FDA News
[Prev Page][Next Page]
- FDA MedWatch - December 2013 Drug Safety Labeling Changes includes 39 products with revisions to Prescribing Information
- FDA approves Mekinist in combination with Tafinlar for advanced melanoma
- From: U.S. Food & Drug Administration (FDA)
- Flat Creek Farm & Dairy Recalls Cheese Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for January 08, 2014
- From: U.S. Food & Drug Administration (FDA)
- The January 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first gel for sealing corneal incision after cataract surgery
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Covidien, Puritan Bennett 840 Series Ventilator - Software Problem
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals January 2014 Update
- From: U.S. Food & Drug Administration (FDA)
- L.M. Noodle Company Issues Allergy Alert on Undeclared Wheat Flour, Soy Flour Whey and Milk in Butterballs
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Farxiga to treat type 2 diabetes
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Sodium Phosphate Over-the-Counter Products: Drug Safety Communication - Possible Harm From Exceeding Recommended Dose
- FDA MedWatch - Truebalance and Truetrack Blood Glucose Meters by Nipro Diagnostics: Recall - Incorrect Factory-set Measure
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Tonia’s Biscotti II LLC Issues Allergy Alert on Undeclared Wheat, Milk, and Soy in Tonia’s Biscotti Sampler Bags, Lemon Biscotti Dipped in White Chocolate Bags, and Individually Wrapped Biscotti of All Flavors
- From: U.S. Food & Drug Administration (FDA)
- Nipro Diagnostics, Inc. Initiates Voluntary Recall of Certain TRUEbalance and TRUEtrack Blood Glucose Meters
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - SafeSpout and SafeShower Filtration Products by Nephros: Class I Recall - Exposure to Bacteria or Virus
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Pida gratis su informe de crédito
- Medical Device Safety and Recalls: GE Healthcare, LLC - Multi Absorber Original, Disposable - Model M1173310
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Nephros Filtration Products
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - CLINIMIX and CLINIMIX E Injection/Baxter: Recall - Particulate Matter in Products
- Baxter Initiates Nationwide Voluntary recall Of Select Lots of Premix Parenteral Nutrition
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for January 01, 2014
- From: U.S. Food & Drug Administration (FDA)
- Una buena salud es clave para alcanzar sus metas
- Update of CVM's What's New - Updated Listings - Medicated Feed Mill Licenses/Veterinary Feed Directive Distributors
- From: U.S. Food & Drug Administration (FDA)
- Deseo Rebajar Inc. Inicia un Recogido Voluntario del Producto en Cápsulas “Burn 7” Debido a Ingrediente Activo sin Declarar
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - The Ins and Outs of Extra-Label Drug Use in Animals: A Resource for Veterinarians
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - CO2 Multi Absorber by Vital Signs Devices: Field Corrective Action - Loss of Anesthetic Gases, Ventilation and Oxygenation
- Campbell Recalls 300 Cases of Prego Traditional Italian Sauce Due to a Risk of Spoilage
- From: U.S. Food & Drug Administration (FDA)
- The Cultured Kitchen Voluntarily Recalls Cashew Cheese Due To Possible Risk Of Contamination From Salmonella
- From: U.S. Food & Drug Administration (FDA)
- Voluntary Field Corrective Action Initiated for Vital Signs Device’s CO2 Multi Absorber Due to a Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Ayuda financiera para estudiantes
- Consejos para una buena salud financiera
- Recursos y programas para personas de la tercera edad
- Update of CVM's What's New - Food Safety Modernization Act and Animal Feed
- From: U.S. Food & Drug Administration (FDA)
- Giant Eagle Issues Allergy Alert On Undeclared Peanut Allergen In Candy Place Chocolate Santas
- From: U.S. Food & Drug Administration (FDA)
- Zip International Group LLC Recalls FOSFOREL Herring Fillet in Oil Due to Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Baxter 5 Percent Dextrose Injection, USP And 0.9 Percent Sodium Chloride Injection, USP Intravenous (IV) Solutions: Recall - Particulate Matter In Solution
- Baxter Initiates Worldwide Voluntary Recall Of Select Lots Of 5 percent Dextrose Injection, USP And 0.9 percent Sodium Chloride Injection, USP Intravenous (IV) Solutions
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 26, 2013
- From: U.S. Food & Drug Administration (FDA)
- Deseo Rebajar Inc. Issues Voluntary Recall of Burn 7 Capsules Due to Undeclared Active Ingredient
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Lidocaine HCl Injection 2%, 5 ml Vial by Hospira: Recall - Presence of Particulate Matter
- Hospira Issues a Voluntary Nationwide Recall of One Lot of Lidocaine HCl Injection, USP, 2%, 5 Ml in 5 Ml Vial, Due to Presence of Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Muscle Growth Product Called Mass Destruction: FDA Health Risk Warning - Undeclared Ingredients
- FDA warns consumers not to use muscle growth product
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Tretten to treat rare genetic clotting disorder
- From: U.S. Food & Drug Administration (FDA)
- Spokane Produce, Inc. Voluntarily Recalls Victor™ Toasted Sesame Hummus Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Concertos in Chocolate Issues Allergy Alert on Milk in Solid Milk Chocolate Santa
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - New Isentress (raltegravir) dosage form: oral suspension
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Changes to the Baraclude (entecavir) package and label
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - New PegIntron Selectdose
- From: U.S. Food & Drug Administration (FDA)
- Make 2014 Your Healthiest Year Yet
- From: FDA Office of Women's Health
- Conozca por dónde anda Papá Noel durante la Nochebuena
- FDA MedWatch - Abrams Royal Pharmacy Sterile Products - Recall - Lack of Sterility Assurance
- Abrams Royal Pharmacy Issues Voluntary Nationwide Recall of All Lots of Unexpired Sterile Products Due to Lack of Sterility Assurance
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 18, 2013
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Anoro Ellipta to treat chronic obstructive pulmonary disease
- From: U.S. Food & Drug Administration (FDA)
- FDA and European Medicines Agency launch generic drug application inspections initiative
- From: U.S. Food & Drug Administration (FDA)
- 10 consejos para las fiestas
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Methylphenidate ADHD Medications: Drug Safety Communication - Risk of Long-lasting Erections
- Megabusiness LLC Issues Alert on Undeclared Sulfites in Del Campo Papa Seca / DRY Potato 24x14 oz.
- From: U.S. Food & Drug Administration (FDA)
- Bee International Expands Allergy Alert on Undeclared Egg in "Sweet Spots"
- From: U.S. Food & Drug Administration (FDA)
- Prevenga la gripe en esta temporada
- Lock up your medicines to protect children and teens this holiday season
- From: U.S. Food & Drug Administration (FDA)
- Cómo preparar comidas saludables para las fiestas
- Blooming Import Inc. Issues an Alert on Undeclared Sulfites in Farmer Brand Dried Lily Flowers
- From: U.S. Food & Drug Administration (FDA)
- Stone Independent Research, Inc. Issues Allergy Alert on Undeclared Milk in One Lot of Zanocap Capsules
- From: U.S. Food & Drug Administration (FDA)
- Stone Independent Research, Inc. Issues Allergy Alert on Undeclared Milk in EnhanceRx Dietary Supplement
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Food Safety Modernization Act and Animal Feed
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Soliris (Eculizumab) Concentrated Solution for Intravenous Infusion by Alexion: Recall - Visible Particles
- Medical Device Safety and Recalls: FDA Announces Improvements To The Medical Device Recalls Database
- From: U.S. Food & Drug Administration (FDA)
- Alexion Provides Update on Previously Communicated November 2013 Voluntary Nationwide Recall of Two Lots of Soliris (eculizumab) Concentrated Solution for Intravenous Infusion
- From: U.S. Food & Drug Administration (FDA)
- Bee International Issues Allergy Alert on Undeclared Egg in "Sweet Spots"
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update – changes to Complera (emtricitabine, rilpivirine, tenofovir disoproxil fumarate) labeling for HIV/AIDS
- From: U.S. Food & Drug Administration (FDA)
- Publicaciones en español gratis para un año más saludable
- Pin Hsiao & Associates, LLC. Issues Allergy Alert on Undeclared Walnuts in Gluten Free Blueberry Mini Muffins - 12 pk.
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for December 11, 2013
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Nipple Aspirate Test: Safety Communication - Breast Cancer Screening Test Is Not An Alternative To Mammography
- Blooming Import Inc. Issues an Alert on Undeclared Sulfites in Golden Lion Brand Dried Ziziphus Jujuba Mill (Dried Dates)
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Breast Cancer Screening - Nipple Aspirate Test Is Not An Alternative To Mammography
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market Mid-Atlantic Region Recalls Spinach Dip Due to Undeclared Egg
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Answers Your Questions about Fish Drugs
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Judicious Use of Antimicrobials
- From: U.S. Food & Drug Administration (FDA)
- Health Matters America Inc. Issues an Allergy Alert on Undeclared Milk in Organic Traditions Brand Dark Chocolate Hazelnuts, Dark Chocolate Hazelnuts with Chili, Dark Chocolate Almonds, and Dark Chocolate Almonds with Chili.
