FDA News
[Prev Page][Next Page]
- Update of CVM's What's New - Animal Drug Approvals August 2014 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Regeneca Worldwide, A Division Of Vivaceuticals, Inc Voluntarily Recalls RegenESlim Appetite Control Capsules Due To The Presence Of DMAA That May Pose Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Cubist Pharmaceuticals Issues Voluntary U.S. Recall Of Certain Lots Of CUBICIN (Daptomycin For Injection) 500 mg In 10 mL Single Use Vials Due To Presence Of Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 06, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Cubicin (daptomycin for injection) 500 mg in 10 mL Single Use Vials: Recall - Presence Of Particulate Matter
- FDA MedWatch - RegenESlim Appetite Control Capsules: Recall - Presence Of DMAA
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Orbactiv to treat skin infections
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Ortho Molecular Products Issues Allergy Alert On Undeclared Milk In Lifecore Chocolate And Lifecore Complete Chocolate
- From: U.S. Food & Drug Administration (FDA)
- Oasis Brands, Inc Recalls Quesito Casero 12oz Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Expression Injectable by Enhancement Medical: FDA Safety Communication - Adverse Events Associated with Unapproved Use As a Dermal Filler
- The August 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Adverse Events Associated with Use of Enhancement Medical's "Expression" Intranasal Splint as a Dermal Filler
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Recomendaciones para realizar una mudanza
- New England Greens, LLC dba Vibrant Health Recalls Green Vibrance and Rainbow Vibrance Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- CDPH Warns Consumers Not to Eat VR Green Farms Jarred Food Products Because of Botulism Risk
- From: U.S. Food & Drug Administration (FDA)
- Sunburst Superfoods Recalls Organic Raw Carob Powder Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Wawona Packing Co. Expands Its Voluntary Recall of Fresh, Whole Peaches, Plums, Nectarines, and Pluots Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA expands approval of drug to treat Pompe disease to patients of all ages; removes risk mitigation strategy requirements
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Jardiance to treat type 2 diabetes
- From: U.S. Food & Drug Administration (FDA)
- FDA Veterinarian - August 1, 2014
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Current Animal Food GRAS Notices Inventory
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Natural Grocers by Vitamin Cottage Issues Voluntary Recall For Various Chunks of Energy Products Because They Contain Organic Carob Powder From Ciranda, Inc., Which May Be Contaminated With Salmonella
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for July 30, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Striverdi Respimat to treat chronic obstructive pulmonary disease
- From: U.S. Food & Drug Administration (FDA)
- FDA takes steps to help ensure the reliability of certain diagnostic tests
- 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)
- CVM Updates - FDA Announces FY 2015 Animal Drug User Fee Rates for ADUFA and AGDUFA
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Draft Guidance for Industry on Cell-Based Products for Animal Use
- From: U.S. Food & Drug Administration (FDA)
- SW Wisc Dairy Goat Products Coop issues voluntary recall of Raw Goat Milk Mild Cheddar Cheese Lot Code 103-114 because of possible health risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Lidocaine HCI Injection, USP, 2 percent, by Hospira: Recall - Visible Particulates
- Hummingbird Wholesale Recalls Organic Raw Carob Powder for Possible Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- CONSUMER ALERT: UNDECLARED MILK IN Uprising brand Carrot Drink, Beet Drink and in Peanut Punch
- From: U.S. Food & Drug Administration (FDA)
- Starway Inc. Issues an Alert on Undeclared Sulfites in Peony Mark Brand Roasted and Salted Pumpkin Seeds
- From: U.S. Food & Drug Administration (FDA)
- Hospira Announces Voluntary Nationwide Recall Of One Lot Of Lidocaine HCI Injection, USP, 2 percent, 20 mg per mL Single-dose Vial, Preservative-free, Due To Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA Commissioner Margaret A. Hamburg’s Statement on the Surgeon General’s Call to Action to Prevent Skin Cancer
- From: U.S. Food & Drug Administration (FDA)
- CaCoCo, Inc. Recalls Raw Drinking Chocolate Containing Voluntarily Recalled Organic Carob Powder From Their Supplier for Possible Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- GOMACRO RECALLS "Almond Butter + Carob" and “Sunflower Butter + Chocolate” MacroBars Because of Possible Health Risk Carob Powder Supplier May Have Exposed Ingredient to Salmonella
- From: U.S. Food & Drug Administration (FDA)
- The TJX Companies, Inc. Recalls "Ecoato" Sweet Paprika Powder Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Carmel Food Group Announces a Voluntary Recall of One Code Date of Mislabeled Butternut Squash Ravioli Due to Undeclared Allergens
- From: U.S. Food & Drug Administration (FDA)
- FDA expands approved use of Imbruvica for chronic lymphocytic leukemia
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Provides Equine Veterinarians with Important Information about TILDREN and OSPHOS for Navicular Syndrome in Horses
- From: U.S. Food & Drug Administration (FDA)
- Dancing Star LLC, Buckland, MA 01338 Issues Voluntary Recall For Various Snacks Because They Contain Organic Carob Powder From Ciranda, Inc., Hudson, WI 54016, Which May Be Contaminated With Salmonella.
