FDA News

• Thread Index

• Beta Labs, LTD Announces a Recall of Dietary Supplements Oxyphen, Phentalene, Phen FX, and Red Vipers Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Vibativ for hospitalized patients with bacterial pneumonia
  • From: U.S. Food & Drug Administration (FDA)
• Taylor Farms New Jersey Issues Allergy Alert on Undeclared Tree Nuts in Black Forest Ham and Cheese on a Pretzel Roll with Swiss Cheese and Country Dijon Honey Mustard
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medtronic Xomed NIM Trivantage EMG Endotracheal Tube: Class I Recall - Cuff Leak or Cuff Deflation When Inflation Valve Cap Inappropriately Removed
  • From: FDA MedWatch
• CVM Updates - FDA Announces Grant Funding Available for Veterinary Testing Methods
  • From: U.S. Food & Drug Administration (FDA)
• DOJ News Release: The Department of Justice Files Suit Against Louisiana Pharmaceutical Company for Distributing Unapproved and Misbranded Prescription and Over-the-counter Drugs
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Plan B One-Step emergency contraceptive for use without a prescription for all women of child-bearing potential
  • From: U.S. Food & Drug Administration (FDA)
• FDA obtains waiver from European Commission to facilitate export for U.S. pharmaceutical manufacturers
  • From: U.S. Food & Drug Administration (FDA)
• Granna's LLC Voluntarily Recalls Packages of #705 Tuna Mac With Italian Blend Vegetables and Spiced Apple Rings Due to Undeclared Eggs
  • From: U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update -
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Respironics California, Inc. - Class 1 Recall: V60 Ventilators - Issue with software
  • From: FDA MedWatch
• FDA approves first genotyping test for patients with hepatitis C virus
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Public Meeting on Expanded Drug Supply Chain Authorities
  • From: U.S. Food & Drug Administration (FDA)
• Garden-Fresh Foods, Inc. Voluntarily Recalls Limited Packages of Archer Farms Smoked Salmon Dip Because of Possible Mislabeling
  • From: U.S. Food & Drug Administration (FDA)
• Advance Pharmaceutical Inc. Issues Voluntary Recall of One Lot of Enteric Coated Aspirin Tablets, 81 mg, Due to Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 19, 2013
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Enteric Coated Aspirin 81 mg Tablets by Advance Pharmaceutical Inc.: Recall of One Lot - May Contain Acetaminophen 500 mg tablets
  • From: FDA MedWatch
• Update of CVM's What's New
  • From: U.S. Food & Drug Administration (FDA)
• Oskri is Expanding the Recall of Fig Dark Chocolate Bars to Include Additional Lots. Lot: 161 through 164
  • From: U.S. Food & Drug Administration (FDA)
• Nuevo servicio informativo de USCIS en Español
  • From: GobiernoUSA.gov
• Natura Pet Issues Voluntary Recall of Specialized Dry Pet Foods Due to a Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Zyprexa Relprevv (Olanzapine Pamoate): Drug Safety Communication - FDA Investigating Two Deaths Following Injection
  • From: FDA MedWatch
• FDA MedWatch - Endologix, Inc. AFX Introducer System: Class 1 Recall - Reports Of Dilator Breaking During Procedures
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Cybersecurity for Medical Devices and Hospital Networks: FDA Safety Communication
  • From: FDA MedWatch
• CVM Updates - FDA Announces the Reauthorization of User Fees to Support Timely and Efficient Review of Animal Drugs and Generic Animal Drugs
  • From: U.S. Food & Drug Administration (FDA)
• Oskri Recalls “Coconut Bar Dark Chocolate”, “Coconut Bar Dark Chocolate Minis”, “Fig Dark Chocolate Bars” and “Almond Dark Chocolate Bars” Because of Undeclared Milk
  • From: U.S. Food & Drug Administration (FDA)
• See’s Candies, Inc. Issues Allergy Alert on Undeclared Nuts and Eggs in Milk and Dark Raisins
  • From: U.S. Food & Drug Administration (FDA)
• Consejos para fortalecer la relación padre-hijo
  • From: GobiernoUSA.gov
• Lipari Foods Recalls Sunflower Seeds and Snack Mixes Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Vega Issues Allergy Alert on Undeclared Milk in Vega One Bars and Vega Sport Protein Bars
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - May 2013 Safety Labeling Changes includes 40 products with revisions to Prescribing Information
  • From: FDA MedWatch
• Butterfly Bakery Issues Allergy Alert of Undeclared Walnuts
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Xgeva to treat giant cell tumor of the bone
  • From: U.S. Food & Drug Administration (FDA)
• Sagent Pharmaceuticals Expands a Nationwide Voluntary Recall to All Lots of Vecuronium Bromide for Injection, 10mg Single Use Vials Manufactured by Mustafa Nevzat (MN Pharmaceuticals)
  • From: U.S. Food & Drug Administration (FDA)
• Salud de los hombres
  • From: GobiernoUSA.gov
• Update of CVM's What's New - Hartz Mountain Corporation is Voluntarily Recalling One Specific Lot of 1.2 oz. Size of Wardley Betta Fish Food Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Kid's Page Article
  • From: U.S. Food & Drug Administration (FDA)
• Hartz Mountain Corporation is Voluntarily Recalling One Specific Lot of 1.2 oz. Size of Wardley Betta Fish Food Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Verifique las cuentas de redes sociales del Gobierno
  • From: GobiernoUSA.gov
• Zydus Pharmaceuticals USA Inc. Issues Voluntary Nationwide Recall of Warfarin 2 mg Tablets, Lot MM5767, Expiration Date June 2014, Due to Oversized Tablets
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 12, 2013
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Warfarin 2 mg Tablets by Zydus Pharmaceuticals USA Inc.: Recall - Due to Oversized Tablets
  • From: FDA MedWatch
• FDA MedWatch - Symbios GOPump and GOBlock Kits: Class 1 Recall - Potential for Excessive High Flow Rates
  • From: FDA MedWatch
• Julian’s Recipe Issues Voluntary Withdrawal of European Style Pretzel Baguette Boxes at Heb Stores in Texas
  • From: U.S. Food & Drug Administration (FDA)
• Bethel Nutritional Consulting, Inc. Issues a Voluntary Recall of Weight Loss Pills “Bethel 30” Found to Contain an Undeclared Drug Ingredient
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vecuronium Bromide For Injection by Sagent Pharmaceuticals, Inc.: Recall - Elevated Impurity Result Detected
  • From: FDA MedWatch
• HIV/AIDS Update - New new FDA Guidance for Industry: Developing Antiretroviral Drugs for Treatment
  • From: U.S. Food & Drug Administration (FDA)
• Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of Three Lots of Vecuronium Bromide for Injection, 10mg Manufactured by Mustafa Nevzat (MN Pharmaceuticals) Due to Elevated Impurity Levels
  • From: U.S. Food & Drug Administration (FDA)
• Al nadar ponga en práctica medidas de seguridad
  • From: GobiernoUSA.gov
• Alderman Farms Sales Corporation Voluntarily Recalls Organic Cherry Tomatoes Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• The June 2013 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Main Street Family Pharmacy in Tennessee: UPDATE - FDA has identified bacterial and fungal growth in samples of preservative-free (PF) methylprednisolone acetate
  • From: FDA MedWatch
• Update of CVM's What's New - Presentations Available from FDA's Data Quality Webinar Related to 2008 ADUFA Reauthorization
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for June 05, 2013
  • From: U.S. Food & Drug Administration (FDA)
• UPDATED RELEASE #2 Harris Teeter Lot Code and Best By Correction Townsend Farms Voluntarily Recalls Limited Lots of Frozen Organic Antioxidant Blend Products Due To Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Creole and Company, LLC Issues Allergy Alert on Undeclared Milk, Soy, and Wheat in Creole Bisque
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - 2013 AAVPT/CVM Animal Drugs in Feeds Workshop
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• General Mills Voluntarily Recalls Single-Serve Reduced-Sugar Cinnamon Toast Crunch Bowlpak sold in Foodservice Establishments
  • From: U.S. Food & Drug Administration (FDA)
• Prime Food USA Issues an Alert On Listeria In Latis Brand Seafood Products
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - HIV Patient-Focused Drug Development Meeting: Backgrounder Document
  • From: U.S. Food & Drug Administration (FDA)
• Gromex Inc. Issues Allergy Alert on Undeclared Sulfites in Camaron Entero (Dried Whole Shrimp)
  • From: U.S. Food & Drug Administration (FDA)
• Townsend Farms Voluntarily Recalls Limited Lots of Frozen Organic Antioxidant Blend Products Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals June 2013 Update (Green Book)
  • From: U.S. Food & Drug Administration (FDA)
• Food Co. Recalls Gouda Cheeses Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Nephron Pharmaceuticals Corp. EZ Breathe Atomizer: Class 1 Recall - Washer Could Become Dislodged
  • From: FDA MedWatch
• FDA MedWatch Celebrates 20 Years and Announces the Availability of New Consumer-Friendly Reporting Form and MedWatchLearn Tool
  • From: FDA MedWatch
• Investigan nuevo brote de Hepatitis A
  • From: GobiernoUSA.gov
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listings of Veterinary Feed Directive Distributor Notifications and Approved Medicated Feed Mill Licenses
  • From: U.S. Food & Drug Administration (FDA)
• Blessing Inc. Issues Voluntary Recall On 16-20 Domestic EZ Peel Shrimp
  • From: U.S. Food & Drug Administration (FDA)
• UPDATE-Salmolux Voluntarily Recalls Cold Smoked Salmon Products Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• International Desserts ISSUES ALLERGY ALERT ON UNDECLARED Walnuts IN Uncle Eddies Vegan Oatmeal Chocolate Cookies
  • From: U.S. Food & Drug Administration (FDA)
• 5 actividades para disfrutar el verano en familia
  • From: GobiernoUSA.gov
• Update of CVM's What's New: 2013 Advisory Action letter
  • From: U.S. Food & Drug Administration (FDA)
• A new HealthCare.gov--plus the latest info about your state
  • From: Health Insurance Marketplace
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Cheryl's Issues A Voluntary Nationwide Recall On Its 1.6 oz. Buttercream Frosted Cinnamon Pumpkin Cookies Due To Undlecared Peanuts
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 29, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Educación para niños con discapacidades, en GobiernoUSA.gov
  • From: GobiernoUSA.gov
• FDA MedWatch - Olympia Pharmacy Sterile Compounded Products: Recall - Concerns About Sterility Assurance
  • From: FDA MedWatch
• FDA MedWatch - Magnesium Sulfate: Drug Safety Communication - Recommendation Against Prolonged Use in Pre-term Labor
  • From: FDA MedWatch