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first generic versions of antidepressant drug Cymbalta
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Takes Significant Steps to Address Antimicrobial Resistance
- From: U.S. Food & Drug Administration (FDA)
- FDA takes significant steps to address antimicrobial resistance
- From: U.S. Food & Drug Administration (FDA)
- Cómo hacer envíos para Navidad por correo postal
- The December 2013 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Approval of Sovaldi (sofosbuvir) tablets for the treatment of chronic hepatitis C
- From: U.S. Food & Drug Administration (FDA)
- El agua potable y su salud
- FDA approves first drug treatment for Peyronie’s disease
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - November 2013 Drug Safety Labeling Changes includes 27 products with revisions to Prescribing Information
- Enforcement Report for December 04, 2013
- From: U.S. Food & Drug Administration (FDA)
- Todos tienen que tener un seguro de salud en el 2014
- Infórmese sobre leyes que prohíben discriminación por discapacidad
- Update of CVM's What's New - Animal Drug Approvals December 2013 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Philips HeartStart FRx, HeartStart HS1 Home, and HeartStart HS1 OnSite Automated External Defibrillators (AED)
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Cargill Conducts Voluntary Recall of Select Nutrena® NatureWise® Meatbird and Chick Starter Feed
- From: U.S. Food & Drug Administration (FDA)
- Cargill Conducts Voluntary Recall of Select Nutrena® NatureWise® Meatbird and Chick Starter Feed
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - HeartStart Automated External Defibrillators (AED) From Philips Healthcare: Safety Communication - Failure Of An Electrical Component That Could Cause AEDs To Fail To Deliver Appropriate Shock
- FDA issues safety communication on HeartStart automated external defibrillators from Philips Healthcare
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Addresses Continued Shortage of Drug Used to Treat Heartworm Infection in Dogs
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Onfi (clobazam): Drug Safety Communication - Risk of Serious Skin Reactions
- Huxtable’s Kitchen Issues Voluntary Allergy Alert on Undeclared Allergens in Butternut Squash & Creamed Spinach Gratin
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Resolved Drug Shortage for Xylazine
- From: U.S. Food & Drug Administration (FDA)
- Recomendaciones para comprar juguetes seguros
- IQ Formulations Issues a Voluntary Recall of HYDRAVAX Dietary Supplement Due to Possible Undeclared Ingredient
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - FreeStyle and FreeStyle Lite Blood Glucose Test Strips by Abbott: Recall - Erroneously Low Blood Glucose Results
- Abbott Issues Voluntary Recall of Certain FreeStyle® and FreeStyle Lite® Blood Glucose Test Strips in the United States
- From: U.S. Food & Drug Administration (FDA)
- Flat Creek Farm and Dairy Recalls Heavenly Blue Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 27, 2013
- From: U.S. Food & Drug Administration (FDA)
- No maneje tomado
- FDA MedWatch - Nitroglycerin in 5% Dextrose Injection by Baxter: Recall - Particulate Matter
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Baxter Initiates Nationwide Voluntary Recall of One Lot of Nitroglycerin in 5% Dextrose Injection
- From: U.S. Food & Drug Administration (FDA)
- Zip International Group LLC Recalls Herring Fillet in Oil Due to Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA study helps provide an understanding of rising rates of whooping cough and response to vaccination
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Spacelabs Healthcare, Inc., Spacelabs Anesthesia Workstations and Service Kits
- From: U.S. Food & Drug Administration (FDA)
- Proteja su información al comprar por Internet
- FDA MedWatch - Spacelabs Healthcare, Inc., Spacelabs Anesthesia Workstations and Service Kits: Class I Recall - Bag-to-Vent Switch in CAS I/II Absorbers May Fail
- FDA MedWatch - CLR Medicals International Inc. Viscoelastic Products: Recall - Quality System Deficiencies And Lack Of Premarket Approval (PMR)
- CLR Medicals International Inc. Issues Nationwide Recall of Viscoelastic Products
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Hospira GemStar Infusion System: Class I Recall - Pressure Sensor Calibration Drift
- FDA requires removal of certain restrictions on the diabetes drug Avandia
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Rosiglitazone-containing Diabetes Medicines: Drug Safety Communication - Removal of Some Prescribing and Dispensing Restrictions
- Medical Device Safety and Recalls: Hospira Inc., GemStar Infusion System - Pressure Sensor Calibration Drift
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Olysio (simeprevir) for the treatment of chronic hepatitis C in combination antiviral treatment
- From: U.S. Food & Drug Administration (FDA)
- ¡Feliz Día de Acción de Gracias!
- Jayone Food Issues Voluntary Alert on Undeclared Peanuts in Dried Seaweed Salad
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 20, 2013
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Meridian Medical Technologies Auto-Injectors: Extension of Expiration Dates
- FDA approves Nexavar to treat type of thyroid cancer
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first adjuvanted vaccine for prevention of H5N1 avian influenza
- From: U.S. Food & Drug Administration (FDA)
- Gasolina: encuentre los mejores precios
- Update of CVM's What's New - Veterinary Medicine Advisory Committee Disbands
- From: U.S. Food & Drug Administration (FDA)
- Beneficios del Gobierno: búsqueda fácil y rápida
- Check medicines to avoid taking too much acetaminophen this cold and flu season
- From: U.S. Food & Drug Administration (FDA)
- Deseo Rebajar Inc. Issues Voluntary Puerto Rico Recall of Adipotrim XT Due to Underclared Fluoxetine
- From: U.S. Food & Drug Administration (FDA)
- Marina's German Bakery Issues Allergy Alert on Undeclared Almonds, Walnuts, and Hazelnuts in Pastry Products
- From: U.S. Food & Drug Administration (FDA)
- Día Nacional de No Fumar
- FDA MedWatch - Lexiscan (regadenoson) and Adenoscan (adenosine): Drug Safety Communication - Rare but Serious Risk of Heart Attack and Death
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List
- From: U.S. Food & Drug Administration (FDA)
- Tendex Issues Voluntary Nationwide Recall of P-Boost, NatuRECT Due to Undeclared Active Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Public Meeting Agendas Available
- From: U.S. Food & Drug Administration (FDA)
- Blount Fine Foods Voluntary Recall of “Wegmans New England Clam Chowder” Due to Possible Undeclared Crab Allergen
- From: U.S. Food & Drug Administration (FDA)
- Recall expanded to include: Raspberry Lemonade OxyELITE Pro Super Thermo Powder
- From: U.S. Food & Drug Administration (FDA)
- Planifique un Día de Acción de Gracias libre de riesgos para su salud
- Medical Device Safety and Recalls: Medtronic Interventional Guidewires and ATTAIN HYBRID® Guidewires
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Food Safety Modernization Act and Animal Feed Update
- From: U.S. Food & Drug Administration (FDA)
- Fossil Fuel Products, LLC, Issues Voluntary Nationwide Recall of “RezzRX” Due to Undeclared Active Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Jobbers Wholesale Issues Voluntary Recall of Rhino 5 Plus, Maxtremezen and Extenzone Marketed as a Dietary Supplement Due to the Presence of Undeclared Drug Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Consejos para ahorrar energía durante el invierno
- Diabetes: cómo controlarla
- New Reliance Traders, Inc.- Voluntarily Recalls Hashmi Surma Special Eyeliner Due to Elevated Lead Levels
- From: U.S. Food & Drug Administration (FDA)
- S&M Enterprise Issues Allergy Alert for Fruit of Wolfberry, 12 Oz Plastic Bag due to Undeclared Sulfites
- From: U.S. Food & Drug Administration (FDA)
- Nature's Pharmacy and Compounding Center Issues Voluntary Recall of All Sterile Compounded Products Distributed Within North Carolina Due to Lack of Sterility Assurance
- From: U.S. Food & Drug Administration (FDA)
- La Boulange Cafe & Bakery Issues an Allergy Alert for Undeclared Allergen (Hazelnut) in Product Inadvertently Mislabeled as Soft Caramel Jam
- From: U.S. Food & Drug Administration (FDA)
- FDA Classifies Medtronic's Worldwide Voluntary Field Action on Guidewires as Class I Recall
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Nature's Pharmacy and Compounding Center Sterile Compounded Products: Recall - Lack of Sterility Assurance
- FDA MedWatch - Medtronic Guidewires: Recall - Potential For Coating On Surface To Delaminate And Detach
- FDA MedWatch - October 2013 Safety Labeling Changes includes 68 products with revisions to Prescribing Information
- Dele una mano al medio ambiente
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Vitality Research Labs, LLC, Issues Immediate Voluntary Nationwide Recall of "VitaliKOR Fast Acting" Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Crunch Pak Issues Voluntary Recall of Limited Quantities of Crunch Pak Brand Apple Slices Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 13, 2013