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: GE Healthcare, LLC, Single-Width Airway Modules (E-MiniC) and Accessories and Extension Modules (N-FC, N-FCREC) - CO2 Detector May Fail Leading to Injury
- From: U.S. Food & Drug Administration (FDA)
- GE Healthcare, LLC, Single-Width Airway Modules (E-MiniC) and Accessories and Extension Modules (N-FC, N-FCREC: Class I Recall - CO2 Detector May Fail Leading to Injury
- Texas Firm Recalls Ready-to-eat Products For Possible Listeria Contamination
- From: U.S. Food & Drug Administration (FDA)
- Lion Pavilion Issues Alert on Undeclared Sulfites in Tasty Peach Slices
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for July 23, 2014
- From: U.S. Food & Drug Administration (FDA)
- Earth Circle Organics Recalls Organic Carob Powder for Possible Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market Recalls Made-In-Store Items Prepared With Stone Fruit Voluntarily Recalled by Wawona Packing Co. Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new extended-release oxycodone with abuse-deterrent properties
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Zydelig for three types of blood cancers
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Ibuprofen and Oxcarbazepine Tablets by American Health Packaging: Recall - Mislabeled Packaging
- Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- American Health Packaging Announces the Voluntary Nationwide Recall of Ibuprofen Tablets, USP, 600 mg, 100 Hospital Unit Dose and Oxcarbazepine Tablets, 300 mg, 100 Hospital Unit Dose
- From: U.S. Food & Drug Administration (FDA)
- Unique Pharmaceuticals, Ltd. Announces a Voluntary Nationwide Recall of all Sterile Compounded Preparations Within Their Expiry Period Due to a Lack of Sterility Assurance
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market Hyannis Recalls Chocolate Chewies Cookies Due to Undeclared Tree Nut Allergen
- From: U.S. Food & Drug Administration (FDA)
- Wegmans Issues Voluntary Recall of Bakery Products That May Contain Fresh Peaches, Nectarines and Plums Supplied by Wawona Packing Company
- From: U.S. Food & Drug Administration (FDA)
- Wawona Packing Co. Takes Precautionary Step of Voluntarily Recalling Fresh, Whole Peaches, Plums, Nectarines, and Pluots Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Sterile Drug Products by Downing Labs (aka NuVision Pharmacy): Drug Alert - Lack of Sterility Assurance
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Take a new CME/CNE/CPE course on the Science of Sex and Gender in Human Health
- From: FDA Office of Women's Health
- Enforcement Report for July 16, 2014
- From: U.S. Food & Drug Administration (FDA)
- Mars Food North America Voluntarily Recalls Specific Batch and Item Number Representing Less Than 2,000 Cases
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- 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 approves new product to treat rare genetic disease
- From: U.S. Food & Drug Administration (FDA)
- Updated: Voluntary Nationwide Recall of Tattoo Ink, Tattoo Needles, Tattoo kits due to Microbial contamination
- From: U.S. Food & Drug Administration (FDA)
- Baxter Initiates Voluntary Worldwide Recall Of Four Lots Of IV Solutions Due To The Presence Of Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Consejos de seguridad para el verano
- King of Pops Charleston SC Issues Allergen Alert on Undeclared: Soy, Milk, Egg and Wheat
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - June 2014 Safety Labeling Changes includes 52 products with revisions to Prescribing Information
- 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)
- Voluntary Nationwide Recall of Tattoo Ink, Tattoo Needles, Tattoo kits Due to Microbial Contamination
- From: U.S. Food & Drug Administration (FDA)
- Sterile Drug Products by Unique Pharmaceuticals Ltd.: Recall - Lack of Sterility Assurance
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Hospira Lactated Ringer's And 5% Dextrose Injection, 1000 ML, Flexible Containers: Recall (One Lot) - Mold Contamination