• Lowlite Investments, Inc. d/b/a Olympia Pharmacy Announces a Voluntary Multi-State Recall of All Sterile Compounded Products Compounded Between December 17, 2012, and March 27, 2013, Due to Concerns About Sterility Assurance
  • From: U.S. Food & Drug Administration (FDA)
• Limited Number Of Lightlife Farmer’s Market Veggie Burgers Recalled Due To Undeclared Milk Allergen
  • From: U.S. Food & Drug Administration (FDA)
• Ebproduce SA de RL Recalls Fresh Thai Peppers Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves two drugs, companion diagnostic test for advanced skin cancer
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Information on How to Participate in the Data Quality Webinar Related to 2008 ADUFA Reauthorization is Now Available
  • From: U.S. Food & Drug Administration (FDA)
• Win Luck Trading Inc. Issues Allergy Alert on Undeclared Eggs in Lam Sheng Kee's Shrimp Balls, Lobster Balls and Fish Package Eggs and Fresh Fish Cakes
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Magnesium Sulfate Injection by Fresenius Kabi USA: Recall - Glass Particles in Vials
  • From: FDA MedWatch
• Fresenius Kabi USA Initiates Voluntary Recall of Single Lot of Magnesium Sulfate
  • From: U.S. Food & Drug Administration (FDA)
• FDA announces import of injectable nutrition drugs
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Main Street Family Pharmacy, LLC Issues Voluntary Nationwide Recall of All Sterile Compounded Products
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Main Street Family Pharmacy in Tennessee: FDA Alerts Health Care Providers of Adverse Reactions Associated with Steroid Injections - Update
  • From: FDA MedWatch
• Salmolux Recalls Cold Smoked Salmon Products Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Eco-Cuisine Recalls Product Because of Possible Health Risk (Extended Recall)
  • From: U.S. Food & Drug Administration (FDA)
• A por un verano divertido, seguro y saludable
  • From: GobiernoUSA.gov
• FDA MedWatch - Main Street Family Pharmacy in Tennessee: FDA Alerts Health Care Providers of Adverse Reactions Associated with Steroid Injections
  • From: FDA MedWatch
• FDA alerts health care providers of adverse reactions associated with steroid injections from Main Street Family Pharmacy in Tennessee
  • From: U.S. Food & Drug Administration (FDA)
• Día de la Recordación - 27 de mayo
  • From: GobiernoUSA.gov
• FDA MedWatch - Cook Medical, Inc. Zilver PTX Drug-Eluting Peripheral Stent: Class 1 Recall - Complaints of Delivery System Tip Separation
  • From: FDA MedWatch
• Cuide de la salud de sus ojos
  • From: GobiernoUSA.gov
• FDA allows marketing of first A1c test labeled for diagnosing diabetes
  • From: U.S. Food & Drug Administration (FDA)
• Order a FREE Friends and Family Health Kit today!
  • From: FDA Office of Women's Health
• Manejo del estrés después de un evento traumático
  • From: GobiernoUSA.gov
• Enforcement Report for May 22, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Letter to Bovine Veterinarians – GONAbreed
  • From: U.S. Food & Drug Administration (FDA)
• Tornados en Oklahoma: Solictud de asistencia y cómo ayudar
  • From: GobiernoUSA.gov
• LL Bakery, Inc. Announces the Recall of White Farm Enriched White Bread, Butter Farm Enriched White Bread, and Italian Cream Danish for Undeclared Milk Allergens
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Methotrexate Sodium, USP Injectable Vials by Sandoz US: Recall - Particulate Matter In Vials
  • From: FDA MedWatch
• Eco-Cuisine Recalls Product Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Sandoz US Announces Voluntary Nationwide Recall of two lots of Methotrexate Sodium, USP, Injectable Vials, 25mg/mL, 40mL vials
  • From: U.S. Food & Drug Administration (FDA)
• Precautionary Recall Issued For Pre-Packaged Texas Gulf Shrimp
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Abbott Diabetes Care: Class 1 Recall - FreeStyle InsuLinx Blood Glucose Meters - Risk of Incorrect Test Result
  • From: FDA MedWatch
• Atención: Estafadores engañan sobre el nuevo mercado de seguros médicos
  • From: GobiernoUSA.gov
• HIV/AIDS Update - Tentative approval of lamivudine and tenofovir disoproxil fumarate Tablets, 300 mg/300 mg
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - All Sterile Drug Products Made and Distributed By NuVision Pharmacy Dallas Facility: Recall - Lack Of Sterility Assurance
  • From: FDA MedWatch
• FDA MedWatch - Compounded Prescription Therapies By Pentec Health Inc.: Recall - Lack Of Sterility Assurance
  • From: FDA MedWatch
• Pentec Health Announces Limited Voluntary Recall of Certain Compounded Prescription Therapies for Renal Patients
  • From: U.S. Food & Drug Administration (FDA)
• FDA seeks preliminary injunction against New York fish manufacturer
  • From: U.S. Food & Drug Administration (FDA)
• Tropical Valley Foods Issues Allergy Alert on Undeclared Milk and Walnuts in Next by Nature Dark Chocolate Bananas
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Rural King Recalls Deer Corn Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Rural King Recalls Deer Corn Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Symbios Medical Products Issues Nationwide Recall of GOPump and GOBlock Kits
  • From: U.S. Food & Drug Administration (FDA)
• Cómo prepararse para los nuevos mercados de seguros médicos
  • From: GobiernoUSA.gov
• Update of CVM's What's New - Current Animal Food GRAS Notices Inventory
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 15, 2013
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch -
  • From: FDA MedWatch
• FDA approves new drug for advanced prostate cancer
  • From: U.S. Food & Drug Administration (FDA)
• Salud de las mujeres
  • From: GobiernoUSA.gov
• HIV/AIDS Update - Public Meeting on HIV Patient-Focused Drug Development and HIV Cure Research: June 14, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Spring eUpdate: Pregnancy Medication Safety, Mammography Myths & More
  • From: FDA Office of Women's Health
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Beamonstar Products Issues Voluntary Nationwide Recall of SexVoltz, Velextra, & Amerect Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients- Expanded to Include SexVoltz 12 Capsules Bottle, SKU 626570615316.
  • From: U.S. Food & Drug Administration (FDA)
• Additional Lots Added: Voluntary Nationwide Recall of 21 Lots of Piperacillin and Tazobactam for Injection, USP 40.5 Grams Due to Possibility of Precipitation / Crystallization in IV Bag or IV Line Upon Reconstitution
  • From: U.S. Food & Drug Administration (FDA)
• In Cooperation with FDA, The Compounding Shop, LLC Declares a Voluntary Recall of All Lots of Sterile Compounded Products Due to a Lack of Sterility Assurance Distributed Within its Local Market Area
  • From: U.S. Food & Drug Administration (FDA)
• Hannaford Supermarkets Issues Allergy Alert for Two Bakery Cookie Products That May Contain Undeclared Nuts
  • From: U.S. Food & Drug Administration (FDA)
• Smart & Final Expands Recall to Include Additional Production Dates; Allergy Alert - Undeclared Wheat, Milk and Eggs in La Romanella Tri-Color Cheese Tortellini
  • From: U.S. Food & Drug Administration (FDA)
• The May 2013 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Breo Ellipta to treat chronic obstructive pulmonary disease
  • From: U.S. Food & Drug Administration (FDA)
• Krinos Foods, LLC. is Expanding its April 28, 2013 Recall to Include Additional Expiration Dates Jan 01-2014 to Jun 01-2014 of Tahini Products Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Dairy Fresh Conducts Voluntary Recall of IGA Brand “Vanilla & Chocolate” 1.75 Quart Ice Cream Because Package May Contain Undeclared Allergens (Almonds, Coconut, Soy)
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Bimeda-MTC Animal Health Inc. Issues Voluntary Nationwide Recall of Sterile Solutions Due to Concerns Regarding Sterility and Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Pure Herbs Ltd. Issues Allergy Recall Alert on Undeclared Allergens (Milk and Soy) in Protein Extract Urgent Undeclared Allergen Labeling Recall In Pure Herbs Ltd. Protein Extract
  • From: U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recalls Mislabeled Curried Chicken Salad and Vegan Chick’n Salad Sold at the Cold Salad Bar Due to Undeclared Allergens
  • From: U.S. Food & Drug Administration (FDA)
• Bimeda Inc. on Behalf of Manufacturer Bimeda-MTC Animal Health Inc. Issues Voluntary Nationwide Recall of Sterile Solutions Due to Concerns Regarding Sterility and Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Atriphen dietary supplement (Xymogen brand): Recall - Potential Allergic Reaction Due to Milk and Soy
  • From: FDA MedWatch
• XYMOGEN identifies allergen oversight by third-party manufacturer; issues recall of artriphen™
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 08, 2013
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - The Compounding Shop: FDA News Release - Lack of Sterility Assurance of Drug Products
  • From: FDA MedWatch
• Beneficio Adicional de Medicare
  • From: GobiernoUSA.gov
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Beamonstar Products Issues Voluntary Nationwide Recall of SexVoltz, Velextra, & Amerect Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients
  • From: U.S. Food & Drug Administration (FDA)
• USCIS responde a sus preguntas sobre inmigración
  • From: GobiernoUSA.gov
• FDA MedWatch -
  • From: FDA MedWatch
• FDA MedWatch - Medtronic: Class 1 Recall - Medtronic Deep Brain Stimulation Lead Kit and Activa Dystonia HDE Kit
  • From: FDA MedWatch
• Disfrute del sabor de la primavera
  • From: GobiernoUSA.gov
• FDA MedWatch - Covidien Surgical Stapler Reloads: FDA Safety Communication - Devices Stolen Before They Were Sterilized
  • From: FDA MedWatch
• FDA MedWatch - Cardinal Health: Class 1 Recall - Various Presource Kits Containing a Pre-Assembled Anesthesia Circuit
  • From: FDA MedWatch
• Update of CVM's What's New - Cargill’s Animal Nutrition Business Conducts Voluntary Recall of Lamb Feed
  • From: U.S. Food & Drug Administration (FDA)
• Cargill’s Animal Nutrition Business Conducts Voluntary Recall of Lamb Feed
  • From: U.S. Food & Drug Administration (FDA)
• FDA warns pregnant women to not use certain migraine prevention medicines
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Valproate Anti-Seizure Products: Drug Safety Communication - Contraindicated for Pregnant Women for Prevention of Migraine Headaches
  • From: FDA MedWatch
• FDA MedWatch - Kadcyla (ado-trastuzumab emtansine): Drug Safety Communication - Potential Medication Errors Resulting from Name Confusion
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• ¿Tiene preguntas sobre temas de inmigración?
