Lots of Rhino 7 3000 and Rhino 7 Platinum 3000 Capsules due to Undeclared Active Pharmaceutical Ingredients, U.S. Food & Drug Administration (FDA)
• Violencia doméstica: qué puede hacer para protegerse, GobiernoUSA.gov
• FDA expands approved use of Opdivo in advanced lung cancer, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - September 2015 Drug Safety Labeling Changes includes 48 products with revisions to Prescribing Information, FDA MedWatch
• Tristar Food Wholesale Co. Inc. Issues Allergy Alert On Undeclared Sulfites In Heng Cheong Loong Co. Golden Raisins, U.S. Food & Drug Administration (FDA)
• American Pure Whey Issues Allergy Alert on Undeclared Milk and Soy in Whey Protein Products, U.S. Food & Drug Administration (FDA)
• October - Women's Health Update, FDA Office of Women's Health
• Whole Foods Market Voluntarily Recalls All Cut, Wrapped And Weighed Papillion Organic Roquefort Cheeses Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• New England Natural Bakers Inc. Issues Voluntary Allergy Alert on Undeclared Milk Wheat and Tree Nuts (Pecans) in Coconut Cranberry Granola, U.S. Food & Drug Administration (FDA)
• Conozca cómo identificar las estafas piramidales, GobiernoUSA.gov
• Federal judge issues permanent injunction against South Dakota laser manufacturer, U.S. Food & Drug Administration (FDA)
• General Mills Issues Voluntary Recall Of Cheerios And Honey Nut Cheerios Cereal Produced At Its Lodi, California Location On Certain Dates, U.S. Food & Drug Administration (FDA)
• Snack Out Loud Foods Issues Allergy Alert On Undeclared Milk In Snack Out Loud Sea Salt Crunchy Bean Snacks 1.2oz Single Serve Units, U.S. Food & Drug Administration (FDA)
• General Mills Voluntarily Recalls a Limited Quantity of Frozen Cascadian Farm Cut Green Beans, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA’s Strategy for FSMA Training: Public and Private Partners Working Together, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FSMA Training, U.S. Food & Drug Administration (FDA)
• Olysio (simeprevir) label revised, U.S. Food & Drug Administration (FDA)
• FDA launches national public education campaign to prevent and reduce tobacco use among multicultural youth, U.S. Food & Drug Administration (FDA)
• FDA approves new injectable drug to treat schizophrenia, U.S. Food & Drug Administration (FDA)
• FDA approves expanded indication for medical device to treat a form of brain cancer, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Bioprosthetic Aortic Valves: FDA Notification - Reduced Leaflet Motion, FDA MedWatch
• CFSAN Constituent Update - FDA Makes Available New Food Related Emergency Exercises, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - K-9 Kraving Dog Food Has Announced a Voluntary Recall of Their Chicken Patties Dog Food Shipped Between July 13th - July 17th, 2015, U.S. Food & Drug Administration (FDA)
• K-9 Kraving Dog Food Has Announced a Voluntary Recall of Their Chicken Patties Dog Food Shipped Between July 13th - July 17th, 2015 Because The Product May Be Contaminated With Salmonella and Listeria monocytogenes, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA to Improve Process Used by Food Processors to Submit Information to FDA on Acidified and Low Acid Canned Food, U.S. Food & Drug Administration (FDA)
• FDA orders duodenoscope manufacturers to conduct postmarket surveillance studies in health care facilities, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: MicroPort Orthopedics Inc., PROFEMUR Neck Varus/Valgus CoCr 8 Degree, Part number PHAC 1254, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Drug Products Intended to be Sterile by Chen Shwezin Inc., dba Park Compounding Pharmacy: FDA Statement - Lack of Sterility Assurance, FDA MedWatch
• Texas Star Nut and Food Co., Inc. Voluntarily Recalls Natural Macadamia Nuts and Simply Raw Trail Mix Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Dean Foods of Decatur, Ind. Issues Allergy Alert On Undeclared Milk in Sunkist Frozen Mango Fruit Sorbet Bars, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - PROFEMUR Neck Varus/Valgus CoCr 8 Degree, Part number PHAC 1254 by MicroPort Orthopedics: Class I Recall - Unexpected Rate of Fractures After Surgery, FDA MedWatch
• FDA approves Keytruda for advanced non-small cell lung cancer, U.S. Food & Drug Administration (FDA)
• Únase a la charla sobre el cáncer de seno (mama) el 6 de octubre, GobiernoUSA.gov
  • <Possible follow-ups>
  • Únase a la charla sobre el cáncer de seno (mama) el 6 de octubre, GobiernoUSA.gov
• Wyandot Inc. Issues Allergy Alert on Undeclared Milk in Yellow Round Tortillas, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals October 2015 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Salix Animal Health, LLC, Announces Voluntary Recall of One Lot of "Good 'N' Fun - Beefhide Chicken Sticks" Dog Treats Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Press Release For Voluntary Recall of Kermit, Inc. Products, U.S. Food & Drug Administration (FDA)
• Salix Animal Health, LLC, Announces Voluntary Recall of One Lot of "Good 'N' Fun - Beefhide Chicken Sticks" Dog Treats Due to Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• Fatima Brothers Issues Alert On Undeclared Sulfites In Shad Raisins, U.S. Food & Drug Administration (FDA)