- Hospira Issues Voluntary Nationwide Recall Of One Lot Of Lactated Ringers And 5% Dextrose Injection, Usp, 1000 Ml, Flexible Containers Due To Mold Contamination
- From: U.S. Food & Drug Administration (FDA)
- Charles Products Recalls Decorative Pint And Shot Glasses Due To Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for July 09, 2014
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Ventlab, LLC., Ventlab Manual Resuscitator, Duckbill Valve May Stick and Prevent Air from Getting to the Patient
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA to Hold Public Meeting on Antimicrobial Resistance Monitoring in the Food Supply
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market Recalls Pre-packaged Mini Caesar And Mini Mesclun Goat Cheese Salad In Three States, Due To Undeclared Allergen
- From: U.S. Food & Drug Administration (FDA)
- Vascular Solutions, Inc. Issues Recall of Langston Dual Lumen Catheters
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Langston V2 Dual Lumen Catheters (Models 5540 and 5550) by Vascular Solutions: Class I Recall - Inner Catheter May Separate During Use and Cause Injury
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA Classifies ConvaTec’s Voluntary Global Recall of Flexi-Seal™ CONTROL Fecal Management System (FMS) as Class I
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Vascular Solutions Langston V2 Dual Lumen Catheters (Models 5540 and 5550) - Inner Catheter May Separate During Use and Cause Injury
- 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)
- Huracán Arthur: esté preparado
- The July 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Beleodaq to treat rare, aggressive form of non-Hodgkin lymphoma
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for July 02, 2014
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Medtronic Neurosurgery, Medtronic Duet External Drainage and Monitoring System - Patient Line Tubing May Disconnect and Lead to Injury
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Medtronic Duet External Drainage and Monitoring System, Medtronic Neurosurgery: Class 1 Recall - Tubing May Disconnect and Lead to Injury
- Update of CVM's What's New - Cargill Conducts Voluntary Recall of Select Nutrena® NatureWise® Meatbird Feed
- From: U.S. Food & Drug Administration (FDA)
- Cargill Conducts Voluntary Recall of Select Nutrena® NatureWise® Meatbird Feed Due to Possible Animal Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Federal judge approves consent decree with New York dietary supplement maker
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals July 2014 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Oriya Organics, LLC Voluntarily Recalls Oriya Organics Superfood Protein Medley Containing Sprouted Chia Seed Powder for Possible Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- Mantenga su casa libre de plagas sin usar pesticidas
- FDA MedWatch - Coumadin (warfarin sodium) for Injection by Bristol-Myers Squibb: Recall - Particulate Matter
- FDA seeks permanent injunction against California pharmaceutical company
- From: U.S. Food & Drug Administration (FDA)
- Flowers Foods Issues Allergy Alert and Voluntary Recall on Limited Quantity of Sunbeam, Bunny, Flowers Deli, and Ingles Bar-B-Q Bread Sold in Alabama, Georgia, Louisiana, and Tennessee
- From: U.S. Food & Drug Administration (FDA)
- Bristol-Myers Squibb Issues Voluntary Nationwide Recall of COUMADIN (Warfarin Sodium) for Injection Due to Presence of Particulate Matter
- From: U.S. Food & Drug Administration (FDA)
- FDA outlines expectations for human drug compounders, including registered outsourcing facilities
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Medical Supply Liquidators Injectable Vitamin Products With a "Sunshine Labs" Label: Warning - Products Not FDA Approved
- CVM Updates - FDA Secures Full Industry Engagement on Antimicrobial Resistance Strategy
- From: U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update: OTC medicines and driving