  • From: GobiernoUSA.gov
• HIV/AIDS Update - Sustiva (efavirenz) pediatric patients labeling update
  • From: U.S. Food & Drug Administration (FDA)
• Medtronic Announces FDA Classification Of Deep Brain Stimulation Lead Cap Communication
  • From: U.S. Food & Drug Administration (FDA)
• Nestle USA Announces Voluntary Recall of Select Varieties/Production Codes of California Pizza Kitchen and DiGiorno Frozen Pizzas
  • From: U.S. Food & Drug Administration (FDA)
• American Lifestyle Issues a Worldwide Voluntary Recall of Vicerex Capsules and Black Ant Capsules, Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Veterinary Master Files
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals May 2013 Update (Green Book)
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Cancellation of 2013 Windows to Regulatory Research Internship Program
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for May 01, 2013
  • From: U.S. Food & Drug Administration (FDA)
• ¿Qué es la discriminación en el trabajo?
  • From: GobiernoUSA.gov
• FDA MedWatch - Newport Medical Instruments, Inc., HT70 and HT70 Plus Ventilators: Class I Recall - Unit Goes Into Internal Backup Battery Sooner Than Expected
  • From: FDA MedWatch
• Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports
  • From: U.S. Food & Drug Administration (FDA)
• FDA Veterinarian - May 1, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Krinos Foods, LLC. Voluntarily Recalls Tahini Jars Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Prime Food USA Issues an Alert on Listeria in Latis Brand Herring Fillet "Antalja" in Oil and Latis Brand Herring Fillet in Oil with Spices
  • From: U.S. Food & Drug Administration (FDA)
• Carson’s Deli & Bakery Issues Allergy Alert For Undeclared Allergens In Assorted Cookie Pack And Fudge Brownie Cookie
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Anticoagulant Citrate Phosphate Dextrose Solution, USP (CPD) BLOOD-PACK Unit By Fenwal: Recall - Labeling Issue Identified
  • From: FDA MedWatch
• FDA approves Plan B One-Step emergency contraceptive without a prescription for women 15 years of age and older
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
  • From: U.S. Food & Drug Administration (FDA)
• Done vida: inscríbase en su estado
  • From: GobiernoUSA.gov
• FDA MedWatch - Samsca (Tolvaptan): Drug Safety Communication - FDA Limits Duration and Usage Due To Possible Liver Injury Leading to Organ Transplant or Death
  • From: FDA MedWatch
• FDA MedWatch - Piperacillin and Tazobactam for Injection, USP 40.5 grams: Recall - Precipitation or Crystallization in IV Bag or IV Line Upon Reconstitution
  • From: FDA MedWatch
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listing of Medicated Feed Mill Licenses/Veterinary Feed Directive Distributors
  • From: U.S. Food & Drug Administration (FDA)
• Sirven comidas nutritivas durante el verano a niños que las necesitan
  • From: GobiernoUSA.gov
• Voluntary Nationwide Recall of 15 Lots of Piperacillin and Tazobactam for Injection, USP 40.5 Grams Due to Possibility of Precipitation / Crystallization in IV Bag or IV Line Upon Reconstitution
  • From: U.S. Food & Drug Administration (FDA)
• Smart & Final issues Recall - Allergy Alert Undeclared Wheat, Milk and Eggs in La Romanella Tri-Color Cheese Tortellini
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Kcentra for the urgent reversal of anticoagulation in adults with major bleeding
  • From: U.S. Food & Drug Administration (FDA)
• Proteja a su bebé de infecciones
  • From: GobiernoUSA.gov
• Maple View Farm Recalls Three Flavors of Ice Cream Because of Undeclared Allergens
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hospira Inc., GemStar Infusion System: Recall - Lithium Battery Low Voltage
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Hospira Issues a Voluntary Nationwide Recall of One Lot Of 0.9% Sodium Chloride Injection, Usp, 100 Ml, Flexible Containers Due to Particulate – Revised to Update Stericycle Phone Number
  • From: U.S. Food & Drug Administration (FDA)
• Orville Redenbacher’s® Classic Kettle Korn Ready-to-eat Popcorn Recalled Due to Undeclared Milk Allergen
  • From: U.S. Food & Drug Administration (FDA)
• Únase a la charla sobre salud de las minorías
  • From: GobiernoUSA.gov
• FDA MedWatch - Potiga (Ezogabine): Drug Safety Communication - Linked To Retinal Abnormalities And Blue Skin Discoloration
  • From: FDA MedWatch
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Eba Multivitamin Supplement By Saratoga Therapeutics LLC: Recall - Allergy Alert On Undeclared Milk Components
  • From: FDA MedWatch
• Saratoga Therapeutics, LLC Issues Allergy Alert on Undeclared Milk Components in Eba Multivitamin Supplement
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sodium Chloride Injection 0.9 percent USP, 100 mL Flexible Containers by Hospira: Recall - Particulate Matter
  • From: FDA MedWatch
• Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection, USP, 100 ML, Flexible Containers Due to Particulate
  • From: U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Changes to label for Atripla (efavirenz/emtricitabine/tenofovir disoproxil fumarate) tablets
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
  • From: U.S. Food & Drug Administration (FDA)
• Potential for Delivery System Catheter Separation Prompts Cook Medical to Initiate Voluntary Global Recall of Zilver® PTX® Drug Eluting Stent
  • From: U.S. Food & Drug Administration (FDA)
• Prevenga el maltrato infantil
  • From: GobiernoUSA.gov
• HIV/AIDS Update- Prezista (darunavir) labeling changes
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 24, 2013
  • From: U.S. Food & Drug Administration (FDA)
• ¡Cuidado con el "desafío de la canela"!
  • From: GobiernoUSA.gov
• 7th Heaven Bakeries Issues Allergy Alert on Undeclared Egg, Soy And Milk in Oatmeal Raisin Cookies
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GE Healthcare, Giraffe OmniBed and Giraffe Incubator: Class I Recall - Device May Randomly Delete Stored Information When Powered On
  • From: FDA MedWatch
• App IRS2Go, ahora en español
  • From: GobiernoUSA.gov
• FDA MedWatch - LifeScan, Inc.OneTouch Verio IQ Blood Glucose Meter - Recall: Failure to provide a warning at extremely high blood glucose levels
  • From: FDA MedWatch
• FDA MedWatch - All Sterile Compounded Products by Nora Apothecary And Alternative Therapies: Recall - Lack of Sterility Assurance
  • From: FDA MedWatch
• Nationwide Voluntary Field Correction Action Issued for GE Healthcare’s Giraffe Incubator and Giraffe OmniBed with Servo Oxygen Control System
  • From: U.S. Food & Drug Administration (FDA)
• Nora Apothecary & Alternative Therapies Announces a Voluntary Multi-State Recall of All Sterile Compounded Products Due to a Lack of Sterility Assurance
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - CareFusion Alaris PC Unit with Software V9.12: Class 1 Recall - Communication Error When Attached to EtCO2 or SpO2 Modules
  • From: FDA MedWatch
• Go Max Go Foods LLC Issues Voluntary Withdrawal of Snap!, Cleo's, Jokerz, Twilight, Buccaneer, Thumbs Up and Mahalo Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• ¿Tiene preguntas sobre hipertensión?
  • From: GobiernoUSA.gov
• Update of CVM's What's New - FDA Announces Data Quality Webinar Related to 2008 ADUFA Reauthorization
  • From: U.S. Food & Drug Administration (FDA)
• Día del Planeta Tierra
  • From: GobiernoUSA.gov
• FDA MedWatch - Balanced Solutions All Sterile Compounded Products: Recall - Lack of Sterility Assurance
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Cautions in Interpretation of Antimicrobial Resistance Data
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Natura Pet Expands Voluntary Recall of Dry Pet Foods Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Natura Pet Expands Voluntary Recall of Dry Pet Foods Due to Possible Health Risk.