- From: U.S. Food & Drug Administration (FDA)
- The November 2013 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- FDA approves medical device to treat epilepsy
- From: U.S. Food & Drug Administration (FDA)
- Uso adecuado de antibióticos
- Bailey's Choice Recalls Chicken Treats Because of Possible Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- 3 Fellers LLC Issues an Allergy Alert for Undeclared Allergen (Almonds) in Chocolate Cream Pies
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Over-the-Counter Topical Antiseptic Products: Drug Safety Communication - FDA Requests Label Changes and Single-Use Packaging to Decrease Risk of Infection
- Update of CVM's What's New - Public Meeting Agenda: FSMA Proposed Rule for Preventive Controls for Animal Food
- From: U.S. Food & Drug Administration (FDA)
- Recursos para cuidadores de pacientes con enfermedad de Alzheimer
- FDA approves Imbruvica for rare blood cancer
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Atossa Genetics Mammary Aspiration Specimen Cytology Test (MASCT) System Kit and the ForeCYTE Breast Health Test
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market® Recalls Ready-To-Eat Grain Salads
- 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)
- Vega Issues Voluntary Withdrawal of Vega One Nutritional Shakes and Vega Sport Performance Protein Product Due to Traces of the Antibiotic Chloramphenicol
- From: U.S. Food & Drug Administration (FDA)
- Plum Organics Voluntarily Recalls a Range of Pouch Products
- From: U.S. Food & Drug Administration (FDA)
- USPlabs LLC Announces a Recall of OxyElite Pro Dietary Supplements Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Palmer Candy Company Voluntarily Recalls HyVee Chocolate Caramel Clusters and HyVee Chocolate Covered Caramels Due to Undeclared Peanut Allergen
- From: U.S. Food & Drug Administration (FDA)
- Atherstone Foods Voluntarily Recalls Salads and Wraps Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - OxyElite Pro Dietary Supplements by USP Labs: Recall - Products Linked to Liver Illnesses
- USPlabs LLC recalls OxyElite Pro dietary supplements; products linked to liver illnesses
- From: U.S. Food & Drug Administration (FDA)
- Celebre el Día de los Veteranos
- Medical Device Safety and Recalls: Pentax Medical Company, PENTAX Gas/Water Valve, Model OF-B194
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Baylis Medical TorFlex Transseptal Guiding Sheath Kit
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first generic versions of Aciphex delayed-release tablets to treat GERD
- From: U.S. Food & Drug Administration (FDA)
- Garden-Fresh Foods, Inc. Expands Recall Due to Potential Contamination with Listeria Monocytogenes
- From: U.S. Food & Drug Administration (FDA)
- Garden-Fresh Foods, Inc. Expanded Recalls on Specific Packages of Products Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA takes action to speed safety information updates on generic drugs
- From: U.S. Food & Drug Administration (FDA)
- Tenga cuidado al comprar medicinas por Internet
- Update of CVM's What's New - Bailey’s Choice Expands Product Recall of Dog Treats in Georgia
- From: U.S. Food & Drug Administration (FDA)
- Bailey’s Choice Expands Product Recall of Dog Treats in Georgia
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 06, 2013
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Baylis Medical TorFlex Transseptal Guiding Sheath Kit: Class I Recall - Sheath Could Remove Particulate
- FDA MedWatch - Low Molecular Weight Heparins: Drug Safety Communication - Recommendations to Decrease Risk of Spinal Column Bleeding and Paralysis
- Update of CVM's What's New - Get the Facts! Raw Pet Food Diets can be Dangerous to You and Your Pet
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Gourmet Express LLC. Voluntarily Recalls 32 Ounce Packages of "Fusia Chicken Lo Mein" and 21 Ounce Packages Of “Bremer 3 Cheese Chicken” and “Bremer Garlic Shrimp" Due to Possible Undeclared Eggs
- From: U.S. Food & Drug Administration (FDA)
- Qué hacer si es víctima del robo de identidad
- Update of CVM's What's New - Pain Medicines for Pets: Know the Risks
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Edwards Lifesciences LLC, EMBOL-X Glide Protection System: Class I Recall - Deformed Cannula Tip
- Medical Device Safety and Recalls: Edwards Lifesciences LLC, EMBOL-X Glide Protection System
- From: U.S. Food & Drug Administration (FDA)
- ¿Ya se vacunó contra la gripe?
- Reser’s Fine Foods, Inc. Voluntarily Expands Recall of Refrigerated Ready-to-Eat Products Due to Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals November 2013 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Garden-Fresh Foods, Inc. Expanded Recalls on Specific Packages of Products Because of Possible Health Risk Recall Class I
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Food Safety Modernization Act (FSMA) - UPDATE
- From: U.S. Food & Drug Administration (FDA)
- FDA: Janssen Pharmaceuticals, Inc. to plead guilty and pay over $1.6 billion to resolve allegations of misbranding and filing false claims for its schizophrenia drug Risperdal
- From: U.S. Food & Drug Administration (FDA)
- Ghiringhelli Specialty Foods Issues Voluntary Alert on Undeclared Allergens in Caesar Salad
- From: U.S. Food & Drug Administration (FDA)
- Dutch Treat Salads, LLC Voluntarily Recalls Mexicali Dip Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Perrigo Initiates Nationwide Voluntary Product Recall of Acetaminophen Infant Suspension Liquid, 160 mg/5 mL, Due to a Potential Defect with the Co-packaged Oral Syringe
- From: U.S. Food & Drug Administration (FDA)
- Winn-Dixie Expands Recall to Include Spinach Antipasta Salad
- From: U.S. Food & Drug Administration (FDA)
- Winn-Dixie Issues Recall on Pre-Prepared Broccoli Crunch Salad
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Perrigo Acetaminophen Infant Suspension Liquid: Recall - Potential Defect with Co-packaged Oral Syringe
- Cómo funciona el Gobierno de Estados Unidos
- FDA MedWatch - September 2013 Safety Labeling Changes includes 49 products with revisions to Prescribing Information
- Cómo identificar la adicción a los juegos de azar
- Reser's
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Index of Legally Marketed Unapproved New Animal Drugs for Minor Species
- From: U.S. Food & Drug Administration (FDA)
- Cambio de hora este 3 de noviembre
- FDA approves Gazyva for chronic lymphocytic leukemia
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA Veterinarian - November 1, 2013
- From: U.S. Food & Drug Administration (FDA)
- PENTAX Medical Company Issues Voluntary Nationwide Recall of OF-B194 Gas/ Water Valve
- From: U.S. Food & Drug Administration (FDA)
- World Class Distribution Issues Voluntary Allergy Alert On Undeclared Soy In Southwest Salad
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 30, 2013
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Presentation on the Proposed Rule for Preventive Controls for Food for Animals
- From: U.S. Food & Drug Administration (FDA)
- FDA takes two important actions on drug shortages
- From: U.S. Food & Drug Administration (FDA)
- Firms Initiate Secondary Recall in Response to the Expansion of Reser’s Fine Foods Recall
- From: U.S. Food & Drug Administration (FDA)
- Garden Fresh Foods, Inc. Expands Recalls on Specific Packages of Products Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Changes to Incivek (telaprevir) product labeling
- From: U.S. Food & Drug Administration (FDA)
- BI-LO Issues Recall Of Spinach Antipasti Salad In One Store
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - CVM Clarifies Use of Melengestrol Acetate in Combination with Monensin and Tylosin, and with Monensin Alone, in Animal Feed
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Hepatitis B reactivation with certain immune-suppressing and anti-cancer drugs
- From: U.S. Food & Drug Administration (FDA)
- Tennessee and Maryland Firms Initiate Recall Based on Reser's Fine Foods Recall
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Revised draft guidance on clinical development of treatment for chronic hepatitis C
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - How to Report a Complaint about Jerky Pet Treats
- From: U.S. Food & Drug Administration (FDA)
- Boston Salads and Prepared Foods Recalling Ready-To- Eat Products Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Kraft Voluntarily Recalls Some Varieties of Kraft And Polly-O String Cheese And String Cheese Twists Due to Premature Spoilage
- From: U.S. Food & Drug Administration (FDA)
- Reser's Fine Foods, Inc. Voluntarily Expands Recall of Refrigerated Ready-to-Eat Products Due to Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA approves extended-release, single-entity hydrocodone product
- From: U.S. Food & Drug Administration (FDA)
- FDA approves second brain imaging drug to help evaluate patients for Alzheimer’s disease, dementia
- From: U.S. Food & Drug Administration (FDA)
- Cómo prevenir el envenenamiento por plomo
- CVM Updates - FDA Issues Proposed Rule under FSMA to Improve Safety of Food for Animals
- From: U.S. Food & Drug Administration (FDA)
- Mercado de Seguros Médicos: ¿qué ofrece y cómo puede inscribirse?