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Afrezza to treat diabetes
- From: U.S. Food & Drug Administration (FDA)
- Health Matters America Inc. Of Cheektowaga, New York, Recalls Additional Sprouted Chia Seed And Sprouted Chia & Flax Seed Powder Due To Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for June 25, 2014
- From: U.S. Food & Drug Administration (FDA)
- Kentucky oncology practice and its manager plead guilty to purchasing and selling unapproved chemotherapy drugs
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Lidocaine Viscous: Drug Safety Communication - Boxed Warning Required - Should Not Be Used to Treat Teething Pain
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Draft Guidance on the Use of Nanotechnology in Food for Animals
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: HydroFinity Hydrophilic Guidewire
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Over-The-Counter Topical Acne Products: Drug Safety Communication - Rare But Serious Hypersensitivity Reactions
- Doctor’s Best Issues Voluntary Nationwide Recall of Red Yeast Rice due to Undeclared Lovastatin
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Olmesartan: Drug Safety Communication - FDA Review Finds Cardiovascular Risks for Diabetics Not Conclusive
- FDA issues guidance to support the responsible development of nanotechnology products
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Provides Important Information to Veterinarians about PACCAL VET-CA1 for Treating Cancer in Dogs
- From: U.S. Food & Drug Administration (FDA)
- New Article on Women in Medical Device Clinical Trials
- From: FDA Office of Women's Health
- Update of CVM's What's New - Updated Current Animal Food GRAS Notices Inventory - AGRN 000-015
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated - Safe Use of Flea and Tick Products in Pets
- From: U.S. Food & Drug Administration (FDA)
- Kraft Foods Group Voluntarily Recalls Small Quantity of Velveeta Original
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Big Sky Diagnostic Imaging, LLC in Butte, Montana: FDA Safety Communication - Mammography Problems
- Medical Device Safety and Recalls:
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Sivextro to treat skin infections
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - ConvaTec, Inc., Flexi-Seal CONTROL Fecal Management System Kit: Class I Recall - Not Cleared for Marketing
- Medical Device Safety and Recalls: ConvaTec, Inc., Flexi-Seal CONTROL Fecal Management System Kit - Not Cleared for Marketing
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Docetaxel: Drug Safety Communication - May Cause Symptoms of Alcohol Intoxication
- FDA MedWatch - HydroFinity Hydrophilic Guidewires by NDC/Covidien: Recall - Outer Jacket Damage
- CVM Updates - FDA Announces Minor Use/Minor Species (MUMS) Grant Program Request for Applications
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for June 18, 2014
- From: U.S. Food & Drug Administration (FDA)
- NDC Implements Voluntary Recall of the Hydrofinity™ Hydrophilic Guidewire
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Marcaine (Bupivacaine HCI Injection, USP), 0.5 percent, 30 ML, Single-Dose, Preservative-Free Vial: Recall - Visible Particulates
- Hospira Announces Voluntary Nationwide Recall of One Lot of 0.5% Marcaine™ (Bupivacaine HCI Injection, USP), 30 ML, Single-Dose, Preservative-Free Vial Due to Visible Particulates
- From: U.S. Food & Drug Administration (FDA)
- Vita Food Products Issues Voluntary Recall of 4oz Vita Classic Premium Sliced Smoked Atlantic Salmon Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Domega NY International Co Ltd Issues Allergy Alert On Undeclared Peanuts And Milk In Gong Xifacai Gift Chocolates
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA to Reopen Comment Period on Reportable Food Registry ANPR
- From: U.S. Food & Drug Administration (FDA)
- Wegmans Food Markets, Inc. Issues Allergy Alert on Undeclared Egg in Wegmans Cinnamon Raisin Buns, 12 oz.