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Merit Bird Company, LLS Recalls Vitae Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Merit Bird Company, LLS Recalls Vitae Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Medical Bed Mattresses: FDA Safety Communication - Damaged or Worn Covers Pose Risk of Contamination and Infection
  • From: FDA MedWatch
• Update of CVM's What's New - CVM Issues Two Field Assignment
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Covidien Issues Voluntary Recall of Power Pac Batteries for Newport™ HT70 and HT70 Plus Ventilators
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch -
  • From: FDA MedWatch
• Sus documentos vitales cuando los necesite
  • From: GobiernoUSA.gov
• Prime Food USA Issues an Alert On Listeria in Latis Brand Herring Fillet “Matiej”, Salmon Fillet Slices and Herring Fillet “Forelka” in Oil
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 17, 2013
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Changes to label for Atripla (efavirenz/emtricitabine/tenofovir disoproxil fumarate) tablets
  • From: U.S. Food & Drug Administration (FDA)
• Conozca más sobre el autismo
  • From: GobiernoUSA.gov
• Abbott Initiates Voluntary Recall of FreeStyle lnsulinx® Blood Glucose Meters in the United States
  • From: U.S. Food & Drug Administration (FDA)
• Cómo reportar información relacionada a las explosiones en Boston
  • From: GobiernoUSA.gov
• Wegmans Food Markets Announces Voluntary Recall of Select Wegmans Food You Feel Good About Roasted Red Pepper Dip, 8 oz., Due to Undeclared Milk and Eggs
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves abuse-deterrent labeling for reformulated OxyContin
  • From: U.S. Food & Drug Administration (FDA)
• Cedarlane Natural Foods, Inc. Issues Allergy Allert and Voluntary Recall on O Organics Black Bean Enchiladas 9 Oz Due to Mislabeling and Undeclared Allergens
  • From: U.S. Food & Drug Administration (FDA)
• Plantar un jardín es una buena actividad familiar
  • From: GobiernoUSA.gov
• Ayude a su hijo a llevar una vida más sana
  • From: GobiernoUSA.gov
• Winn-Dixie Issues Recall On Winn-Dixie Organic 100% Apple Juice
  • From: FoodSafety.gov
• FDA MedWatch - Sterile Products Compounded, Repackaged, and Distributed by ApothéCure: Recall - Sterility Assurance Concerns
  • From: FDA MedWatch
• FDA MedWatch - Lyophilized Products Compounded by NuVision Pharmacy: Recall - Sterility Assurance Concerns
  • From: FDA MedWatch
• CVM Updates - Court Suspends Approval of Enroflox 100 for Cattle
  • From: U.S. Food & Drug Administration (FDA)
• ApothéCure, Inc. Announces Voluntary Nationwide Recall of All Lots of All Sterile Products Compounded, Repackaged, and Distributed by ApothéCure, Inc. Due to Sterility Assurance Concerns
  • From: U.S. Food & Drug Administration (FDA)
• NuVision Pharmacy Announces Voluntary Nationwide Recall of All Lots of All Lyophilized Products Compounded by NuVision Pharmacy Due to Sterility Assurance Concerns
  • From: U.S. Food & Drug Administration (FDA)
• Winn-Dixie Issues Voluntary Recall On Winn-Dixie Organic 100% Apple Juice
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - March 2013 Safety Labeling Changes includes 53 products with revisions to Prescribing Information
  • From: FDA MedWatch
• Medicines in My Home Update: Safe Disposal of Fentanyl Transdermal System “Patches”
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Louisiana Firm Expands Recall of Cooked Meat, Poultry, and Deli Products Due To Listeria
  • From: FoodSafety.gov
• ALLERGY ALERT: Wild Blue Yonder Foods issues Recall due to Undeclared Almonds
  • From: FoodSafety.gov
• ¿Tiene preguntas sobre temas ambientales?
  • From: GobiernoUSA.gov
• Wild Blue Yonder Foods issues Recall-Allergy Alert- Undeclared Almonds in Chappaqua Crunch GF Simply Granola with Flax and Fruit
  • From: U.S. Food & Drug Administration (FDA)
• FDA Classifies Voluntary Shapematch® Cutting Guides Recall as Class I Recall
  • From: U.S. Food & Drug Administration (FDA)
• Green Valley Drugs Announces Voluntary Nationwide Recall of All Lots of All Sterile Products Compounded, Repackaged, and Distributed by Green Valley Drugs Due to Quality Control Concerns
  • From: U.S. Food & Drug Administration (FDA)
• Affirm XL, Inc Issues a Voluntary Nationwide Recall of Affirm XL Dietary Supplement Tablet, Lot 1190001 Due to Potential Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 10, 2013
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Green Valley Drugs: Recall of All Lots of All Sterile Products - Quality Control Concerns
  • From: FDA MedWatch
• Impuestos: sugerencias para el último minuto
  • From: GobiernoUSA.gov
• Medicines in My Home Update
  • From: U.S. Food & Drug Administration (FDA)
• Donar vida: una opción a considerar
  • From: GobiernoUSA.gov
• Update of CVM's What's New - FDA budget requests $4.7 billion to ensure safety of food supply and to modernize medical product safety
  • From: U.S. Food & Drug Administration (FDA)
• FDA budget requests $4.7 billion to ensure safety of food supply and to modernize medical product safety
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Helpful Information for Veterinarians – Antiparasitic Resistance in Cattle and Small Ruminants in the United States
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA Voice – Leave the Chocolate Out of Rover’s Celebrations
  • From: U.S. Food & Drug Administration (FDA)
• La trata de personas es una forma moderna de esclavitud
  • From: GobiernoUSA.gov
• Ley de Cuidado de Salud y su cobertura médica
  • From: GobiernoUSA.gov
• FDA MedWatch - BCI Remote Alarm Cables By Smith's Medical ASD, Inc.: Class 1 Recall - Cables Are Not Transferring Alarms
  • From: FDA MedWatch
• Ojo con las estafas tributarias más comunes
  • From: GobiernoUSA.gov
• Consumer Concepts Issues a Voluntary Nationwide Recall of ROCK-IT MAN All Natural Male Supplement Products Marketed as Dietary Supplements to Support Male Sexual Performance Due to Undeclared Active Ingredient
  • From: U.S. Food & Drug Administration (FDA)
• The April 2013 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Public Master Files (PMFs) in development updated
  • From: U.S. Food & Drug Administration (FDA)
• La adicción a las drogas o el alcohol es una enfermedad
  • From: GobiernoUSA.gov
• Update of CVM's What's New - Veterinary Oversight of Antimicrobial Use in Livestock; Public Meetings Agenda
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
  • From: U.S. Food & Drug Administration (FDA)
• Centerville Pie Company Issues Allergy Alert on Undeclared (Anchovies) Fish in Clam Pies
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Animas Corporation 2020 Insulin Infusion Pump: Class I Recall - False Alarm or Warning Sound
  • From: FDA MedWatch
• FDA MedWatch - BIVIGAM Immune Globulin Intravenous (Human), 10 Percent Liquid, 100 mL Sterile Vial: Recall - Visible Particles Observed
  • From: FDA MedWatch
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
  • From: U.S. Food & Drug Administration (FDA)
• Little Mermaid Smoke House Recalls Smoked Herring and Pickled Herring Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Se vence el plazo para pagar los impuestos
  • From: GobiernoUSA.gov
• Rich Products Corporation Expands Voluntary Recall to All Products Produced at Its Waycross, Georgia Facility Due to Possible Contamination with E. Coli O121
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Bravo! Issues a Voluntary Recall for Three Raw Frozen Food Diet for Dogs and Cats Because of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Bravo! Issues a Voluntary Recall for Three Raw Frozen Food Diet for Dogs and Cats Because of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for April 03, 2013
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval: efavirenz, emtricitabine and tenofovir Disoproxil fumarate tablets, 600 mg/200 mg/300 mg
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals April 2013 Update
  • From: U.S. Food & Drug Administration (FDA)
• ¿Ya presentó su declaración de impuestos?