- Violencia doméstica: qué puede hacer
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News 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)
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
- From: U.S. Food & Drug Administration (FDA)
- Kashmir Crown Baking LLC Issues Allergy Alert on Undeclared Eggs on KCB Pista Khatie
- From: U.S. Food & Drug Administration (FDA)
- NatureMost Laboratories Issues Allergy Alert On Undeclared (Allergen) In Product
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 09, 2013
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 16, 2013
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 23, 2013
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - MedStream Programmable Infusion Pump and Refill Kits by Codman and Shurtleff: Class 1 Recall - Drug Over Infusion
- Update of CVM's What's New - Prevent Heartworms in Pets Year-Round
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Announces Minor Use/Minor Species (MUMS) Grant Program Request for Applications
- From: U.S. Food & Drug Administration (FDA)
- Reser’s Fine Foods, Inc. Recalls Refrigerated Ready-to-Eat Products Due to Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA to complete phase-out of chlorofluorocarbon inhalers
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Draeger Medical Fabius Series Anesthesia Machines - Failure of Automatic Ventilation
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Codman and Shurtleff MedStream Programmable Infusion Pump and Refill Kits - Drug Over Infusion
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Guidance Available
- From: U.S. Food & Drug Administration (FDA)
- Sunny Pine Farms Recalls Chevre Cheese Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: GE Healthcare – Engström Ventilator and Aespire View, Aisys, Avance, and Avance CS2 Anesthesia Machines
- From: U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Releases Progress Report on Jerky Pet Treat Investigation
- From: U.S. Food & Drug Administration (FDA)
- Incripción abierta de Medicare
- Update of CVM's What's New - Guidance Available
- From: U.S. Food & Drug Administration (FDA)
- Price Chopper Supermarkets Recalls Coconut Custard Pies
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Specialty Medicine Compounding Pharmacy Certain Unexpired Compounded Sterile Products: Recall - Particulate Matter Found in Vials
- Medical Device Safety and Recalls: CareFusion 211, Inc., AVEA Ventilators, All Models
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: H and H Medical Corporation (formerly H and H Associates) Emergency Cricothyrotomy Kit – Cuff Balloon May Not Function as Intended
- From: U.S. Food & Drug Administration (FDA)
- Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.25% Marcaine™ (Bupivacaine HCL Injection, USP), 75mg/30ml, Single-Dose - Preservative Free Vial Due to Presence of Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 02, 2013
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Bard LifeStent Solo Vascular Stent: Class 1 Recall - Failure to Deploy
- Cáncer de mama: prevención y ayuda
- FDA approves Opsumit to treat pulmonary arterial hypertension
- From: U.S. Food & Drug Administration (FDA)
- Vaccines and Related Biological Products Advisory Committee Update
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Bard LifeStent Solo Vascular Stent - Failure to Deploy Stent
- From: U.S. Food & Drug Administration (FDA)
- Hágase la prueba de detección del VIH
- Fahman Enterprises Inc. - Recalls Pran Brand Turmeric Powder Due to Elevated Levels of Lead
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Albuterol Sulfate Inhalation Solution, 0.083 percent (Nephron Pharmaceuticals): Recall - Aseptic Processing Simulation Results
- FDA MedWatch - St. Jude Amplatzer Atrial Septal Occluder (ASO): Safety Communication - Reports of Tissue Erosion
- Medical Device Safety and Recalls: Rare Serious Erosion Events Associated with St. Jude Amplatzer Atrial Septal Occluder (ASO)
- From: U.S. Food & Drug Administration (FDA)
- Nephron Pharmaceuticals Corporation Announces Voluntary Recall of Albuterol Sulfate Inhalation Solution, 0.083%
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals October 2013 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Mandy Star Trading Inc. Is Issuing an Alert on Undeclared Sulfites in "Good Taste" Brand Plum
- From: U.S. Food & Drug Administration (FDA)
- Yoder's Country Market, Inc. Issues Allergy Alert on Gift Boxes Containing 11 oz. Bags of Honey Roasted Peanuts Distributed in December 2012
- From: U.S. Food & Drug Administration (FDA)
- Voluntary Field Corrective Action Issued for GE Healthcare’s Engström Ventilator and Aespire View, Aisys, and Avance Anesthesia Machines
- From: U.S. Food & Drug Administration (FDA)
- Best Value, Inc., Recalls PRAN Bran Turmeric Powder Due to Elevated Levels of Lead
- From: U.S. Food & Drug Administration (FDA)
- B. Braun Medical Inc. Issues Voluntary Nationwide Recall of Lot H3A744, 1 gram Cefepime for Injection USP and Dextrose Injection USP Due to Visible Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- Barrel O’ Fun Snack Foods Co. Issues Allergy Alert and Recall of Safeway Snack Artist BBQ Potato Chips Due to Mislabeling and Undeclared Allergens
- From: U.S. Food & Drug Administration (FDA)
- Turkey Hill Dairy Issues Voluntary Recall of Chocolate Peanut Butter Cup Premium Ice Cream, Fudge Ripple Premium Ice Cream, and Moose Tracks Stuff’d Frozen Dairy Dessert
- From: U.S. Food & Drug Administration (FDA)
- Dräger issues an update on its voluntary recall of Fabius anesthesia machines
- From: U.S. Food & Drug Administration (FDA)
- HOSPIRA ISSUES A VOLUNTARY NATIONWIDE RECALL OF ONE LOT OF METOCLOPRAMIDE INJECTION, USP, AND TWO LOTS OF ONDANSETRON INJECTION, USP, DUE TO GLASS (GLASS STRANDS) PARTICULATES CAUSED BY GLASS SUPPLIER DEFECT
- From: U.S. Food & Drug Administration (FDA)
- OnTime Distribution Inc. Recalls PRAN brand Spice Powder TURMERIC Due To Excessive Levels of Lead
- From: U.S. Food & Drug Administration (FDA)
- Asia Cash & Carry Inc. Recalls PRAN Brand Spice Powder Turmeric Due to Elevated Levels of Lead
- From: U.S. Food & Drug Administration (FDA)
- B@B Trade Inc. Issues a Voluntary Recall of "Slim Fortune", "Lidiy", and "Slim Expert" weight loss Dietary Supplement
- From: U.S. Food & Drug Administration (FDA)
- H&H Medical Corporation Issues Nationwide Recall of Emergency Cricothyrotomy Kit
- From: U.S. Food & Drug Administration (FDA)
- ForeCYTE Breast Health Test; Mammary Aspiration Specimen Cytology Test (MASCT)
- From: U.S. Food & Drug Administration (FDA)
- Orange County Produce, LLC Recalls Bell Peppers Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Hospira Issues A Voluntary Nationwide Recall Of One Lot Of 1% Lidocaine HCL Injection Due To The Presence Of Dark Particulate
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Engström Ventilator, Aespire View, Aisys, And Avance Anesthesia Machines: Voluntary Field Corrective Action - Potential Safety Issue
- FDA MedWatch - Avance, Aisys And Avance CS2 Anesthesia Delivery Systems: Voluntary Field Corrective Action - Potential Safety Issue
- FDA MedWatch - Cefepime For Injection, USP And Dextrose Injection, USP By B. Braun Medical Inc.: Recall - Visible Particulate Matter
- FDA MedWatch - Inclusig (Ponatinib): Drug Safety Communication - Increased Reports Of Serious Blood Clots In Arteries And Veins
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - OxyElite Pro: Health Advisory - Acute Hepatitis Illness Cases Linked to Product Use
- FDA MedWatch - Fabius Anesthesia Machines: Recall - Did Not Pass High Voltage Test Portion Of Final Production Test
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Breast Health Test and the Mammary Aspiration Specimen Cytology Test (MASCT): Recall - Concerns With Instructions For Use, Promotional Claims and FDA Clearance
- FDA MedWatch - 1% Lidocaine HCL Injection By Hospira: Recall - Presence Of Dark Particulate
- FDA MedWatch - Emergency Cricothyrotomy Kit By H&H Medical Corporation: Recall - Defective Cuff Balloon On Endotracheal Airway
- FDA MedWatch - Metoclopramide Injection And Ondansetron Injection by Hospira: Recall - Glass Strand Particulates Caused By Glass Supplier Defect
- ¿Qué pasa cuando cierra el Gobierno?
- Cierre del Gobierno 2013
- FDA MedWatch - Carefusion Avea Ventilator: Recall - Underreporting Of Tidal Volume If Used In Conjunction With Neonatal Hotwire Flow Sensor
- CVM Updates - Notification of Industry of Impacts of the Shutdown
- From: U.S. Food & Drug Administration (FDA)
- Big Blue Fisheries, Llc Recalls All Smoked Products From All Lots, Various Sizes, in Vacuum Packaging Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Carefusion Provides Update On Voluntary Recall Of Avea® Ventilator
- From: U.S. Food & Drug Administration (FDA)
- Afikim Electric Vehicles Issues Nationwide Recall of Breeze C Scooter
- From: U.S. Food & Drug Administration (FDA)
- Haute Health, LLC Conducts Voluntary Nationwide Recall of All Lots Of Virilis Pro, PHUK And Prolifta Capsules Due To Undeclared Ingredients
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new drug to treat major depressive disorder
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Perjeta for neoadjuvant breast cancer treatment
- From: U.S. Food & Drug Administration (FDA)
- Mercado de Seguros Médicos: qué hacer si tiene Medicare
- FDA MedWatch - The Compounding Shop - UPDATE: Do Not Use Budesonide Solution
- FDA MedWatch - Tygacil (tigecycline): Drug Safety Communication - Increased Risk of Death
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Safeway Recalls Several Varieties of Angel Food Cake Due to Undeclared Soy and Milk Allergens
- From: U.S. Food & Drug Administration (FDA)
- ¿Soy elegible para inscribirme en el Mercado de Seguros Médicos?