- From: U.S. Food & Drug Administration (FDA)
- Schnucks Bakery Recalls Devil’s Food Cakes Topped With Undeclared Pecans
- From: U.S. Food & Drug Administration (FDA)
- Smith's Country Cheese, Inc. Voluntarily RECALLS Waxed Gouda Wheels BECAUSE OF POSSIBLE HEALTH RISK
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - May 2014 Safety Labeling Changes includes 37 products with revisions to Prescribing Information
- La Finquita Emite Una Alerta De Alergias Debido A Una Contaminacion Potencial De Mani O Cacahuate Y Frutos Secos En El Quesito Fresco Campesino
- From: U.S. Food & Drug Administration (FDA)
- ¿Vale la pena cambiar de celular con un nuevo contrato?
- FDA MedWatch - Captomer and Captomer-250 by Thorne Research: FDA Warning - Potential Health Risks
- FDA MedWatch - Smiths Medical Portex Low Dead Space Connector with Sideport, 3.5mm: Class I Recall- One Lot Mislabeled
- FDA approves Lymphoseek to help determine the extent of head and neck cancer in the body
- From: U.S. Food & Drug Administration (FDA)
- Fish Family Farm, Inc. Issues Allergy Alert On Milk Products And Cream Due To Potential Peanut And Tree Nut Contamination
- From: U.S. Food & Drug Administration (FDA)
- La Finquita Cheese Issues An Allergy Alert Due To Potential Peanut And Tree Nut Contamination In Fresh Farmers Cheese
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Smiths Medical - Portex Low Dead Space Connector with Sideport, 3.5mm
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for June 11, 2014
- From: U.S. Food & Drug Administration (FDA)
- Voluntary Product Recall: Wegmans Bagged Ice Due to Possible Metal Fragments - Sold in VA, MD, NJ, and some PA stores only
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Advocate Redi-Code+ Blood Glucose Test Strips by Diabetic Supply of Suncoast: Recall- Labeling Error
- Princess House, Inc. hace un retiro voluntario de los Platos pequeños Marissa color mandarina debido a niveles de cadmio y plomo
- From: U.S. Food & Drug Administration (FDA)
- Allergy Alert on Undeclared Milk in Dark Old Fashioned Sponge Candy
- From: U.S. Food & Drug Administration (FDA)
- FDA Office of Women's Health June e-Update
- From: FDA Office of Women's Health
- Diabetic Supply of Suncoast, Inc. issues a Nationwide Voluntary Recall of BMB-BA006A Advocate Redi-Code+ Blood Glucose Test Strips
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Meeting Minutes Available for the ADUFA III Conditional Approval Working Group
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Listings - Medicated Feed Mill Licenses and VFD Distributor Notifications
- From: U.S. Food & Drug Administration (FDA)
- Lansal, Inc. Voluntarily Recalls Egg White Salad With Chives Due To Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- The June 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Dole Packaged Foods Recalls Roasted Garlic Tomato Basil Soup in Texas Due to Undeclared Milk Allergen
- From: U.S. Food & Drug Administration (FDA)
- Olde Thompson Inc. Issues a Voluntary Recall of Kirkland Signature Coarse Ground Malabar Pepper 12.7 oz Plastic Jars Due to Possible Salmonella Risk
- From: U.S. Food & Drug Administration (FDA)
- Navitas Naturals Expands Voluntary Recall for Organic Sprouted Chia Powder Products
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Changes to the Complera (emtricitabine/rilpivirine/tenofovir dispoproxil fumarate) labeling
- From: U.S. Food & Drug Administration (FDA)
- FDA approves the first antihemophilic factor, Fc fusion protein for patients with Hemophilia A
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - New pediatric dosage form and label changes for Reyataz (atazanavir)
- From: U.S. Food & Drug Administration (FDA)
- GreenSmoothieGirl Issues Voluntary Recall for Organic Sprouted Chia Seed Powder Products Because of Possible Health Risk
- 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)
- Rite Aid Voluntarily Recalls 16 oz. Pints of Mint ‘N Chip Thrifty Ice Cream
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - PGG/HSC Feed Company LLC Issues Voluntary Recall of Champion Lamb Texturized Feed B30
- From: U.S. Food & Drug Administration (FDA)
- PGG/HSC Feed Company LLC Issues Voluntary Recall of Champion Lamb Texturized Feed B30, Lot-88022114M908840
- From: U.S. Food & Drug Administration (FDA)