  • From: GobiernoUSA.gov
• Cómo lidiar con las alergias de niños en primavera
  • From: GobiernoUSA.gov
• Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports
  • From: U.S. Food & Drug Administration (FDA)
• Pilot Projects Report Comment Period Extended until July 3, 2013
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sodium Chloride Injection, 0.9 percent, 1000 mL, Flexible Container: Recall - Brass Particulates
  • From: FDA MedWatch
• Update of CVM's What's New - Natura Pet Expands Voluntary Recall of Dry Pet Foods Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection Due to Brass Particulates
  • From: U.S. Food & Drug Administration (FDA)
• Natura Pet Expands Voluntary Recall of Dry Pet Foods Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Invokana to treat type 2 diabetes
  • From: U.S. Food & Drug Administration (FDA)
• Rich Products Corporation Announces a Voluntary Recall of Farm Rich® Mini Quesadillas, Farm Rich® Mini Pizza Slices, Farm Rich® Philly Cheese Steaks, Farm Rich® Mozzarella Bites, and Market Day® Mozzarella Bites Due to Possible Contamination with E. Coli O121
  • From: U.S. Food & Drug Administration (FDA)
• Lisy Corporation Issues Voluntary Recall on Undeclared Soy in 5 Seasoning Blends
  • From: U.S. Food & Drug Administration (FDA)
• Lifestyle Evolution Inc. (LEI), Issues Allergy Alert -- -Undeclared Milk in Lifestyle Evolution Inc.’s, NuGO FREE, NuGO Dark and NuGO Slim Non Dairy bars
  • From: U.S. Food & Drug Administration (FDA)
• Publix Issues Voluntary Recall on Publix Deli Tri Fruit and Grain Salad
  • From: U.S. Food & Drug Administration (FDA)
• Urgent-Heartland Gourmet, LLC issues Allergy Alert on Undeclared Milk in Gluten Free Baking Mixes
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
  • From: U.S. Food & Drug Administration (FDA)
• Food Product Recall by the Gift Shop at Buffalo Trace Distillery Due to Undeclared Allergens
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 27, 2013
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves new multiple sclerosis treatment: Tecfidera
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vascular Solutions Inc., Guardian II and Guardian II NC Hemostasis Valves: Class I Recall - Risk of Air Being Introduced Into Device
  • From: FDA MedWatch
• FDA MedWatch - Palimed Solutions, Inc. Sterile Compound Products: Recall - Visible Particulates Observed
  • From: FDA MedWatch
• La Preferida, Inc. Issues A Voluntary Recall Of La Spanish Version - Preferida Whole Pinto Beans 29 OZ. (Water & Salt)
  • From: U.S. Food & Drug Administration (FDA)
• Pallimed Solutions, Inc. Announces Voluntary Nationwide Recall of All Sterile Compounded Products Dispensed
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Spacelabs Anesthesia Workstations and Service Kits: Class 1 Recall - Defect in CAS I/II Absorbers
  • From: FDA MedWatch
• FDA approves TOBI Podhaler to treat a type of bacterial lung infection in cystic fibrosis patients
  • From: U.S. Food & Drug Administration (FDA)
• Affordable Care Act at 3: Looking Forward and Expanding Access
  • From: Health Insurance Marketplace
• Update of CVM's What's New - Jones Natural Chews Co Recalls Woofers Dog Treats Because Of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA issues proposal to improve the quality of automated external defibrillators
  • From: U.S. Food & Drug Administration (FDA)
• Servicios para personas con discapacidades, en GobiernoUSA.gov
  • From: GobiernoUSA.gov
• Affordable Care Act at 3: Increased Savings for Seniors
  • From: Health Insurance Marketplace
• FDA MedWatch - Clinical Specialties Compounding Pharmacy Products: Recall - All Sterile Products Recalled Due To Lack of Sterility Assurance
  • From: FDA MedWatch
• La Preferida, Inc. Issues A Voluntary Recall Of La Preferida Whole Pinto Beans 29 OZ. (Water & Salt)
  • From: U.S. Food & Drug Administration (FDA)
• New Chapter, Inc. Issues Voluntary Recall Undeclared soy identified in one lot of Probiotic Elderberry dietary supplement
  • From: U.S. Food & Drug Administration (FDA)
• Medprep Consulting Inc. Announces Voluntary Nationwide Recall Of All Lots Of All Compounded Products Due To Potential Mold Contamination -2
  • From: U.S. Food & Drug Administration (FDA)
• Clinical Specialties Compounding Pharmacy Announces Voluntary Nationwide Recall of All lots of Sterile Products Repackaged and Distributed by Clinical Specialties Compounding Due to Lack of Sterility Assurance
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 20, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Affordable Care Act at 3: Paying for Quality Saves Health Care Dollars
  • From: Health Insurance Marketplace
• FDA MedWatch - Avastin Unit Dose Syringes by Clinical Specialties: Recall - Potential For Serious Eye Infection
  • From: FDA MedWatch
• Daesang Issues Allergy Alert on Undeclared Peanuts in Mixed Soy Bean Paste (Sesame and Garlic)
  • From: U.S. Food & Drug Administration (FDA)
• Affordable Care Act at 3: Holding Insurance Companies Accountable
  • From: Health Insurance Marketplace
• Affordable Care Act at 3: Abby's Story
  • From: Health Insurance Marketplace
• Natura Pet Issues Voluntary Recall of Specialized Dry Pet Foods Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Natura Pet Issues Voluntary Recall of Specialized Dry Pet Foods Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers Not to Eat Certain ProtiDiet High Protein Chocolate Dream Bars Manufactured by Pro-Amino International, Inc., Quebec, Canada
  • From: U.S. Food & Drug Administration (FDA)
• Clinical Specialties Issues Voluntary Nationwide Recall of Avastin Unit Dose Syringes due to Potential Serious Eye Infection
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Symbios GOPump Elastomeric Infusion PumpKit: Class 1 Recall - Flow Restrictor Bead May Become Displaced from its Fitting
  • From: FDA MedWatch
• Affordable Care Act at 3: Consumer Protections
  • From: Health Insurance Marketplace
• CVM Updates - FDA Gives Tips to Prevent Salmonella Infection from Handling Feeder Rodents and Pet Reptiles and Amphibians
  • From: U.S. Food & Drug Administration (FDA)
• Medicines in My Home Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - An Overview of FDA's Public Meeting on Antiparasitic Drug Use and Resistance in Ruminants and Equines
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Med Prep Consulting Inc. Compounded Products: Recall - Potential Mold Contamination
  • From: FDA MedWatch
• Aumenta el robo de reembolsos de impuestos
  • From: GobiernoUSA.gov
• Vascular Solutions Zerusa Ltd. Issues Recall of Guardian II and Guardian II NC Hemostasis Valves
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Guidances Under Development for 2013
  • From: U.S. Food & Drug Administration (FDA)
• Vascular Solutions Zerusa Ltd. Issues Recall of Guardian II and Guardian II NC Hemostasis Valves
  • From: U.S. Food & Drug Administration (FDA)
• Nishimoto Trading Co., LTD Issues Allergy Alert on Undeclared Milk in Kameda Brand 4.37 oz Packages of Rice Cracker "Kotsubukko"
  • From: U.S. Food & Drug Administration (FDA)
• Grippo Foods Inc. Issues A Voluntary Recall Of All Sizes Of Their Plain Potato Chips, Bar-B-Q Potato Chips, Cheddar Cheese With A Touch Of Jalapeno Potato Chips, Hot Dill Pickle Potato Chips, Sweet Bermuda Onion Potato Chips And Salt & Vinegar Potato Chips Due To Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Medprep Consulting Inc. Announces Voluntary Nationwide Recall Of All Lots Of All Compounded Products Due To Potential Mold Contamination
  • From: U.S. Food & Drug Administration (FDA)
• Medprep Consulting Inc. Announces Voluntary Nationwide Recall Of All Lots Of Magnesium Sulfate 2gm In Dextrose 5 percent In Water, 50ml For Injecton Due To Mold Contamination
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Stryker Instruments Neptune 1 Silver and Neptune 2 Ultra Waste Management System (Neptune 1 Silver and Neptune 2 Ultra): Safety Communication - Reports of Serious Tissue Damage and Patient Death
  • From: FDA MedWatch
• Hágase la prueba de detección del VIH
  • From: GobiernoUSA.gov
• FDA MedWatch - Incretin Mimetic Drugs for Type 2 Diabetes: Early Communication - Reports of Possible Increased Risk of Pancreatitis and Pre-cancerous Findings of the Pancreas
  • From: FDA MedWatch
• ¿Conoce usted el sitio MedlinePlus en español?
  • From: GobiernoUSA.gov
• Update of CVM's What's New - Bravo! Recalls 2 lb Tubes of Chicken Blend-Raw Frozen Food Diet for Dogs and Cats (One Lot Code) Because of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Bravo! Recalls 2 lb Tubes of Chicken Blend-Raw Frozen Food Diet for Dogs and Cats (One Lot Code) Because of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 13, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Nueva app de alerta de tornados
  • From: GobiernoUSA.gov
• New Breast Cancer Product Approval and Upcoming Workshop
  • From: FDA Office of Women's Health
• FDA approves Lymphoseek to help locate lymph nodes in patients with certain cancers
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - February 2013 Safety Labeling Changes includes 35 products with revisions to Prescribing Information
  • From: FDA MedWatch
• FDA MedWatch - Azithromycin (Zithromax or Zmax): Drug Safety Communication - Risk of Potentially Fatal Heart Rhythms
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Green Planet, Inc. Issues a Voluntary Nationwide Recall of One Lot of "Night Bullet," a Product Marketed as a Dietary Supplement to Support Male Sexual Performance, Due to Undeclared, Potentially Hazardous Active Ingredient
  • From: U.S. Food & Drug Administration (FDA)
• Premium Edge, Diamond Naturals and 4health Dry Cat Food Formulas Voluntarily Recalled Due to Possibility of Low Levels of Thiamine (Vitamin B1)
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Completes Work on Two Animal Drug User Fee Programs
  • From: U.S. Food & Drug Administration (FDA)
• The March 2013 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses
  • From: U.S. Food & Drug Administration (FDA)
• RECALL: Bumble Bee 5-Ounce Chunk White Albacore And Chunk Light Tuna
  • From: FoodSafety.gov
• RECALL:Chicken of the Sea 5-Ounce Chunk White Albacore Tuna in Water
  • From: FoodSafety.gov
• Update of CVM's What's New - Premium Edge, Diamond Naturals and 4health Dry Cat Food Formulas Voluntarily Recalled Due to Possibility of Low Levels of Thiamine (Vitamin B1)
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Diggin' Your Dog Recalls Strippin' Chicks Pet Treats Distributed in Colorado and Nevada Due to Possible Salmonella Hazard
  • From: U.S. Food & Drug Administration (FDA)
• Diggin’ Your Dog Recalls Strippin' Chicks Pet Treats Distributed in Colorado and Nevada Due to Possible Salmonella Hazard
  • From: U.S. Food & Drug Administration (FDA)
• Diggin’ Your Dog Recalls Strippin' Chicks Pet Treats Due to Possible Salmonella Hazard
  • From: U.S. Food & Drug Administration (FDA)
• Proteja sus derechos y no se deje engañar
  • From: GobiernoUSA.gov
• Update of CVM's What's New - Updated Listing of Veterinary Feed Directive Distributor Notifications
  • From: U.S. Food & Drug Administration (FDA)
• Cambio de hora este domingo
  • From: GobiernoUSA.gov
• Tri-union Seafoods Expands Recall To Include Chunk Light Tuna In Oil Products
  • From: U.S. Food & Drug Administration (FDA)
• Steve’s Real Food Recalls Turducken Canine Recipe Patties Because of Posssible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Steve’s Real Food Recalls Turducken Canine Recipe Patties Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Acoso escolar cómo identificarlo y eliminarlo
  • From: GobiernoUSA.gov
• FDA issues draft guidance for manufacturers to accurately label medical products that are not made with natural rubber latex
  • From: U.S. Food & Drug Administration (FDA)
• Bumble Bee Foods Expands Voluntary Recall on Specific Codes of 5-Ounce Chunk White Albacore and Chunk Light Tuna Products Due to Loose Seals
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Ad-Tech Macro Micro Subdural Electrodes Class 1 recall: Concern the microelectrodes are defective and may cause injury to the brain.