- CVM Updates - FDA Issues Guidance on Color Additives Used in Food for Animals
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 25, 2013
- From: U.S. Food & Drug Administration (FDA)
- Nuevos beneficios para matrimonios del mismo sexo
- Mercado de Seguros Médicos y los hispanos
- Envíenos sus preguntas sobre cómo proteger el dinero
- FDA MedWatch - W.S. Badger Company Daily SPF 30 Kids & Baby Sunscreen Lotion: Recall - Microbial Contamination
- FDA awards seven grants to stimulate development of pediatric medical devices
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Arzerra (ofatumumab) and Rituxan (rituximab): Drug Safety Communication - New Boxed Warning, Recommendations to Decrease Risk of Hepatitis B Reactivation
- W.S. Badger Company Voluntarily Recalls Select Lots of Daily SPF 30 Kids & Baby Sunscreen Lotions Due to Microbial Contamination
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Proposes Revision to Annual Report on Antimicrobials for Food-Producing Animals
- From: U.S. Food & Drug Administration (FDA)
- Garden Fresh Foods, Inc. Expanded Recalls on Specific Packages of Products Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Specific Lots of P.F. Chang's Home Menu Pork and Leek Dumpling Frozen Appetizers Recalled Due to Undeclared Allergen
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Duragesic (fentanyl) Patches: Drug Safety Communication - Packaging Changes to Minimize Risk of Accidental Exposure
- FDA issues final guidance on mobile medical apps
- From: U.S. Food & Drug Administration (FDA)
- U.S. Marshals seize food products at two Virginia food companies
- From: U.S. Food & Drug Administration (FDA)
- Semifreddi's Announces Voluntary Recall of Almond Biscotti and Chocolate Dipped Almond Biscotti for Undeclared Milk and Soy
- From: U.S. Food & Drug Administration (FDA)
- FDA finalizes new system to identify medical devices
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Baxter Dual Luer Lock Caps: Class I Recall - Presence of Loose Particulate Matter Found In Packaging
- Baxter Initiates Voluntary Recall of Two Lots of Dual Luer Lock Caps
- From: U.S. Food & Drug Administration (FDA)
- Wegmans Food Markets Issues Allergy Alert on Undeclared Soy (Allergen) in Wegmans Apple Cinnamon Mini Muffins, 14 oz.
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 18, 2013
- From: U.S. Food & Drug Administration (FDA)
- Sea voluntario en su comunidad
- Conversemos sobre cómo cuidar su dinero
- Mes de la Herencia Hispana
- Federal judge approves consent decree against Shamrock Medical Solutions Group
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA to Hold Two Additional Public Meetings on Major FSMA Proposed Rules
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - HeartSine Technologies Samaritan 300/300P PAD Public Access Defibrillators: Recall - Power, Battery Issues
- HeartSine Technologies, Ltd. Issues Global Correction of Samaritan® 300/300P PAD
- From: U.S. Food & Drug Administration (FDA)
- Qué deben hacer los conductores cuando los para un policía
- ¿Cuánto costará la cobertura del Mercado de Seguros Médicos?
- FDA approves first generic capecitabine to treat colorectal and breast cancers
- From: U.S. Food & Drug Administration (FDA)
- FDA prohibits manufacture of FDA-regulated drugs from Ranbaxy’s Mohali, India, plant and issues import alert
- From: U.S. Food & Drug Administration (FDA)
- Dutch Valley Food Distributors, Inc. Announces a Voluntary Nationwide Recall of Honey Roasted Peanuts, for Undeclared Milk and Wheat
- From: U.S. Food & Drug Administration (FDA)
- Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.25% Bupivacaine HCL Injection, USP (2.5 MG/ML), 30 ML Single-Dose Vial and One Lot of 0.75% Bupivacaine HCL Injection, USP (7.5 MG/ML), 30 ML Single Dose Vial Due to Presence of Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- Bupivacaine HCL Injection 0.25% (2.5 MG/ML) and Bupivacaine HCL 0.75% (7.5 MG/ML), 30 ML Single-Dose Vials by Hospira, Inc.: Recall- Presence of Particulate Matter
- FDA MedWatch - August 2013 Safety Labeling Changes includes 34 products with revisions to Prescribing Information
- New medical device treats urinary symptoms related to enlarged prostate
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Creafuse Powder Grape and Creafuse Powder Fruit Punch: Recall - Contains DMAA
- GE Pharma, LLC Announces a Recall of Dietary Supplement Creafuse Powder Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Schwebel Baking Company Voluntarily Recalls Schwebel's Golden Rich Buns With Honey Due to Undeclared Eggs
- From: U.S. Food & Drug Administration (FDA)
- Infórmese acerca del asma
- FDA MedWatch - Leiter's Compounding Pharmacy: Recall - Concerns of Sterility Assurance
- Medical Device Safety and Recalls: Siemens MicroScan Synergies plus® and MicroScan® rapID/S plus Negative Panels
- From: U.S. Food & Drug Administration (FDA)
- Leiter's Compounding Pharmacy Issues Voluntary Nationwide Recall of Three Product Lots Due to Lack of Assurance of Sterility Concerns Related to its Independent Testing Vendor
- From: U.S. Food & Drug Administration (FDA)
- Talenti® Gelato & Sorbetto Issues an Allergy Alert for Undeclared Allergen (Almonds) in Talenti German Chocolate Cake Gelato Pints
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 11, 2013
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Guidance on Information Recommended for Animal Food Additive Petitions
- From: U.S. Food & Drug Administration (FDA)
- Bubbles Baking Co. Issues an Allergen Alert for Undeclared Milk and Soy in First Street Label Blueberry Muffins, 14 oz. 9 Trays/ Case and Blueberry Loaf, 16 oz. 12 Trays/Case
- From: U.S. Food & Drug Administration (FDA)
- Conmemoración del 11 de septiembre
- FDA MedWatch - Park Compounding Sterile Medication: Recall – Concerns of Sterility Assurance
- Park Compounding: Sterile Medication Recall – Concerns of Sterility Assurance at Testing Vendor
- From: U.S. Food & Drug Administration (FDA)
- New Safety Measures Announced for Extended-Release and Long-Acting Opioids
- From: U.S. Food & Drug Administration (FDA)
- FDA announces safety labeling changes and postmarket study requirements for extended-release and long-acting opioid analgesics
- From: U.S. Food & Drug Administration (FDA)
- The September 2013 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Draft Guidance for Industry Available
- From: U.S. Food & Drug Administration (FDA)
- Avella Specialty Pharmacy Issues Voluntary Nationwide Recall of Two Medications Due to Concerns of Sterility Assurance at Testing Vendor
- From: U.S. Food & Drug Administration (FDA)
- General Mills Announces Voluntary Recall of Limited Quantity of Refrigerated Pillsbury Cinnamon Rolls With Icing
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Avella Specialty Pharmacy Sterile Medications: Recall - Concerns Of Sterility Assurance At Testing Vendor
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Altaire Pharmaceuticals Carboxymethylcellulose Sodium 0.5 Percent Ophthalmic Solution Sold Under Wal-Mart, CVS, and Target Brands: Recall - Preservative May Not Be Effective Through Expiry
- FDA MedWatch - MOTRIN Infants Drops Original Berry Flavor 1/2 fl oz: Recall - Particles Identified
- FDA MedWatch - University Compounding Pharmacy Injection Products: Recall - Lack of Sterility Assurance
- Altaire Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of 9 Lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution Sold Under Several Brands Because the Preservative May Not Be Effective Through Expiry
- From: U.S. Food & Drug Administration (FDA)
- McNeil Consumer Healthcare Announces Voluntary Recall of Three Lots of Concentrated MOTRIN Infants Drops Original Berry Flavor 1/2 fl oz.