• United TC Issues Allergy Alert on Undeclared Sulfites in Golden Raisins, U.S. Food & Drug Administration (FDA)
• Apoyo para quienes cuidan de una persona con Alzheimer, GobiernoUSA.gov
• Hágase la prueba de colesterol, GobiernoUSA.gov
• Update of CVM's What's New - For Veterinarians, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Revised Guidance on Veterinary Feed Directive Regulation Questions and Answers, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cranial Perforators With an Automatic Clutch Mechanism: Safety Communication - Failure to Disengage, FDA MedWatch
• FDA Safety Communication: Cranial Perforators with an Automatic Clutch Mechanism, Failure to Disengage, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - OC RAW DOG Voluntarily Recalls Limited Number of Raw Frozen Dog Food Due to Potential Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Federal judge enters permanent injunction against Florida dietary supplements maker, Sunset Natural Products Inc., U.S. Food & Drug Administration (FDA)
• OC RAW DOG Voluntarily Recalls Limited Number of Raw Frozen Dog Food Due to Potential Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 23, 2015, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Western Milling LLC Voluntarily Recalls Western Blend Horse Feed, Lot 5251 Due To Potential Monensin Contamination, U.S. Food & Drug Administration (FDA)
• TF Supplements Issues Voluntary Nationwide Recall of Dietary Supplements with Undeclared Active Pharmaceutical Ingredients, U.S. Food & Drug Administration (FDA)
• Western Milling LLC Voluntarily Recalls Western Blend Horse Feed, Lot 5251 due to potential Monensin contamination., U.S. Food & Drug Administration (FDA)
• Truco Enterprises Recalls 18oz Cafe Style Tortilla Chips Due To The Possible Presence Of Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• Mr. Goodcents Franchise Systems, Inc. Voluntarily Issues Allergy Alert On Undeclared Peanuts In A Chocolate Chip Cookie, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Presentations Now Available, U.S. Food & Drug Administration (FDA)
• Reyataz (atazanavir) oral powder label updated, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Murphy Farm Hay and Feed Company Issues Recall of Alfalfa Hay Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Murphy Farm Hay and Feed Company Issues Recall of Alfalfa Hay Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• El asma y la actividad física en la escuela, GobiernoUSA.gov
• Tastee Apple, Inc., Issues Allergy Alert On Undeclared Peanuts In Plain Caramel Apples, U.S. Food & Drug Administration (FDA)
• Greencore, USA - Rhode Island, Issues Allergy Alert Due to the Potential for Undeclared Almonds in Evolution Fresh Nonfat Greek Yogurt with Strawberry and Granola Parfaits Sold in 266 Locations in Massachusetts, Rhode Island, New Hampshire, New York, Connecticut, Vermont and Maine, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sterile Compounded Products by US Compounding, Inc: Recall - Lack of Sterility Assurance, FDA MedWatch
• US Compounding, Inc. Issues Voluntary Nationwide Recall of All Sterile Compounded Products, U.S. Food & Drug Administration (FDA)
• Lucy's Weight Loss System Issues Voluntary Nationwide Recall of Pink Bikini and Shorts on The Beach Due to Undeclared Sibutramine and Phenolphthalein, U.S. Food & Drug Administration (FDA)
• Es posible pagar las tarifas de naturalización con su tarjeta de crédito, GobiernoUSA.gov
• Día Nacional de Registro de Votantes, GobiernoUSA.gov
• Update of CVM's What's New - "I and love and you" Expands Voluntary Recall of Beef Gullet Strips Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• "I and love and you" Expands Voluntary Recall of Beef Gullet Strips Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Picnic Gourmet Spreads Issues Recall for Potential Health Risks, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Avycaz (ceftazidime and avibactam): Drug Safety Communication - Dose Confusion and Medication Errors, FDA MedWatch
• Update of CVM's What's New - New Videos for Reporting Problems with Animal Food, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tramadol: Drug Safety Communication - FDA Evaluating Risks of Using in Children Aged 17 and Younger, FDA MedWatch
• Update of CVM's What's New - FDA Holding Public Meeting on FSMA Preventive Controls for Human and Animal Food Final Rules, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Freedom Driver System by SynCardia: Class I Recall - Part May Fail Causing Device to Stop Working, FDA MedWatch
• Medical Device Safety and Recalls: SynCardia Systems, Freedom Driver System - Part May Fail Causing Device to Stop Working, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Basics Webinar, U.S. Food & Drug Administration (FDA)
• Celebrate Hispanic Heritage Month with FoodSafety.gov, FoodSafety.gov