  • From: FDA MedWatch
• Obtenga gratis una copia de la Guía del Consumidor
  • From: GobiernoUSA.gov
• Update of CVM's What's New - Small Entity Compliance Guide Available
  • From: U.S. Food & Drug Administration (FDA)
• Tri-Union Seafood Issues Voluntary Recall on Select 5-Ounce Chunk White Albacore Tuna in Water
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for March 06, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Programas de asistencia alimentaria
  • From: GobiernoUSA.gov
• Bumble Bee Foods Issues Voluntary Recall On Specific Codes Of 5-Ounce Chunk White Albacore And Chunk Light Tuna Products Due To Loose Seals
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Public Meetings with Food-Animal Producers and Veterinarians
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - ADUFA/AGDUFA Performance Reports
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - CVM's New Animal Drugs for Use in Feeds Workshop
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Cargill’s animal nutrition business conducts voluntary recall of select mineral product used in ruminant feed
  • From: U.S. Food & Drug Administration (FDA)
• Cargill’s animal nutrition business conducts voluntary recall of select mineral product used in ruminant feed
  • From: U.S. Food & Drug Administration (FDA)
• Kroger Recalls Select Wheat Bread Products in Idaho, Oregon and Washington States
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - VICH Guidances Available
  • From: U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: See’s Divinity Easter Egg with Walnuts (May Contain Peanut Butter)
  • From: FoodSafety.gov
• RECALL: Pork Products by Seven Sons, Heffron Farms, and Byron Center Meats
  • From: FoodSafety.gov
• CVM Updates - FDA Seeks Comments on IFT Report on Product Tracing Pilots
  • From: U.S. Food & Drug Administration (FDA)
• See’s Candies, Inc. Issues Allergy Alert on 1.7oz Divinity Egg with Walnuts, code L.A.D. 102/13
  • From: U.S. Food & Drug Administration (FDA)
• Food For Life issues Recall - Allergy Alert - Undeclared Allergen in Food For Life Ezekiel 4:9 Cereal
  • From: U.S. Food & Drug Administration (FDA)
• Usted y la Semana Nacional de Protección del Consumidor
  • From: GobiernoUSA.gov
• Protéjase del fraude qué saber y qué hacer
  • From: GobiernoUSA.gov
• FDA Hepatitis Update - Vicrelis (boceprevir) label changes
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Prezista (darunavir) label change - drug interaction information
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Intelence (etravirine) labeling updates
  • From: U.S. Food & Drug Administration (FDA)
• Cómo hacer un plan de negocios
  • From: GobiernoUSA.gov
• Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience Reports
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals March 2013 Update
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Uso adecuado de antibióticos
  • From: GobiernoUSA.gov
• Ad-Tech Medical Instrument Corporation Issues Global Recall of Macro Micro Subdural Electrodes
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Issues International Food Safety Capacity-Building Plan under the Food Safety Modernization Act
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - United Pet Group Inc. Recall
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Zachary Confections, Inc. Announces Recall of Zachary Chocolate Covered Marshmallow Eggs due to Possible Contamination and Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• United Pet Group Inc., Voluntarily Withdraws "Ultra Blend Gourmet Food for Parakeets," "eCotrition Grains & Greens Nutritional Supplement for Parakeets," "eCotrition Grains & Greens Nutritional Supplement for Canaries and Finches," and "eCotrition Grains & Greens Nutritional Supplement for Cockatiels" Due to Possible Salmonella Contamination
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 27, 2013
  • From: U.S. Food & Drug Administration (FDA)
• ¿Qué son los recortes automáticos?
  • From: GobiernoUSA.gov
• Cuide la salud del corazón con un examen cardiovascular
  • From: GobiernoUSA.gov
• Update of CVM's What's New - Letter to Kasel Associates Industries, Inc.
  • From: U.S. Food & Drug Administration (FDA)
• Lion Pavilion Issues Alert on Undeclared Sulfites in Grassplot Ginger Slices
  • From: U.S. Food & Drug Administration (FDA)
• Domega NY International Co., Ltd Issues an Alert on Undeclared Sulfites in Green Day Brand White Melon Seeds
  • From: U.S. Food & Drug Administration (FDA)
• Teleconferencia de inmigración
  • From: GobiernoUSA.gov
• FDA MedWatch - Sensipar (Cinacalcet Hydrochloride): Drug Safety Communication - FDA Suspends Pediatric Clinical Trials After Report Of Death
  • From: FDA MedWatch
• FDA approves Osphena for postmenopausal women experiencing pain during sex
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Approves Drug to Assist with Cattle Breeding Regimens
  • From: U.S. Food & Drug Administration (FDA)
• Affymax and Takeda Announce a Nationwide Voluntary Recall of All Lots of OMONTYS® (peginesatide) Injection
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lumenis VersaCut Tissue Morcellator: Class 1 Recall - Labeling Correction - Potential For Air Embolisms To Occur If Tubing Is Hooked Up Backwards
  • From: FDA MedWatch
• FDA approves Stivarga for advanced gastrointestinal stromal tumors
  • From: U.S. Food & Drug Administration (FDA)
• Olaax Corp. Issues a Nationwide Voluntary Recall of All Lots of Maxiloss Weight Advanced Softgels Dietary Supplement
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Hy-Vee Issues Voluntary Recall of Certain Dog Food Products
  • From: U.S. Food & Drug Administration (FDA)
• Herbalife Issues Allergy Alert due to Undeclared Milk Allergen in Instant Healthy Meal Nutritional Shake Mix Packets
  • From: U.S. Food & Drug Administration (FDA)
• King Arthur Flour Voluntarily Recalls Flour
  • From: U.S. Food & Drug Administration (FDA)
• Voluntary Recall of Dakota Specialty Milling Select Flours and Grain Blends
  • From: U.S. Food & Drug Administration (FDA)
• Hy-Vee Issues VoluntaryRecall of Certain Dog Food Products
  • From: U.S. Food & Drug Administration (FDA)
• Affymax and Takeda Announce a Nationwide Voluntary Recall of All Lots of OMONTYS® (peginesatide) Injection
  • From: U.S. Food & Drug Administration (FDA)
• Bruce Foods Corporation Expands Recall to Indiana of Food Club Red Enchilada Sauce Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 20, 2013
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Omontys (peginesatide) Injection by Affymax and Takeda: Recall of All Lots - Serious Hypersensitivity Reactions
  • From: FDA MedWatch
• Bruce Foods Corporation Recall Food Club Red Enchilada Sauce Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Heartland Brands Voluntarily Recalls Two Varieties of Granola Cereals
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - DePuy Orthopaedics LPS Diaphyseal Sleeve: Class I Recall - Taper Connection May Not Accommodate Physiologic Loads
  • From: FDA MedWatch
• FDA approves new treatment for late-stage breast cancer
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Recalls
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Kaytee Recalls Bird Treats and Greens Due to Possible Salmonella Contamination from Parsley Flakes
  • From: U.S. Food & Drug Administration (FDA)
• Kasel Associates Industries Recalling Certain Pet Treats Due to Salmonella Contamination
  • From: U.S. Food & Drug Administration (FDA)
• Undeclared Sulfites in Preserved Fruits
  • From: U.S. Food & Drug Administration (FDA)
• The Honest Kitchen® Voluntarily Recalls Limited Lots Of Verve®, Zeal®And Thrive® Products Due To Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Goldcoast Salads Expands Voluntary Recall to Include Additional Products Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Mondelēz Global LLC Conducts Nationwide Voluntary Recall of belVita Breakfast Biscuit Apple Cinnamon and Chocolate Varieties in the U.S. and Puerto Rico
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Guidance for Industry #108 Available
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Nutri-Vet, LLC Recalls Nutri-Vet and Nutripet Chicken Jerky Products Because Of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Nutri-Vet, LLC Recalls Nutri-Vet and Nutripet Chicken Jerky Products Because Of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Kasel Associated Industries Recalls All Products Manufactured at its Denver, Colorado Facility from April 20, 2012 thru September 19, 2012 Because of Possible Salmonella Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves new silicone breast implant
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves new silicone gel-filled breast implant
  • From: FDA Office of Women's Health
• Statement from Agriculture Secretary Tom Vilsack: World Organization for Animal Health Recommends United States' BSE Risk Status Be Upgraded
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Kasel Associated Industries Recall
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Voluntary Precautionary Recall Of Arnold, Brownberry, Earthgrains, Farm, Harmons, L’oven Fresh, Stroehmann and Sara Lee Multi-grain Breads and Sara Lee Thin Style Buns
  • From: U.S. Food & Drug Administration (FDA)
• Reumofan Plus USA, LLC and Reumofan USA, LLC is Voluntarily Recalling all lots of Reumofan Plus Tablets Due to Undeclared Drug Ingredients
  • From: U.S. Food & Drug Administration (FDA)
• MKG Provisions Voluntarily Recalls Atlantic Smoked Salmon Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Nature's Variety Issues Voluntarily Recall of One Batch of Instinct® Raw Organic Chicken Formula for Dogs & Cats Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Caring for Someone with the Flu
  • From: Flu.gov
• Decoty Coffee Company Inc. Issues Allergy Alert On Undeclared Soy In Decoty Taco Seasoning
  • From: U.S. Food & Drug Administration (FDA)
• Nature's Variety Issues Voluntarily Recall of One Batch of Instinct® Raw Organic Chicken Formula for Dogs & Cats Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Gilead Issues A Voluntary Recall Of One Lot Of Vistide® (CIDOFOVIR INJECTION) Due To Presence Of Particulate Matter