- From: U.S. Food & Drug Administration (FDA)
- Updated Press Release: GoPicnic Brands Announces Voluntary Recall of Limited Quantity Vegan Meals Due to Undeclared Milk Allergen
- From: U.S. Food & Drug Administration (FDA)
- University Compounding Pharmacy Initiates a Nationwide Voluntary Recall of Certain Pharmacy Products due to Lack of Assurance of Sterility Concerns
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Federal judge grants FDA request for consent decree with Idaho farm
- From: U.S. Food & Drug Administration (FDA)
- Federal judge grants FDA request for consent decree with Idaho farm
- From: U.S. Food & Drug Administration (FDA)
- Cains Foods Issues an Allergen Alert for Undeclared Milk and Egg in Olde Cape Cod Chipotle Ranch Dressing
- From: U.S. Food & Drug Administration (FDA)
- Medaus Pharmacy Initiates a Nationwide Recall of Certain Pharmacy Products due to Questions Surrounding an Independent Third Party’s Sterility Testing
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 04, 2013
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Medaus Pharmacy Sterile Compounded Products - Recall: Inability to Confirm Sterility
- Chobani, Inc. Voluntarily Recalls Greek Yogurt Because of Product Concerns
- From: U.S. Food & Drug Administration (FDA)
- Ayuda financiera para estudiantes
- Update of CVM's What's New - Hubbard Feeds Inc. Announces an Expanded Voluntary Recall of Hubbard Life Homestead FastGrow Poultry Feed in Indiana, Michigan and Illinois Due to Elevated Calcium
- From: U.S. Food & Drug Administration (FDA)
- Hubbard Feeds Inc. Announces an Expanded Voluntary Recall of Hubbard Life Homestead FastGrow Poultry Feed in Indiana, Michigan and Illinois Due to Elevated Calcium
- From: U.S. Food & Drug Administration (FDA)
- Mercado de Seguros Médicos para pequeños negocios
- FDA MedWatch - Siemens MicroScan Synergies Plus And MicroScan RapID/S Plus Negative Panels: Class I Recall - False Susceptible And False Intermediate Results
- Update of CVM's What's New - Animal Drug Approvals September 2013 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Siemens MicroScan Synergies plus® and MicroScan® rapID/S plus Negative Panels
- From: U.S. Food & Drug Administration (FDA)
- Back to School: Is your kid a flu fighter?
- 6 consejos para la seguridad de los jóvenes en las redes sociales
- Update of CVM's What's New - Global Animal Health Conference
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Nestlé Purina Voluntarily Recalls Limited Number of Purina ONE beyOnd Our White Meat Chicken & Whole Barley Recipe Adult Dry Dog Food Bags
- From: U.S. Food & Drug Administration (FDA)
- Garden-fresh Foods, Inc. Recalls Spartan Fresh Selection American Potato Salad in 16 Oz. Packages Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Hospira Issues A Voluntary Nationwide Recall Of One Lot Of Aminosyn II 10 percent, Sulfite-Free, Due To Foreign Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- Premier Foods, LLC Announces The Recall Of Products Sold At Williams-Sonoma For Undeclared Allergens
- From: U.S. Food & Drug Administration (FDA)
- Nestle Purina Voluntarily Recalls Limited Number of Purina ONE beyOnd Our White Meat Chicken and Whole Barley Recipe Adult Dry Dog Food Bags Due to a Potential Health Risk
- 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)
- Wellness Pharmacy, Inc. Issues Voluntary Recall of Six Medications Due to Concerns of Sterility Assurance at Testing Vendor
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Cubicin (daptomycin for injection): Recall - Glass Particulate Matter Present in Four Lots
- FDA MedWatch - Gilenya (fingolimod) - Drug Safety Communication: Investigating Rare Brain Infection
- FDA MedWatch - Stryker Spine: Class 1 Recall - OASYS Midline Occiput Plate
- Cubist Pharmaceuticals Issues Voluntary Nationwide Recall of Four Lots of Cubicin (Daptomycin for Injection) 500mg in 10ml Single Use Vials Due to Presence of Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Cutting-Edge, Essential Science on Display
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Stryker Spine - OASYS Midline Occiput Plate
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Amport Foods Issues Allergy Alert on Undeclared Peanuts Mislabeled as Milk Chocolate Raisins
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 28, 2013
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Animal Feed Safety System Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Goldenfeast® Inc. Recalls Bird Food Due to Possible Salmonella Contamination from Parsley
- From: U.S. Food & Drug Administration (FDA)
- Goldenfeast® Inc. Recalls Bird Food Due to Possible Salmonella Contamination from Parsley
- From: U.S. Food & Drug Administration (FDA)
- Wellness Pharmacy, Inc. Issues Nationwide Voluntary Recall of Certain Sterile Products due to Laboratory Results Indicating Microbial Contamination
- From: U.S. Food & Drug Administration (FDA)
- Hardmenstore.com Issues Voluntary Nationwide Recall of 72HP, Evil Root and Pro Power Max Due to Undeclared Sildenafil
- From: U.S. Food & Drug Administration (FDA)
- JCB Laboratories Issues Voluntary Recall of Six Drug Product Lots Due to Concerns of Sterility Assurance at Testing Vendor
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Wellness Pharmacy, Inc. Products: Recall - Laboratory Results Indicating Microbial Contamination
- FDA MedWatch - JCB Laboratories Products: Recall - Sterility Assurance at Testing Vendor
- FDA MedWatch -
- Park Pharmacy & Compounding Center is Issuing a Voluntary Recall of Two Compounded Sterile Preparations. The Recall is Due to a Lack of Sterility Assurance
- From: U.S. Food & Drug Administration (FDA)
- Dove Chocolate Discoveries Issues Allergy Alert on Undeclared Nuts in Dark Chocolate Covered Fruit Collection Box
- From: U.S. Food & Drug Administration (FDA)
- Product Recall of Kroger’s Break ‘n Bake Chocolate Chip Cookie Dough Due to Peanut Butter Cup Cookie Dough Mispacked Into Chocolate Chip Cookie Dough Packages
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- REACTION NUTRITION, LLC issues allergy alert on undeclared milk in LIVE CLINICAL 90 CAPS
- From: U.S. Food & Drug Administration (FDA)
- Diagnósticos de autismo en niños hispanos
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Ortiga: Public Notification - Contains Hidden Drug Ingredient
- Update of CVM's What's New - FSMA Public Meeting
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Announces Phibro Animal Health Requests Voluntary Withdraw of Application for Medicated Poultry Feed
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 21, 2013
- From: U.S. Food & Drug Administration (FDA)
- New test system identifies 193 different yeasts and bacteria known to cause illness
- From: U.S. Food & Drug Administration (FDA)
- Conozca más sobre el Mercado de Seguros Médicos
- Terri Lynn, Inc. Issues Allergy Alert on Possible Undeclared Peanuts in its Packages of Deluxe Mixed Nuts
- From: U.S. Food & Drug Administration (FDA)
- Jack Rabbit Inc. Conducts Voluntary Nationwide Recall of Lot 2510 of Jack Rabbit Dietary Supplement Due to undeclared ingredient
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Reopening of Comment Period: HIV-Focused Drug Development and HIV Cure Research
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Covidien Monoject Prefill Flush Syringes: Recall - Not Subjected To AutoClave Sterilization Process Or Mismatched Syringe Tip Cap, Syringe Label, Filled Volume And Wrapper
- Herbal Give Care LLC Issues Voluntary Nationwide Recall of Esbelder Man Capsules, Esbelder Fem Capsules, and Esbelder Siloutte Capsules Vitamin Supplements Due to Potential Health Risks
- From: U.S. Food & Drug Administration (FDA)
- Mercado de Seguros Médicos: esté listo
- Aidapak Services Llc Initiates Voluntary Recall of Selected Pharmaceuticals Repackaged by Aidapak Services Llc Due to Potential Incorrect Labeling Aidapak Shipped Affected Products to Four States Only: Washington, Oregon, California, and Arizona
- From: U.S. Food & Drug Administration (FDA)
- Buurma Farms, Inc. Recalls Fresh Cilantro Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Aidapak Services LLC, Selected Repackaged Pharmaceuticals by Aidapack: Recall - Potential Incorrect Labeling
- Voluntary Recall of Limited Lots of Maple Almond Butter Jars and Chocolate Hazelnut Butter Jars
- From: U.S. Food & Drug Administration (FDA)
- Recuerde usar el cinturón de seguridad
- FDA MedWatch - UPDATE All Sterile Drug Products Made and Distributed By NuVision Pharmacy Dallas Facility: Recall - Lack Of Sterility Assurance
- Cómo ayudar a los padres a prepararse para el regreso a clases
- FDA reminds health care providers not to use sterile products from NuVision Pharmacy
- From: U.S. Food & Drug Administration (FDA)
- ¿Están sus hijos al día con las vacunas?