• CVM Updates - FDA, USDA, and CDC Holding Public Meeting on On-Farm Antimicrobial Use Data Collection, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Antiparasitic Drugs Needed for Small Ruminants, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ayurvedic Dietary Supplements by Shree Baidyanath: Consumer Advice Notice - Products Contain High Levels of Lead and/or Mercury, FDA MedWatch
• Butala Emporium, Inc. Recalls Eleven Ayurvedic Dietary Supplements Because of Elevated Levels of Lead and Mercury, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Consumer Advice on Shree Baidyanath Brand Ayurvedic Dietary Supplements, U.S. Food & Drug Administration (FDA)
• Karoun Dairies, Inc. Issues Nationwide Voluntary Recall of Various Cheeses Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Infections Associated with Reprocessed Flexible Bronchoscopes - FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Reprocessed Flexible Bronchoscopes: FDA Safety Communication - Risk of Infection, FDA MedWatch
• September Women's Health Update: FDA Office of Women's Health, FDA Office of Women's Health
• FDA MedWatch - HeartMate II Left Ventricular Assist System (LVAS) by Thoratec Corporation: Urgent Medical Device Correction - Monitor the Backup Battery Expiration Date, FDA MedWatch
• Potential Health Hazard: Recalled Snack Fresh Brand Red Apple Slices May Have Been Distributed To Florida's Palm Beach County School District, U.S. Food & Drug Administration (FDA)
• Thoratec Issues Voluntary Device Correction, U.S. Food & Drug Administration (FDA)
• Iowa Select Herbs, LLC Issues a Nationwide Recall of Its Products Pursuant to Consent Decree Issued by the Federal Court for the Northern District of Iowa, U.S. Food & Drug Administration (FDA)
• Celebremos el Mes de la Herencia Hispana, GobiernoUSA.gov
• FDA MedWatch - Clozapine: Drug Safety Communication - FDA Modifies Monitoring for Neutropenia; Approves New Shared REMS Program, FDA MedWatch
• CFSAN Constituent Update - Commenting on Menu Labeling Guidance, U.S. Food & Drug Administration (FDA)
• FDA issues orders that will stop further U.S. sale and distribution of four R.J. Reynolds Tobacco Company cigarette products, U.S. Food & Drug Administration (FDA)
• Custom Produce Sales Voluntarily Recalls Fat Boy Brand® and Unlabeled Cucumbers Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Limited Precautionary Recall of 5 oz organicgirl Baby Spinach Announced, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 09, 2015, U.S. Food & Drug Administration (FDA)
• Custom Prodouce Sales Voluntarily Recalls Fat Boy Brand® and Unlabeled Cucumbers Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• The One Minute Miracle Inc. Issues Voluntary Nationwide Recall of MIRACLE DIET 30 Due to Presence of Undeclared Phenolphthalein and MIRACLE ROCK 48 Due to Presence of Undeclared Thiosildenafil, U.S. Food & Drug Administration (FDA)
• Desastres: Tenga un plan | Prepare un equipo | Esté informado, GobiernoUSA.gov
• CFSAN Constituent Update - Menu Labeling Guidance, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - 2015 Voluntary National Retail Food Regulatory Program Standards, U.S. Food & Drug Administration (FDA)
• FDA Announces Medistat RX's Nationwide Voluntary Recall of Sterile Drug Products, U.S. Food & Drug Administration (FDA)
• Appeeling Fruit Inc. Voluntarily Recalls Limited Production Of, U.S. Food & Drug Administration (FDA)
• Anhing Corporation Announces Recall of ABC Shaped Cookies Banh Chu, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Insulet Corporation, OmniPod Insulin Management System May Fail to Deliver Insulin, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Invokana and Invokamet (canagliflozin): Drug Safety Communication - New Information on Bone Fracture Risk and Decreased Bone Mineral Density, FDA MedWatch
• Update of CVM's What's New - FSMA Final Rule for Preventative Controls for Animal Food, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medistat RX Sterile Drug Products: Recall - Possible Contamination, FDA MedWatch
• Nine Alaska Safeway and Carrs Stores Voluntarily Recall Deli Sandwiches Containing Cucumbers in Cooperation with the Andrew and Williamson Fresh Produce Recall Due to Possible Salmonella Poona Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - August 2015 Safety Labeling Changes includes 43 products with revisions to Prescribing Information, FDA MedWatch
• Pop Quiz: What Do You Know About Food Safety?, FoodSafety.gov
• The Kraft Heinz Company Expands Voluntary Recall of Wrapped American Slices, U.S. Food & Drug Administration (FDA)
• Okarche Bakery, Issues Allergy Alert on Undeclared Milk, Soy, Wheat and Yellow #5 in Frozen Cookie Dough, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues Draft Guidance on Distributor Labeling for New Animal Drugs, U.S. Food & Drug Administration (FDA)
• CVM Updates - Fees Announced to Support Export Certificate Program, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Compounded or Repackaged Drugs Stored in Becton-Dickinson Syringes: FDA Expands Warning, FDA MedWatch
• The September 2015 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - new email alert service, U.S. Food & Drug Administration (FDA)