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vistide (Cidofovir Injection) by Gilead: Recall - Presence of Particulate Matter
  • From: FDA MedWatch
• Día de los Presidentes
  • From: GobiernoUSA.gov
• Pasos sencillos para crear un presupuesto
  • From: GobiernoUSA.gov
• What foods should pregnant women avoid? [Food Safe Fridays]
  • From: FoodSafety.gov
• FDA Hepatitis Update - Victrelis (boceprevir) label updates
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• AMPI Issues Allergy Alert for Undeclared Milk in Pudding
  • From: U.S. Food & Drug Administration (FDA)
• JS Pelmini OK Inc Issues Allergy Alert On Undeclared Milk And Soy In Potato Dumplings And Potato And Mushroom Dumplings
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GE Healthcare, LLC, Giraffe and Panda T-Piece Resuscitation Systems and Mask Resuscitation Systems: Class 1 Recall - Potential Reversal of Oxygen/Air
  • From: FDA MedWatch
• U.S. Marshals seize drug products distributed by a Florida company
  • From: U.S. Food & Drug Administration (FDA)
• Domega NY International CO., LTD. Issues An Alert On Undeclared Sulfites In Green Day Brand Dried Coconut
  • From: U.S. Food & Drug Administration (FDA)
• ZIP International Group LLC Recalls Dry Salted Fish Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 13, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Mantenga un corazón sano
  • From: GobiernoUSA.gov
• FDA MedWatch - St. Jude Medical, AMPLATZER TorqVue FX Delivery System: Class I Recall - Core Wire May Fracture
  • From: FDA MedWatch
• Salinas Firm Initiates A Precautionary Recall Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Extends Comment Period on AquAdvantage Salmon Documents
  • From: U.S. Food & Drug Administration (FDA)
• The February 2013 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• DZH Import & Export Inc. Issues an Alert on Undeclared Sulfites in Mountains Dried Mushroom
  • From: U.S. Food & Drug Administration (FDA)
• Pago electrónico de beneficios del Gobierno
  • From: GobiernoUSA.gov
• Ordene publicaciones gratis para mantener su corazón sano
  • From: GobiernoUSA.gov
• CVM Updates - FDA and JIFSAN Announce Online Training for Aquaculture Producers and Importers
  • From: U.S. Food & Drug Administration (FDA)
• Nestlé Prepared Foods Company Announces Voluntary Recall of LEAN CUISINE® Culinary Collection Mushroom Mezzaluna Ravioli
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• DZH Import & Export Inc. issues an alert on undeclared sulfites in Curiosity of Dashan Dried Mushroom
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Pomalyst for advanced multiple myeloma
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update _ Recent changes to the Reyataz (atazanavir sulfate) capsule labeling
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hamilton Medical, Inc., HAMILTON-T1 Ventilators with Software Versions 1.1.2 and Lower
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• UPDATED--Sprouters Northwest Expands Voluntary Recall to All Varieties of Sprouts Products, Wheatgrass, and Pea Shoots Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Muestre su cariño por el medio ambiente
  • From: GobiernoUSA.gov
• Update of CVM's What's New - 2013 Windows to Regulatory Research Internship Program
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Animal Drug Approvals Monthly Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA offers new guidance on developing drugs for Alzheimer’s disease
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Vet-LRN has changed its name to Vet-LIRN
  • From: U.S. Food & Drug Administration (FDA)
• GoldCoast Salads Voluntarily Recalls Blue Crab Spread Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for February 06, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Salud dental en los niños
  • From: GobiernoUSA.gov
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Domega NY International Co., Ltd Issues an Alert on Undeclared Sulfites in Green Day Brand Dried Coconut
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Annual Report on Antimicrobials Sold or Distributed for Food-Producing Animals in 2011
  • From: U.S. Food & Drug Administration (FDA)
• Flu Risks for People with Heart Disease
  • From: Flu.gov
• FDA approval of generic version of cancer drug Doxil is expected to help resolve shortage
  • From: U.S. Food & Drug Administration (FDA)
• R-Kane Products, Inc. Issues Allergy Alert On Undeclared Soy And Milk In Z Pro High Protein Supplement
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Final Rule on Administrative Detention of Food
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Tropical Nut and Fruit Co. Issues Allergy Alert on Undeclared Peanuts in “Chia Recharged Stix Mix” 5 Ounce Pouches
  • From: U.S. Food & Drug Administration (FDA)
• Whole Foods Market Voluntarily Recalls Prepared Food Items Made with Circle Sea Salmon Lox Trim in Two States Due to Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Sprouter Northwest Expands Recall to All Varieties of Sprouts Products, Wheatgrass, and Pea Shoots with Any Best by Dates and All Sizes Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Lo esencial para la temporada de impuestos de 2013
  • From: GobiernoUSA.gov
• HIV/AIDS Update - Prezista (darunavir) tablet and oral suspension: pediatric dosing
  • From: U.S. Food & Drug Administration (FDA)
• Free Heart Health Kit for Women
  • From: FDA Office of Women's Health
• FDA approves new drug for the chronic management of some urea cycle disorders
  • From: U.S. Food & Drug Administration (FDA)
• What is the norovirus? [Food Safe Fridays]
  • From: FoodSafety.gov
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Voluntary Field Correction Action Issued for GE Healthcare’s Resuscitation Systems with Blender Installed in GE Giraffe and Panda Infant Warmers
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Green Book On-line
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 30, 2013
  • From: U.S. Food & Drug Administration (FDA)
• 10 formas de ahorrar energía en el invierno
  • From: GobiernoUSA.gov
• FDA MedWatch - Vycor Viewsite Brain Access System (VBAS): Class 1 Recall - Unidentified Fiber Found on Device
  • From: FDA MedWatch
• Whole Foods Market Expands Its Recall Of Whole Catch Wild Alaskan Sockeye Salmon Because Of Possible Health Risk From Listeria
  • From: U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Tyzeka (telbivudine) label revisions
  • From: U.S. Food & Drug Administration (FDA)
• Adults need vaccines too!
  • From: Vaccines.gov
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Sprouter Northwest Recalls Alfafa, Brocco Sandwich Sprouts, Clover, Spicy Sprouts Because of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• The Hartz Mountain Corporation is voluntarily withdrawing its Hartz Chicken Chews and Hartz Oinkies Pig Skin Twists wrapped with Chicken for dogs
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
  • From: U.S. Food & Drug Administration (FDA)
• Cómo reciclar en el invierno
  • From: GobiernoUSA.gov
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Hartz Mountain Corporation Recall
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Lactated Ringers and 5 Percent Dextrose Injection, USP, 1000 ML, Flexible Containers: Recall - Due to Non-Sterility
  • From: FDA MedWatch
• Freedom Trading Issues a Voluntary Nationwide Recall of Super Power, a Product Marketed as a Dietary Supplement to Support Male Sexual Performance, Due to Undeclared, Potentially Hazardous Active Ingredient
  • From: U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Reorganization for the Foods and Veterinary Medicine Program
  • From: U.S. Food & Drug Administration (FDA)
• Whole Foods Market Recall Whole Catch Wild Alaskan Sockeye Salmon Because of Possible Health Risk from Listeria
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Labeling changes for Complera (emtricitabine/rilpivirine/tenofovir disoproxil fumarate)
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves three new drug treatments for type 2 diabetes
  • From: U.S. Food & Drug Administration (FDA)
• Proteja su computadora y sus datos de estafadores
  • From: GobiernoUSA.gov
• FDA approves Gleevec for children with acute lymphoblastic leukemia
  • From: U.S. Food & Drug Administration (FDA)
• First OTC Treatment for Overactive Bladder
  • From: FDA Office of Women's Health
• Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List
  • From: U.S. Food & Drug Administration (FDA)
• How do I safely prepare chicken? [Food Safe Fridays]
  • From: FoodSafety.gov
• FDA approves over-the-counter Oxytrol for Women to treat overactive bladder
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Samsca (tolvaptan): Drug Warning - Potential Risk of Liver Injury
  • From: FDA MedWatch
• Enforcement Report for January 23, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Specific Lots Of Hunt's Tomato Sauce Recalled For Can Defect
  • From: U.S. Food & Drug Administration (FDA)
• Winter eUpdate: New IUD, Safe Medication Use & More
  • From: FDA Office of Women's Health
• Voluntary Regional Recall Of Thomas', Sara Lee, Publix, And Weight Watchers Bagels
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves Exjade to remove excess iron in patients with genetic blood disorder
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Bausch and Lomb 27G Sterile Cannula Packed in Amvisc and Amvisc Plus Ophthalmic Viscosurgical Devices (OVD): Class I Recall - Cannulas May Leak or Detach From the Syringe
  • From: FDA MedWatch
• Flu Risks for Seniors
  • From: Flu.gov
• Annie's Voluntarily Recalls Annie's Homegrown Frozen Pizza Products
  • From: U.S. Food & Drug Administration (FDA)
• Sea un donante de sangre
  • From: GobiernoUSA.gov
• Evite estafas de inmigración
  • From: GobiernoUSA.gov
• HIV/AIDS Update - Kaletra (lopinavir/ritonavir) label update: drug interaction information
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Knott's Fine Foods Recalls Chicken Salad Sandwiches Because Of Possible Health Risk
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 16, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Día de Martin Luther King Jr.