- Whole Foods Market Recalls Sour Cherry and Blueberry Crostatas Due to Undeclared Allergen
- From: U.S. Food & Drug Administration (FDA)
- Clarification to News Release Issued on August 9th Specialty Compounding, LLC Issues Nationwide Voluntary Recall of All Lots of Unexpired Sterile Products Due to Reports of Adverse Events
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Fluoroquinolone Antibacterial Drugs: Drug Safety Communication- Risk for Possibly Permanent Nerve Damage
- RECALL: Dry pet food due to possible health risk
- Ayuda del Gobierno: conozca más
- Empiece el nuevo año escolar bien preparado
- Update of CVM's What's New: P&G Voluntarily Recalls Limited Quantity of Dry Pet Food Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- P&G Voluntarily Recalls Limited Quantity of Dry Pet Food Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 14, 2013
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Hospira Blood Sets: Recall - Instances Of Outer Wall Of Blood Bags Punctured With Piercing Pin
- HIV/AIDS Update - Tivicay (dolutegravir), a new drug to treat HIV-1 infection approved
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new drug to treat HIV infection
- From: U.S. Food & Drug Administration (FDA)
- La FDA aprueba nuevo medicamento para el tratamiento de la infección de VIH
- From: U.S. Food & Drug Administration (FDA)
- El Mercado de Seguros de Salud y sus opciones
- FDA awards contract to develop promising new technology to test radiation countermeasures
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Iradimed Corporation, MRidium 3860+ Infusion Systems equipped with MRidium 1145 Dose Error Reduction System (DERS) Drug Library Kit: Class I Recall - Potential for Incorrect Recommended Infusion Rate
- FDA announces nationwide voluntary recall of all products for sterile use from Specialty Compounding
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - July 2013 Safety Labeling Changes includes 34 products with revisions to Prescribing Information
- Update of CVM's What's New
- From: U.S. Food & Drug Administration (FDA)
- Specialty Compounding, LLC Issues Nationwide Voluntary Recall of All Lots of Unexpired Sterile Products Due to Reports of Adverse Events
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Specialty Compounding Sterile Products: FDA Alert - Bacterial Infections - Update
- FDA MedWatch - Specialty Compounding Sterile Products: FDA Alert - Bacterial Infections
- The August 2013 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Aivlosin Untitled Letter Available
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - First rapid diagnostic test to detect both HIV-1 antigen and HIV-1/2 antibodies approved
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Cordis Optease Retrievable Inferior Vena Cava (IVC) Filter: Recall - Labeling Correction
- FDA approves first rapid diagnostic test to detect both HIV-1 antigen and HIV-1/2 antibodies
- From: U.S. Food & Drug Administration (FDA)
- Gold Star Smoked Fish Corp. Issues an Alert on Listeria in Baltic Treasures, Norwegian Style Matjes, Marinella "Delicatessnaya", Jewish Style Matjes, Traditional Russian Matjes,and Rybacka Wies Matjes Brands of Herring Fillets in Oil
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 07, 2013
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - CareFusion Alaris PC unit (model 8015) with version 9.12 Keyboard Processor: Class I Recall - Potential Loss of Communication Between Main Processor and Keyboard
- Heeren Brothers Recalls Cantaloupe Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Health and Beyond LLC Issues Voluntary Nationwide Recall of Tranquility Product Due to Product Having Traces of Pharmaceutical Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Evershing International Trading Inc. Announces Recall of Ginger Candy
- From: U.S. Food & Drug Administration (FDA)
- CTV BEST GROUP Inc. Issues Voluntary Nationwide Recall of Dietary Supplements BEST SLIM 40 Pills LOT # 109400 EXP: Dec. 31, 2016 because of Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Zip International Group, LLC Recalls Baltic Sprats in Spicy Brine Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Lactancia materna: ¿por qué es importante?
- Alerta de viaje en Yemen
- Marketplace information that meets your needs
- From: Health Insurance Marketplace
- Update of CVM's What's New - Updated Resolved Drug Shortages
- 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 Current Drug Shortages
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - Arthritis Drug for Horses and Dogs Scheduled to Return to Market
- From: U.S. Food & Drug Administration (FDA)
- Trois Comtois Recalls Trois Comtois Morbier Cheese for Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Advertencia sobre grave sarpullido vinculado al consumo de paracetamol
- FDA MedWatch - Benztropine Mesylate Injection (Nexus Pharmaceuticals): Recall - Visible Particulate Matter
- Nexus Pharmaceuticals Inc. Issues Voluntary Nationwide Recall of Benztropine Mesylate Injection, USP 2 mg/2 mL (1 mg/mL), in 2 mL Single Dose Vials
- From: U.S. Food & Drug Administration (FDA)
- FDA defines “gluten-free” for food labeling
- From: U.S. Food & Drug Administration (FDA)
- Aproveche las compras libres de impuesto
- Update of CVM's What's New - Animal Drug Approvals August 2013 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - - FDA Announces FY 2014 Animal Drug User Fee Rates for ADUFA and AGDUFA
- From: U.S. Food & Drug Administration (FDA)
- Purity First Health Products, Inc. Issues Nationwide Recall of Specific Lots of Healthy Life Chemistry B-50, Multi-Mineral and Vitamin C Products: Due to a Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market recalls Trois Comtois Morbier cheese because of possible health risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for July 31, 2013
- From: U.S. Food & Drug Administration (FDA)
- Beacon Hill Pharmacy d/b/a Rxtra Solutions Issues Voluntary Nationwide Recall of Certain Sterile Products Due to a Question of Sterility Assurance
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Acetaminophen: Drug Safety Communication - Association with Risk of Serious Skin Reactions
- FDA MedWatch - DePuy Orthopaedics - LPS Lower Extremity Dovetail Intercalary Component: Class 1 Recall - Potential for Fracture of Device
- HIV/AIDS Update - Tentative approval of emtricitabine and tenofovir disoproxil fumarate tablets, 200 mg/300 mg
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Healthy Life Chemistry By Purity First B-50: FDA Health Risk Warning - Undeclared Ingredients UPDATE
- FDA MedWatch - Beacon Hill Medical Pharmacy/Rxtra Solutions: Recall - Lack of Sterility Assurance
- Update of CVM's What's New - FSMA Update
- From: U.S. Food & Drug Administration (FDA)
- Cómo preparar almuerzos saludables para niños
- FDA Veterinarian - August 1, 2013
- From: U.S. Food & Drug Administration (FDA)
- FDA announces a voluntary recall of Nova Max Blood Glucose Test Strips
- From: U.S. Food & Drug Administration (FDA)
- Lipari Foods Recalls Wholey Peeled Cooked Tail-on 31/40 Count Shrimp Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - GE Healthcare Nuclear Medicine Systems: Class I Recall - Serious Injuries or Deaths Could Occur
- Voluntary Recall of Specified Lots of Nova Max® Glucose Test Strips
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Nova Max Glucose Test Strips: Recall - May Report False, Abnormally High Blood Glucose Result
- FDA MedWatch - Mefloquine Hydrochloride: Drug Safety Communication - Label Changes Due To Risk of Serious Psychiatric and Nerve Side Effects
- Update of CVM's What's New - New Videos from CVM's International Programs Team
- From: U.S. Food & Drug Administration (FDA)
- FDA warns consumers about health risks with Healthy Life Chemistry dietary supplement
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Healthy Life Chemistry By Purity First B-50: FDA Health Risk Warning - Undeclared Ingredients
- Gold Star Smoked Fish Corp. Issues an Alert on Listeria in Rybacka Wies Brand Herring Fillets in Oil "Matjes Sledz w oleju"
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Strengthening Oversight of Imported Foods
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - changes to VIREAD (tenofovir DF) labeling for Hepatitis B
- From: U.S. Food & Drug Administration (FDA)
- FDA takes step to help ensure the safety of imported food
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Nizoral (ketoconazole): Drug Safety Communication - Potentially Fatal Liver Injury, Risk of Drug Interactions and Adrenal Gland Problems
- Zip International Group LLC Recalls Herring Fillet in Oil Due to Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA permits marketing of first U.S. test labeled for simultaneous detection of tuberculosis bacteria and resistance to the antibiotic rifampin
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for July 24, 2013
- From: U.S. Food & Drug Administration (FDA)
- Ferrara Candy Company Voluntarily Issues Allergy Alert on Undeclared Peanuts and Tree Nuts in Brach’s Malted Milk Balls
- From: U.S. Food & Drug Administration (FDA)
- Beware of Illegally Sold Diabetes Treatments
- From: FDA Office of Women's Health
- Olam Tomato Processors, Inc. Announces Voluntary Recall of Mild and Medium Chunky Salsa Because It May Contain Large Glass Pieces
- From: U.S. Food & Drug Administration (FDA)
- Esté al día con la información del Gobierno
- FDA MedWatch - LeMaitre Vascular, Inc., Albograft Vascular Graft: Class I Recall - Blood Leak
- Update of CVM's What's New: FDA Amends Regulations to Remove Requirement to Destroy Viable Turtle Eggs and Live Turtles
- From: U.S. Food & Drug Administration (FDA)
- Cuidado de animales durante un desastre
- FDA invites public input on menthol in cigarettes
- From: U.S. Food & Drug Administration (FDA)
- FDA alerts companies to stop illegal sale of treatments for diabetes
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Diabetes Treatments: FDA Alerts of Illegal Sales - Undeclared Ingredients
- FDA MedWatch - MedStream Programmable Infusion Pump: Class 1 Recall - Malfunction In The Fill Level Sensor
- Herbal Give Care LLC Issues Voluntary Nationwide Recall of Esbelin Siloutte Te and Esbelin Siloutte Vitamin Supplement Due to Potential Health Risks
- From: U.S. Food & Drug Administration (FDA)
- Mercado de Seguros de Salud y los hispanos
- FDA MedWatch - Bryan Medical Tracoe Mini 3.0mm Tracheostomy Tube: Class 1 Recall - Mislabeled Packaging
- Volcano Company, Issues Voluntary Worldwide/Nationwide Recall of Volcano Male Enhancement Liquid and Volcano Male Enhancement Capsules, Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Square Mile Cider Company Announces Voluntary Recall of 2,500 Cases of Hard Cider Products
- 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)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Additional access info for July 25 webinar
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - July 25 webinar on Draft Guidance: Human Immunodeficiency Virus-1 Infection: Developing Antiretroviral Drugs for Treatment
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for July 17, 2013
- From: U.S. Food & Drug Administration (FDA)
- Seguro Social: nuevo sitio móvil
- ¿Necesita un seguro médico ahora?