• Andrew and Williamson Fresh Produce Recalls Limited Edition Brand Cucumbers Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Food Nation Issues Alert on Undeclared Sulfites in "Western Beef Packaged of Sun Dried Tomatoes", U.S. Food & Drug Administration (FDA)
• Best Cash & Carry Recalls Rose Brand Cranberry Mix Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 02, 2015, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals September 2015 Update, U.S. Food & Drug Administration (FDA)
• Día del Trabajo - 7 de septiembre, GobiernoUSA.gov
• H-E-B Issues A Voluntary Recall On Hill Country Fare One Gallon Spring Water Due To The Possible Presence Of Undeclared Allergen, U.S. Food & Drug Administration (FDA)
• 4 Myths About the Food in Your Fridge, FoodSafety.gov
• Sincerely Nuts Recalls Raw Macadamia Nuts Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• ¿Qué es un poder legal?, GobiernoUSA.gov
• Medical Device Safety and Recalls: Covidien, Puritan Bennett 980 Ventilators - Amount of Air Delivered May Be Lower Than Programmed, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Dräger Medical, Evita V500 and Babylog VN500 Ventilators - Faulty Batteries, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: CareFusion Alaris Syringe Pump Alarm Error May Cause Interruption of Therapy, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Puritan Bennett 980 Ventilators by Covidien: Class I Recall - Amount of Air Delivered May Be Lower Than Programmed, FDA MedWatch
• FDA MedWatch - Evita V500 and Babylog VN500 Ventilators by Dräger Medical: Class I Recall - Faulty Batteries, FDA MedWatch
• FDA approves new drug treatment for nausea and vomiting from chemotherapy, U.S. Food & Drug Administration (FDA)
• ¡A su salud! Ordene GRATIS 10 publicaciones para mujeres adultas, GobiernoUSA.gov
• Enforcement Report for August 26, 2015, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Pure Powdered Caffeine Products, U.S. Food & Drug Administration (FDA)
• VRVK Nutraceuticals, LLC Issues Allergy Alert on Undeclared Crustacean Shellfish and Milk in Two Lots of Ultimate Antioxidant Tablets, U.S. Food & Drug Administration (FDA)
• Bonduelle USA Recalls Frozen Corn Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FSMA Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - FSMA Update, U.S. Food & Drug Administration (FDA)
• Tasty Delicious Bakery Inc. Issues Allergy Alert On Undeclared Eggs In Sugar Bun, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - DPP-4 Inhibitors for Type 2 Diabetes: Drug Safety Communication - May Cause Severe Joint Pain, FDA MedWatch
• FDA MedWatch - OmniPod (Pod) Insulin Management System by Insulet Corporation: Recall - Possibility of a Higher Rate of Failure, FDA MedWatch
• Insulet Corporation Issues Voluntary Recall of OmniPod Insulin Management System, U.S. Food & Drug Administration (FDA)
• The One Minute Miracle Inc. Issues Voluntary Nationwide Recall of MIRACLE DIET 30 Due to Presence of Undeclared Phenolphthalein & MIRACLE ROCK 48 Due to Presence of Undeclared Thiosildenafil, U.S. Food & Drug Administration (FDA)
• FDA approves Repatha to treat certain patients with high cholesterol, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Alaris Syringe Pump by CareFusion: Class I Recall - Alarm Error May Cause Interruption of Therapy, FDA MedWatch
• FDA MedWatch - Alaris Medley Large Volume Pump (LVP) Frame Membrane by Elite Biomedical Solutions: Class I Recall - Frame Membrane May Allow Over or Under Delivery of Fluid by an Infusion Pump, FDA MedWatch
• Medical Device Safety and Recalls: CareFusion Alaris Syringe Pump, Alarm Error May Cause Interruption of Therapy, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Elite Biomedical Solutions, Alaris Medley Large Volume Pump (LVP) Frame Membrane, Frame Membrane May Allow Over or Under Delivery of Fluid by an Infusion Pump, U.S. Food & Drug Administration (FDA)
• Bimbo Bakeries Voluntary Regional Recall of Certain Limited Breads Produced Under the Sara Lee, Great Value, Kroger, Bimbo, Nature’s Harvest and L’Oven Fresh Brands, U.S. Food & Drug Administration (FDA)
• FDA takes action against three tobacco manufacturers for making “additive-free” and/or “natural” claims on cigarette labeling, U.S. Food & Drug Administration (FDA)
• Edurant (rilpivirine) labeling updated, U.S. Food & Drug Administration (FDA)
• General Mills voluntarily recalls a limited quantity of frozen Cascadian Farm Cut Green Beans, U.S. Food & Drug Administration (FDA)
• Recall Sam Mills Gluten Free Chocolate Chip Granola Bar, U.S. Food & Drug Administration (FDA)
• Sid Wainer and Son Recalls Jansal Valley Raw Macadamia Nuts Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Novacare, LLC Issues Voluntary Nationwide Recall of Dietary Supplements Due to Undeclared Salicylic Acid, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hudson RCI Sheridan Sher-I-Bronch Endobroncial Tube by Teleflex Medical: Class I Recall - Connector May Crack or Separate, FDA MedWatch
• FDA Basics Webinar- August 31: Food Safety: Bad Weather Basics, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Teleflex Medical, Hudson RCI Sheridan Sher-I-Bronch Endobronchial Tube - Connector May Crack or Separate, U.S. Food & Drug Administration (FDA)