  • From: GobiernoUSA.gov
• Cuatro años más de presidencia a partir del 20 de enero
  • From: GobiernoUSA.gov
• FDA MedWatch - Ferrous Sulfate Tablets, 325 mg Labeled as Rugby Natural Iron Supplement: Recall - Bottle May Contain Meclizine HCl 25 mg Tablets
  • From: FDA MedWatch
• When is my food thoroughly cooked? [Food Safe Fridays]
  • From: FoodSafety.gov
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• UPDATED - Allergy Alert – UNDECLARED EGGS in Kinnikinnick Foods Frozen Pie Crust
  • From: U.S. Food & Drug Administration (FDA)
• Advance Pharmaceutical Issues Nationwide Voluntary recall of one Lot (# 12G468) of Ferrous Sulfate Tablets, 325 mg, that may actually contain Meclizine HCl 25 mg tablets
  • From: U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Webinar “ Draft Guidance Vaginal Microbicides: Development for the Prevention of HIV Infection"
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Metal-on-Metal Hip Implants: Safety Communication - Updated Safety Recommendations
  • From: FDA MedWatch
• FDA approves Octaplas to treat patients with blood clotting disorders
  • From: U.S. Food & Drug Administration (FDA)
• Treating the Flu
  • From: Flu.gov
• FDA approves new seasonal influenza vaccine made using novel technology
  • From: U.S. Food & Drug Administration (FDA)
• Tome acción contra el radón
  • From: GobiernoUSA.gov
• Edificios federales promueven la ecología y los espacios abiertos
  • From: GobiernoUSA.gov
• A new direction for HealthCare.gov
  • From: Health Insurance Marketplace
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Boba Direct Issues Allergy Alert on Undeclared Milk in BD Flavored Powders
  • From: U.S. Food & Drug Administration (FDA)
• Homestead Creamery Artisan Cheese Removed from Store Shelves
  • From: U.S. Food & Drug Administration (FDA)
• Belmont Confections Issues Allergy Alert on Undeclared Peanuts in "Dymatize Nutrition, Elite Gourmet Bars" (Cookies & Cream and Fudge Brownie)
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - December 2012 Safety Labeling Changes includes 42 products with revisions to Prescribing Information
  • From: FDA MedWatch
• Lavarse las manos puede salvar vidas
  • From: GobiernoUSA.gov
• Update of CVM's What's New - Milo’s Kitchen® Voluntarily Recalls Chicken Jerky and Chicken Grillers Home-style Dog Treats
  • From: U.S. Food & Drug Administration (FDA)
• Milo’s Kitchen® Voluntarily Recalls Chicken Jerky and Chicken Grillers Home-style Dog Treats
  • From: U.S. Food & Drug Administration (FDA)
• Flu Season is Here--Take Action Now
  • From: Flu.gov
• Update of CVM's What's New - Updated Veterinary Master Files
  • From: U.S. Food & Drug Administration (FDA)
• Island Delights Volutarily Recalls Island Delights Coconut Haystack Candy Due to Undeclared Milk
  • From: U.S. Food & Drug Administration (FDA)
• How do I safely cook with eggs? [Food Safe Fridays]
  • From: FoodSafety.gov
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 09, 2013
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Mobius brand Mitosol (mitomycin for solution) Kit for Ophthalmic Use: Recall-May Not be Sterile
  • From: FDA MedWatch
• Update of CVM's What's New - FDA Announces Availability of the 2011 NARMS Retail Meat Annual Report
  • From: U.S. Food & Drug Administration (FDA)
• Giant & Martin's Alerts Customers To Voluntary Recall Of Ocean Beauty Seafood Smoked Salmon
  • From: U.S. Food & Drug Administration (FDA)
• The January 2013 MedSun Newsletter is now available...
  • From: U.S. Food & Drug Administration (FDA)
• FDA requires lower recommended doses for certain sleep drugs
  • From: FDA Office of Women's Health
• Mobius Therapeutics, LLC Issues a Voluntary Recall of Mitosol® (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use
  • From: U.S. Food & Drug Administration (FDA)
• Conozca cómo puede solicitar fondos del Gobierno para estudiar
  • From: GobiernoUSA.gov
• FDA MedWatch - Zolpidem Containing Products: Drug Safety Communication - FDA Requires Lower Recommended Doses
  • From: FDA MedWatch
• Update of CVM's What's New - 2012 ADUFA/AGDUFA Public Meeting Materials Available
  • From: U.S. Food & Drug Administration (FDA)
• Recall - Product Recall Because of Possible Listeria Monocytogenes Risk
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Update on Jerky Treats
  • From: U.S. Food & Drug Administration (FDA)
• Seguro Social: nuevos servicios por Internet
  • From: GobiernoUSA.gov
• Conozca más sobre el glaucoma
  • From: GobiernoUSA.gov
• FDA issues draft guidance on abuse-deterrent opioids
  • From: U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Cumulative Veterinary ADE Reports
  • From: U.S. Food & Drug Administration (FDA)
• Woodstock® Announces a Voluntary Recall for One Code Date of Mislabeled Woodstock Tamari Almonds Due to Undeclared Soy Allergen
  • From: U.S. Food & Drug Administration (FDA)
• Somersault Snack Co. Issues Allergy Alert on All Packages of Somersaults Cinnamon Crunch
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Southwest Ice Cream Specialties Conducts Voluntary Recall of ShurFine® Brand “Creamery Select Premium Ice Cream Dulce de Leche” 1.75 Quarts Ice Cream Because Package May Contain Praline Pecan Ice Cream Which May Contain Undeclared Allergens (Wheat, Soy and Pecans)
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fisher and Paykel Healthcare Reusable Breathing Circuit: Class I Recall - Pinholes in Tubes
  • From: FDA MedWatch
• Update of CVM's What's New - January 2013 Green Book Monthly Update
  • From: U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
  • From: U.S. Food & Drug Administration (FDA)
• ANDY CAPP’S HOT FRIES RECALLED DUE TO UNDECLARED SOY ALLERGEN
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Prevención del cáncer en las mujeres
  • From: GobiernoUSA.gov
• Are raw sprouts safe to eat? [Food Safe Fridays]
  • From: FoodSafety.gov
• FDA proposes new food safety standards for foodborne illness prevention and produce safety
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Gilster-Mary Lee Corp. Issues Allergy Alert on Undeclared Tree Nuts in Food Club Chocolate Chunk Brownie Mix.
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 02, 2013
  • From: U.S. Food & Drug Administration (FDA)
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Praxair Inc., Grab ‘n Go Vantage Portable Oxygen Cylinder Units: Class I Recall - Risk of Fire Inside Cylinder Unit
  • From: FDA MedWatch
• Allergy Alert – Undeclared Eggs in Kinnikinnick Foods Frozen Pie Crust
  • From: U.S. Food & Drug Administration (FDA)
• Cómo escoger una agencia de asesoría de crédito
  • From: GobiernoUSA.gov
• HIV/AIDS Update - Approval of Fulyzaq (crofelemer) to relieve symptoms of diarrhea in HIV/AIDS patients taking antiretroviral therapy
  • From: U.S. Food & Drug Administration (FDA)
• ¡Feliz 2013!
  • From: GobiernoUSA.gov
• Looking Forward to 2013
  • From: HealthCare.gov
• Vaccines and Related Biological Products Advisory Committee Update
  • From: U.S. Food & Drug Administration (FDA)
• Despídase del 2012 de manera segura
  • From: GobiernoUSA.gov
• Update of CVM's What's New
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves first anti-diarrheal drug for HIV/AIDS patients
  • From: U.S. Food & Drug Administration (FDA)
• Procesadora de Productos Marinos Delifish S.A. Recalls Product Because Of Possible Listeria Monocytogenes Risk
  • From: U.S. Food & Drug Administration (FDA)
• FDA approves first drug to treat multi-drug resistant tuberculosis
  • From: U.S. Food & Drug Administration (FDA)
• Urgent: ADM Alliance Nutrition Recalling MoorMan’s® ShowTec® 18 Elite Lamb Feed
  • From: U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 26, 2012
  • From: U.S. Food & Drug Administration (FDA)
• Si va al volante, vaya sobrio
  • From: GobiernoUSA.gov
• Resoluciones de Año Nuevo: cúmplalas
  • From: GobiernoUSA.gov
• FDA MedWatch - GE Healthcare T-Piece Circuits for the Giraffe and Panda Resuscitation Systems: Class I Recall – Failure to Achieve the Desired Inspiratory Pressure During Ventilation
  • From: FDA MedWatch
• What should I know about food poisoning? [Food Safe Fridays]
  • From: FoodSafety.gov
• FDA MedWatch - Zimmer Spine - PEEK Ardis Inserter: Class I Recall – Risk of Implant Breakage
  • From: FDA MedWatch
• Drug Shortages Update
  • From: U.S. Food & Drug Administration (FDA)
• Voluntary Worldwide Field Corrective Action Issued for the T-piece Circuit used on GE Healthcare’s Giraffe and Panda
  • From: U.S. Food & Drug Administration (FDA)