- Campamentos de verano: averigüe si es elegible para un crédito tributario
- Whole Foods Market’s Mid-Atlantic Region Recalls Pimiento Cheese Due to Undeclared Egg
- From: U.S. Food & Drug Administration (FDA)
- USCIS responde a sus preguntas sobre inmigración
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Hagee Foods Inc. dba Penny's Salsa Inc. Recalls Hummus Products Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Prevenga el cáncer de piel
- Cuatro motivos para visitar una biblioteca este verano
- Sugerencias del Gobierno para encontrar empleo
- Update of CVM's What's New - Global Animal Health Conference
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Compliance Policy Guide for Salmonella in Food for Animals
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- REVISED - Western Mixers Produce & Nuts, Inc. Recalls Pistachios Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA permits marketing of first brain wave test to help assess children and teens for ADHD
- From: U.S. Food & Drug Administration (FDA)
- Hardmenstore.com Issues Voluntary Nationwide Recall of Silver Sword and Clalis at the Request of the FDA
- From: U.S. Food & Drug Administration (FDA)
- Olde Thompson Inc. Issues a Voluntary Recall of Earth’s Pride Organics: Organic Oregano 2.2 Oz Glass Jars With Cork Closure Due to Possible Salmonella Risk
- From: U.S. Food & Drug Administration (FDA)
- Due to a Class I recall by ARO Pistachio, Torn and Glasser, Inc Announces Voluntary Recall of Pistachios Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- USCIS responde a sus preguntas sobre inmigración
- FDA permits marketing of quicker method for checking effectiveness of medical device steam sterilization
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Medtronic MiniMed Paradigm Insulin Infusion Sets: Class 1 Recall - Potential for Over or Under Delivery of Insulin
- Update of CVM's What's New - New Video Available - Medicated Feed Rules for Animal Feed Manufacturers
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - June 2013 Safety Labeling Changes includes 44 products with revisions to Prescribing Information
- FDA approves new treatment for a type of late-stage lung cancer
- From: U.S. Food & Drug Administration (FDA)
- Western Mixers Produce & Nuts, Inc. Recalls Pistachios Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Use los registros públicos de delicuentes sexuales
- U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications 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)
- ¿Quiere refinanciar su hipoteca?
- Enforcement Report for July 10, 2013
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Verathon, Inc., GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 Reusable Blades: Class I Recall - Risk of Blade Tip Breakage and Premature Failure
- Update of CVM's What's New - FDA, Justice Department takes action against Vermont dairy farm
- From: U.S. Food & Drug Administration (FDA)
- FDA, Justice Department takes action against Vermont dairy farm
- From: U.S. Food & Drug Administration (FDA)
- Use una carta de queja efectiva para presentar su reclamo
- Enforcement Report for July 03, 2013
- From: U.S. Food & Drug Administration (FDA)
- The July 2013 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New: Hubbard Feeds Inc. Announces Voluntary Recall in Indiana and Michigan Due to Potentially Elevated Calcium and Phosphorus in Medicated Poultry Feed
- From: U.S. Food & Drug Administration (FDA)
- Hubbard Feeds Inc. Announces Voluntary Recall in Indiana and Michigan Due to Potentially Elevated Calcium and Phosphorus in Medicated Poultry Feed
- From: U.S. Food & Drug Administration (FDA)
- Tormentas eléctricas: cómo protegerse
- FDA MedWatch - Estarylla (norgestimate and ethinyl estradiol): Recall - Report of Placebo Tablet Present in Row of Active Tablets
- Somersault Snack Co. Issues Allergy Alert On A Limited Number Of 1 Oz. Packages Of Somersault Pacific Sea Salt Distributed Solely To Target Stores In 6-count Multipacks
- From: U.S. Food & Drug Administration (FDA)
- Sandoz US Announces Voluntary Nationwide Recall of One Lot of Estarylla
- From: U.S. Food & Drug Administration (FDA)
- Crave Brothers Farmstead Cheese Recalls Les Freres Cheese Products
- From: U.S. Food & Drug Administration (FDA)
- Somersault Snack Co. Issues Allergy Alert on a Limited Number of 1 oz. Packages of Somersault Pacific Sea Salt Distributed Solely to Target Stores in 6-count Multipacks
- From: U.S. Food & Drug Administration (FDA)
- Celebramos el 4 de Julio y grandes inventos
- Celebramos el 4 de julio y grandes inventos
- Fuegos artificiales: consejos de seguridad
- HealthCare.gov: The Health Insurance Marketplace that Serves You
- From: Health Insurance Marketplace
- Celebramos el 4 de julio y grandes inventos: el Internet
- FDA MedWatch - Olmesartan Medoxomil: Drug Safety Communication - Label Changes To Include Intestinal Problems (Sprue-Like Enteropathy)
- Medicines in My Home Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - RECOMBIVAX HB (Hepatitis B Vaccine (Recombinant)) Adult Formulation by Merck Sharp and Dohme Corp.: Recall - Potential For Cracked Vials
- HEALTH Advises Consumers Not to Eat Certain Olives
- 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)
- Celebramos el 4 de Julio y grandes inventos: lo que ha dado de qué hablar
- Update of CVM's What's New - Letter to Veterinary Professionals – FACTREL
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Benztropine Mesylate Injection by Fresenius Kabi USA: Recall - Potential Presence Of Glass Particles
- Update of CVM's What's New - Animal Drug Approvals July 2013 Update
- From: U.S. Food & Drug Administration (FDA)
- Fresenius Kabi USA Issues Voluntary Nationwide Recall of Benztropine Mesylate Injection, USP 2 mg/2 mL (1 mg/mL), in 2 mL Single Dose Vials
- From: U.S. Food & Drug Administration (FDA)
- Celebramos el 4 de Julio y grandes inventos: sumersión a fondo
- Cómo reconocer y denunciar el maltrato de niños y ancianos
- Talenti Gelato Issues Allergy Alert For Undeclared Allergen (pecans) In Toasted Almond Gelato
- From: U.S. Food & Drug Administration (FDA)
- Harmony Chai Voluntary Recall of Concentrated Black Spiced Chai and Decaffeinated Rooibos Chai
- From: U.S. Food & Drug Administration (FDA)
- UPDATED RELEASE #3 UPC Code Clarification Townsend Farms, Inc. Expands Voluntary Limited Lot Recall of Frozen Organic Antioxidant Blend, 3 lb. Bag
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Medtronic SynchroMed Implantable Infusion System Devices: Class 1 Recalls - Feed Through Failure, Failure of Priming Bolus, and Catheter Occlusion
- Medtronic Issues Medical Device Notifications Regarding The Synchromed Implantable Infusion System
- From: U.S. Food & Drug Administration (FDA)
- FDA approves the first non-hormonal treatment for hot flashes associated with menopause
- From: U.S. Food & Drug Administration (FDA)
- RECALL: Frozen Organic Pomegranate Kernels Due to Hep A contamination
- Federal judge enters consent decree with Med Prep Consulting
- From: U.S. Food & Drug Administration (FDA)
- Dolphin Intertrade Corp
- From: U.S. Food & Drug Administration (FDA)
- Disfrute este verano con sus hijos
- FDA approves first recombinant coagulation factor IX that is specifically indicated for routine use in preventing bleeding episodes (prophylaxis)
- From: U.S. Food & Drug Administration (FDA)
- Respironics California, Inc. Recall of V60 Ventilator Designated Class I by FDA
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update -Tentative approval of efavirenz, lamivudine and tenofovir disoproxil fumarate tablets
- From: U.S. Food & Drug Administration (FDA)
- FDA takes action to protect consumers from dangerous medicines sold by illegal online pharmacies
- From: U.S. Food & Drug Administration (FDA)
- Scenic Fruit Company Recalls Woodstock Frozen Organic Pomegranate Kernels Due To Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for June 26, 2013
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Beneficios del Gobierno: búsqueda fácil y rápida
- CVM Updates - Availability of CVM Internal Terms for Use in Veterinary Adverse Event Reporting
- From: U.S. Food & Drug Administration (FDA)
- Prueba del VIH
- Price Chopper Voluntarily Recalls 3 Varieties of Burst Brand Cookies
- From: U.S. Food & Drug Administration (FDA)
- Welcome to the new HealthCare.gov
- From: Health Insurance Marketplace
- FDA announces first decisions on new tobacco products through the substantial equivalence pathway
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - New Video - Safe Medicated Feed for Animal Producers
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Hydroxyethyl Starch Solutions: FDA Safety Communication - Boxed Warning on Increased Mortality and Severe Renal Injury and Risk of Bleeding
- 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 - New Safe Feed Webpage
- From: U.S. Food & Drug Administration (FDA)
[Index of Archives]
[CDC News]
[NIH News]
[Epson Inkjet]
[Yosemite]