• ¿Se ha inscrito para votar en su estado?, GobiernoUSA.gov
• Jo’s Candies Issues Voluntary Alert on Undeclared Milk in, U.S. Food & Drug Administration (FDA)
• Allergan Issues Voluntary Nationwide Recall In The U.S. Of Specific Lots Of REFRESH&reg; Lacri-Lube&reg;, REFRESH P.M. &reg;,, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Refresh Lacri-Lube, Refresh P.M., FML 0.1 Percent and Blephamide 10 Percent/0.2 Percent by Allergan: Recall - Particulate Matter, FDA MedWatch
• Aprenda cómo prevenir la diabetes este miércoles, GobiernoUSA.gov
• CVM Updates - FDA Releases Biannual Progress Report, Announces Public Meeting on Use of Antimicrobials in Food-producing Animals, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Picato (ingenol mebutate) Gel: Drug Safety Communication - FDA Warns of Severe Adverse Events, Requires Label Changes, FDA MedWatch
• Back-to-School Food Safety Tips for Parents & Caregivers, FoodSafety.gov
• Chetak New York L.L.C. Recalls 14.1 oz. Jar of "Deep Coriander Powder" Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Intoxicaciones con alimentos, GobiernoUSA.gov
• CVM Updates - FDA Seeks Public Comments on Approval Process for Combination Drug Medicated Feeds, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CVM Updates - FDA Seeks Public Comments on Approval Process for Combination Drug Medicated Feeds, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 19, 2015, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Makes Available 18 Years of NARMS Isolate-level Data on Enteric Bacterial Isolates, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 12, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Compounded Drugs Stored in Becton-Dickinson (BD) 3 ml and 5 ml Syringes: FDA Warning - Do Not Use, FDA MedWatch
• FDA approves first treatment for sexual desire disorder, U.S. Food & Drug Administration (FDA)
• August Women's Health Update, FDA Office of Women's Health
• FDA MedWatch - OxyTOTE Portable Oxygen Unit by Western/Scott Fetzer Company: Class I Recall - May Ignite and Burst, FDA MedWatch
• FDA MedWatch - Prolotherapy with Phenol by Hartley Medical: Recall - Non-sterility Concerns, FDA MedWatch
• Blue Square Market Issues Update to Voluntary Nationwide Recall of Kaboom Action Strips and Lida Daidaihua Due to the Presence of Undeclared Sulfoaildenafil, Sibutramine and Phenolphthalein, U.S. Food & Drug Administration (FDA)
• Hartley Medical Issues Voluntary Recall of Prolotherapy with Phenol Due to Non-sterility Concerns, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Western/Scott Fetzer Company OxyTOTE Portable Oxygen Unit May Ignite and Burst, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Mammograms at Boston Diagnostic Imaging in Orlanda, Florida: FDA Safety Communication - Quality Problems, FDA MedWatch
• Medical Device Safety: Problem with Quality of Mammograms at Boston Diagnostic Imaging in Orlando, Florida: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Quejas por discriminación al buscar una vivienda, GobiernoUSA.gov
• FDA MedWatch - July 2015 Safety Labeling Changes includes 49 products with revisions to Prescribing Information, FDA MedWatch
• Update of CVM's What's New - Draft Guidance on Animal Drug Compounding from Bulk Drug Substances – comment period extended to November 16, 2015, U.S. Food & Drug Administration (FDA)
• ¿Comer más y bajar de peso?, GobiernoUSA.gov
• UPDATED - Allergy Alert on Undeclared Milk in Nutrition Resource Services, Inc.'s Whey, Casein, and Colostrum Protein Products, U.S. Food & Drug Administration (FDA)
• 10 consejos para un regreso a clases organizado y seguro, GobiernoUSA.gov
• Good Seed Inc. Recalls Soybean Sprouts & Mung Bean Sprouts Due To A Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Northwest Farm Food Cooperative Voluntarily Recalls Frozen Raw Cat Food Due To Possible Salmonella Contamination, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Releases 2012 and 2013 NARMS Integrated Annual Report, U.S. Food & Drug Administration (FDA)
• Kent, Washington Firm Issues Allergy Alert On Undeclared Peanut Ingredients, U.S. Food & Drug Administration (FDA)
• NORTHWEST FARM FOOD COOPERATIVE VOLUNTARILY RECALLS FROZEN RAW CAT FOOD DUE TO POSSIBLE SALMONELLA CONTAMINATION, U.S. Food & Drug Administration (FDA)
• Blue Square Market Issues Voluntary Nationwide Recall of Kaboom Action Strips and Lida Daidaihua Due to the Presence Of Undeclared Sulfoaildenafil, Sibutramine And Phenolphthalein, U.S. Food & Drug Administration (FDA)
• Voluntary Nationwide Recall Of Grey Wash Tattoo Inks And Tattoo Kits by Thousand Virgins Corp Due To Microbial Contamination, U.S. Food & Drug Administration (FDA)
• Mahina Mele Farm Recalls Their Macadamia Nut Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Voluntary Nationwide Recall Of A Thousand Virgins Grey Wash Tattoo Inks And Tattoo Kits Due To Microbial Contamination, U.S. Food & Drug Administration (FDA)
• Cook Medical Issues Global Recall Of Beacon Tip Angiographic Catheter Products, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Cook Medical Issues Global Recall Of Beacon Tip Angiographic Catheter Products, U.S. Food & Drug Administration (FDA)
• Angry Orchard Cider Company Announces Voluntary Recall of Select Cases of Angry Orchard Crisp Apple Hard Cider, U.S. Food & Drug Administration (FDA)
• Vacunas, nuestra mejor defensa, GobiernoUSA.gov
• FDA MedWatch - Beacon Tip Angiographic Catheters by Cook Medical: Class 1 Recall - Catheter Tip May Slip or Separate, FDA MedWatch
• Medical Device Safety and Recalls: Cook Medical, Beacon Tip Angiographic Catheters, Catheter Tip May Slip or Separate, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - FDA Warns Tattoo Artists and Consumers Not to Use Certain Tattoo Inks, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals August 2015 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Tivicay (dolutegravir) and Triumeq (abacavir/dolutegravir/lamivudine) product labeling was updated, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Serious Adverse Events with Implantable Left Ventricular Assist Devices (LVADs): FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Implantable Left Ventricular Assist Devices (LVADs): FDA Safety Communication - Serious Adverse Events, FDA MedWatch
• CVM Updates - FDA reissuing draft guidance for human and animal drug manufacturers on Disclosing Risk Information in Consumer-Directed Print Advertisements and Promotional Labeling for Prescription Drugs, U.S. Food & Drug Administration (FDA)
• The August 2015 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Gilenya (fingolimod): Drug Safety Communication - FDA Warns About Cases of Rare Brain Infection, FDA MedWatch
• Medical Device Safety and Recalls: Supplemental Measures to Enhance Duodenoscope Reprocessing: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Duodenoscope Reprocessing: FDA Safety Communication - Supplemental Measures to Enhance Reprocessing, FDA MedWatch
• CVM Updates - FDA Issues Guidance on the Use of Nanomaterials in Food for Animals, U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - August 3, 2015, U.S. Food & Drug Administration (FDA)
• Kilwin's Quality Confections, Inc. Issues Allergy Alert on Undeclared Cashew in Sugar Free Milk Chocolate Caramels, U.S. Food & Drug Administration (FDA)
• The Kraft Heinz Company Voluntarily Recalls Select Varieties of Kraft Singles Products Due to Potential Choking Hazard, U.S. Food & Drug Administration (FDA)
• Allergy Alert On Undeclared Milk In Nutrition Resource Services, Inc.'s Whey, Casein, And Colostrum Protein Products, U.S. Food & Drug Administration (FDA)
• Unichem Pharmaceuticals (USA), Inc. Issues a Voluntary Nationwide Recall of Hydrochlorothiazide Tablets Due to the Potential Presence of Foreign Tablets, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Coconut Curry Cauliflower Salad in Twenty-one Stores Due to Undeclared Almonds, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 29, 2015, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hydrochlorothiazide Tablets by Unichem Pharmaceuticals (USA), Inc: Recall - Potential Presence of Foreign Tablets Contamination, FDA MedWatch
• FDA MedWatch - Symbiq Infusion System by Hospira: FDA Safety Communication - Cybersecurity Vulnerabilities, FDA MedWatch
• John B. Sanfilippo & Son, Inc. Voluntarily Recalls Fisher Brand 10 Ounce Chopped Walnuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Cybersecurity Vulnerabilities of Hospira Symbiq Infusion System: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 0.9 Percent Sodium Chloride Injection, USP (AUTO-C) by Baxter International: Recall - Potential For Leaking Containers, Particulate Matter and Missing Port, FDA MedWatch
• Baxter Initiates Voluntary Nationwide Recall Of One Lot Of Iv Solution Due To The Potential For Leaking Containers, Particulate Matter And Missing Port Protectors, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Baxter Initiates Voluntary Nationwide Recall of One Lot of IV Solution Due to the Potential For Leaking Containers, Particulate Matter and Missing Port Protectors, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Raw Milk Cheese Data Call and Joint FDA/Health Canada Risk Assessment, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces FY 2016 Animal Drug User Fee Rates for ADUFA and AGDUFA, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Brintellix (vortioxetine) and Brilinta (ticagrelor): Drug Safety Communication - Name Confusion, FDA MedWatch
• Update of CVM's What's New - Final Guidance Available, U.S. Food & Drug Administration (FDA)
• ¿Listo para regresar a la escuela? ¡Aproveche los días sin impuesto estatal!, GobiernoUSA.gov
• Update of CVM's What's New - New Video - U.S. Measures to Protect Against BSE, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Information about the Large Volume Intravenous (IV) Solution Shortage, U.S. Food & Drug Administration (FDA)
• Kroger Recalls Four Seasonings Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• KellBran Candies Issues Allergy Alert on Undeclared Milk in Caramel Popcorn, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Adrucil (fluorouracil injection, USP) 5 g/100 mL (50 mg/mL) by Teva Parenteral Medicines: Recall - Particulate Matter, FDA MedWatch
• Teva Parenteral Medicines Initiates Voluntary Nationwide Recall of Select Lots of Adrucil (Fluorouracil Injection, USP) 5 G/100 mL (50 mg/mL) Due To Particulate Matter, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Gadolinium-based Contrast Agents for Magnetic Resonance Imaging (MRI): Drug Safety Communication - FDA Evaluating the Risk of Brain Deposits With Repeated Use, FDA MedWatch
• Nature's Variety Issues Nationwide Voluntary Recall of Instinct® Raw Chicken Formula Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Moses Lake Professional Pharmacy Issues Voluntary Recall of Unexpired Sterile Human and Veterinary Compounded Drugs Due to Lack of Sterility Assurance, U.S. Food & Drug Administration (FDA)
• Celebremos los 25 años de la Ley sobre Estadounidenses con Discapacidades, GobiernoUSA.gov
• FDA MedWatch - Sterile Human and Veterinary Compounded Drugs by Moses Lake Professional Pharmacy: Recall - Lack of Sterility Assurance, FDA MedWatch
• Guía para padres de niños y jóvenes en edad escolar, GobiernoUSA.gov
• FDA Hepatitis Update - Approval of Daklinza in Combination with Sofosbuvir for HCV Genotype 3 Infection, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Approval of Technivie to treat of genotype 4 chronic hepatitis C virus, U.S. Food & Drug Administration (FDA)
• Bravo Recalls Select Chicken Pet Foods Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Additional Revisions to the Nutrition Facts Label, U.S. Food & Drug Administration (FDA)
• Life & More, L.L.C. Issues Nationwide Voluntary Recall of Akttive High Performance Fat Burner Gold Capsules Due to Undeclared Drug Ingredients, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 22, 2015, U.S. Food & Drug Administration (FDA)
• FDA approves diagnostic test to differentiate between types of HIV infection, U.S. Food & Drug Administration (FDA)
• CVM Updates - New Tools Would Advance Efforts to Ensure the Safety of Imported Foods, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Safety of Imported Foods, U.S. Food & Drug Administration (FDA)
• CORRECCIÓN: ¿Necesita saber cómo abrir una cuenta bancaria o transferir dinero?, GobiernoUSA.gov
• Osamu Corporation Voluntarily Recalls Frozen Tuna Products from Distributors Due To Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Osamu Corporation Voluntarily Recalls Frozen Yellow Fin Tuna Chunk Meat Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• ¿Necesita saber cómo abrir una cuenta bancaria o transferir dinero?, GobiernoUSA.gov
• Update of CVM's What's New - The Natural Dog Company, Inc. Recalls 12" Tremenda Sticks Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• The Natural Dog Company, Inc. Recalls 12" Tremenda Sticks Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Veterinary Feed Directive Brochures Available, U.S. Food & Drug Administration (FDA)
• Updated Press Release - It Takes A Village Foods LLC. Dba Veggie Evolution Issues An Allergy Alert On Undeclared Soy In Veggie Evolution Kale Crisps Zen Nori, U.S. Food & Drug Administration (FDA)
• Barrel O' Fun Snack Foods Co. Issues Allergy Alert On Undeclared Milk In Vic's Original Popcorn (1-1/8oz), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - 0.9 Percent Sodium Chloride Injection, USP, 50mL and 100mL by Baxter: Recall - Particulate Matter, FDA MedWatch
• Baxter Initiates Voluntary Recall Of Two Lots Of IV Solutions Due To The Potential Presence Of Particulate Matter, U.S. Food & Drug Administration (FDA)
• It Takes A Village Foods Llc. Dba Veggie Evolution Issues An Allergy Alert On Undeclared Soy In Veggie Evolution Kale Crisps Zen Nori, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - New Food Related Emergency Exercise, U.S. Food & Drug Administration (FDA)
• SUPERVALU ISSUES ALLERGY ALERT ON UNDECLARED MILK IN CUB FOODS AND RAINBOW FOODS DANISH ROLLS 4CT., U.S. Food & Drug Administration (FDA)
• Apele una decisión del Seguro Social por Internet, GobiernoUSA.gov
• FDA MedWatch - Proglycem (diazoxide): Drug Safety Communication - Reports of Pulmonary Hypertension in Infants and Newborns, FDA MedWatch
• FDA authorizes use of prosthesis for rehabilitation of above-the-knee amputations, U.S. Food & Drug Administration (FDA)
• D&D Foods Issues Allergy Alert on Undeclared Milk and Wheat in Hy-Vee American Macaroni Salad, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 15, 2015, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Medtronic Shiley Neonatal and Pediatric Tracheostomy Tubes: Switching Tubes May Cause Breathing Issues, U.S. Food & Drug Administration (FDA)
• Estafas de inmigración relacionadas con los notarios públicos, GobiernoUSA.gov
• Mylan Institutional LLC, U.S. Food & Drug Administration (FDA)
• >Homemade recalls Pickles and Sauces because of possible health risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Calcium Chloride Intravenous Infusion 10% w/v 10mL Prefilled Syringe by Mylan: Market Withdrawal - Difficulties in Administration, FDA MedWatch
• Seguridad en la playa: cómo evitar ser atacado por un tiburón, GobiernoUSA.gov
• What to Do If You Think You’ve Purchased a Recalled Food, FoodSafety.gov
• FDA MedWatch - June 2015 Safety Labeling Changes includes 30 products with revisions to Prescribing Information, FDA MedWatch
• CFSAN Constituent Update - FDA to Hold Public Meeting in Preparation for International Cooperation on Cosmetics Regulation (ICCR) Meeting, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA takes steps to prevent sales of unapproved kidney drugs for dogs and cats, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Carnivore Meat Company, LLC Voluntarily Issues a Recall Two Batches of Raw Pet Treats, U.S. Food & Drug Administration (FDA)
• Nectar Foods, Inc. Issues Allergy Alert on Undeclared Almond in CocoNoNut Cacao-Nectar Bar, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lariat Suture Delivery Device for Left Atrial Appendage (LAA) Closure by SentreHEART: FDA Safety Communication - Reports of Patient Deaths and Other Serious Adverse Events, FDA MedWatch
• FDA approves new drug to treat schizophrenia and as an add on to an antidepressant to treat major depressive disorder, U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Use of LARIAT Suture Delivery Device for Left Atrial Appendage Closure: FDA Safety Communication, U.S. Food & Drug Administration (FDA)
• Stella & Chewy's Voluntarily Recalls Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• The July 2015 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Carnivore Meat Company, LLC Voluntarily Issues a Recall Two Batches of Raw Pet Treats, U.S. Food & Drug Administration (FDA)
• Maya Overseas Foods Inc. Recalls Cashew Split Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 08, 2015, U.S. Food & Drug Administration (FDA)
• Averigüe si el Gobierno le debe dinero, GobiernoUSA.gov
• FDA MedWatch - Non-aspirin Nonsteroidal Anti-inflammatory Drugs (NSAIDs): Drug Safety Communication - FDA Strengthens Warning of Increased Chance of Heart Attack or Stroke, FDA MedWatch
• CFSAN Constituent Update - Menu Labeling Compliance Date, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • CFSAN Constituent Update - Menu Labeling Compliance Date, U.S. Food & Drug Administration (FDA)
• Los resultados de la lotería de visas (2014 y 2015) ya están disponibles, GobiernoUSA.gov
• Arthur Schuman issues Allergy Alert on Undeclared Egg in Grated Parmesan Cheese, U.S. Food & Drug Administration (FDA)
• What do Millennials and the USDA Meat and Poultry Hotline Have in Common? – The Big 3-0, FoodSafety.gov
• Brett Anthony Foods Issues Recall For Undeclared Milk In Whole Foods Market Branded Vegetable Chili Sold From Whole Foods Market Naperville, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Stella & Chewy’s Voluntarily Recalls Products Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for July 01, 2015, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listings of Approved Medicated Feed Mill Licenses and Veterinary Feed Directive Distributor Notifications, U.S. Food & Drug Administration (FDA)
• Whole Foods Market's Southwest Region Recalls Cherry, Blackberry and Peach Pies in Four Stores Due to Undeclared Egg, U.S. Food & Drug Administration (FDA)
• Boulder Dog Food Company, L.L.C. Voluntarily Recalls Seven Bags of Turkey Sprinkles, 3 oz with A “Best By” Date of “05/18/16, 05/28/2016 and 05/30/2016” Due to Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Celebre este 4 de Julio aprendiendo más sobre la historia de EE. UU., GobiernoUSA.gov
• Test Please do not reply, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lifesaver Single Patient Use Manual Resuscitator by Teleflex Hudson RCI: Class I Recall - Intake Port Blockage, FDA MedWatch
• Update of CVM's What's New - Animal Drug Approvals July 2015 Update (Green Book), U.S. Food & Drug Administration (FDA)
• Medical Device Safety and Recalls: Teleflex Hudson RCI Lifesaver Single Patient Use Manual Resuscitator Intake Port Blockage, U.S. Food & Drug Administration (FDA)
• CFSAN Constituent Update - Supplement to the 2013 Food Code, U.S. Food & Drug Administration (FDA)
• Natural Grocers® issues recall on 10oz. Caribbean Nut & Fruit Mix due to possible health risk, U.S. Food & Drug Administration (FDA)
• Orgulloso de ser ciudadano americano, GobiernoUSA.gov
• FDA MedWatch - FLOW-i Anesthesia Systems by Maquet: Class 1 Recall - Dislodged Patient Cassette May Stop Patient Ventilation, FDA MedWatch
• Medical Device Safety and Recalls: FLOW-i Anesthesia Systems - Dislodged Patient Cassette May Stop Patient Ventilation, U.S. Food & Drug Administration (FDA)
• FDA Drug Safety Communication: Using codeine cough-and-cold medicines in children, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Unapproved Prescription Ear Drop (Otic) Products: Not FDA Evaluated for Safety, Effectiveness and Quality, FDA MedWatch
• FDA MedWatch - Codeine Cough-and-Cold Medicines in Children: Drug Safety Communication - FDA Evaluating Potential Risk of Serious Side Effects, FDA MedWatch
• Show Us When You Are #GrillingLikeaPRO, FoodSafety.gov
• Kaletra (lopinavir/ritonavir) product labeling was updated, U.S. Food & Drug Administration (FDA)
• Rocky Mountain Foods, Inc. Voluntarily Recalls Free Range Snack Co. Brand 16 oz. Island Fruit and Nut Trail Mix and Bulk Macadamia Nuts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)