- Ocean Spray Voluntarily Recalls Limited Quantity of 8-ounce Greek Yogurt Covered Craisins® Dried Cranberries Which May Contain Undeclared Peanuts
- From: U.S. Food & Drug Administration (FDA)
- Health Matters America, Inc, Recalls Organic Sprouted Chia Seed Powder and Sprouted Chia/flax Seed Powder Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for June 04, 2014
- From: U.S. Food & Drug Administration (FDA)
- Baptista’s Bakery Inc. Issues Voluntary Recall for LiveGfree Rosemary and Olive Oil Multiseed Snack Crackers
- From: U.S. Food & Drug Administration (FDA)
- Glutino Voluntarily Recalls Glutino Rosemary and Olive Oil Snack Crackers (4.25 oz. and 20 oz.) Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals June 2014 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Cómo prepararse para la temporada de huracanes
- Update of CVM's What's New - Hill’s Pet Nutrition, Inc. Voluntarily Recalls 62 Bags of “Science Diet® Adult Small & Toy Breed™” Dry Dog Food
- From: U.S. Food & Drug Administration (FDA)
- Hill’s Pet Nutrition, Inc. Voluntarily Recalls 62 Bags of “Science Diet® Adult Small & Toy Breed™” Dry Dog Food in California, Hawaii and Nevada Because of Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Approves First Oral Drug for Fleas and Ticks in Dogs with Three Month Duration
- From: U.S. Food & Drug Administration (FDA)
- Princess House, Inc. Voluntarily Recalls Marissa Tangerine Appetizer Plates Due to Cadmium and Lead Levels
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Soliris (eculizumab) Concentrated Solution for IV Infusion by Alexion: Recall - Visible Particulates
- Alexion Initiates Voluntary Nationwide Recall of Certain Lots of Soliris® (eculizumab) Concentrated Solution for Intravenous Infusion Due to the Presence of Visible Particulate Matter in a Single Lot
- From: U.S. Food & Drug Administration (FDA)
- FDA launches openFDA to provide easy access to valuable FDA public data
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Issues Final Compliance Policy Guide on Food Facility Registration
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - June 17 Workshop on HIV Cure Research
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first generic versions of celecoxib
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for May 28, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA allows marketing of first non-invasive test to help in identifying cause of certain kidney disease
- From: U.S. Food & Drug Administration (FDA)
- FDA to require warnings on sunlamp products
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Pet Center, Inc. Voluntary Recall of 3 oz bag of Lamb Crunchy’s Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Navitas Naturals Issues Voluntary Recall for Organic Sprouted Chia Seed Powder Products
- From: U.S. Food & Drug Administration (FDA)
- Eugene Oregon, Inc. Issues Voluntary Nationwide Expansion Of The Recall Of All Lots Of African Black Ant, Black Ant, And Mojo Risen Dietary Supplements Which May Contain Undeclared Active Pharmaceutical Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Fresenius NaturaLyte Liquid Bicarbonate Concentrate (Part Number: 08-4000-LB)
- From: U.S. Food & Drug Administration (FDA)
- Pet Center, Inc. Voluntary Recall of 3 oz bag of Lamb Crunchy’s Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Rome Packing Co., Inc. Recalls Minced Crab Meat Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- American Importing Co, Inc Issues Allergy Alert On Undeclared Almonds Mispacked As Cinnamon Crunch Granola
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Import Tolerance for teflubenzuron available
- From: U.S. Food & Drug Administration (FDA)
- Belleville Farmer’s Market Recalls Shelled Walnuts Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Sun Tree LLC Recalls 12oz Packaged California Grown Shelled Walnuts Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Brunkow Cheese Issues Allergy Alert On Undeclared Soy In Jalapeno Pepper Raw Milk Cheddar Cold Pack Cheese
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Product Shortage of Advanced Sterilization Products Sterrad Cyclesure 24 Biological Indicator
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Advanced Sterilization Products Sterrad Cyclesure 24 Biological Indicator: FDA Safety Communication - Product Shortage
- Medical Device Safety and Recalls: Fisher and Paykel Healthcare, Ltd., Infant Nasal CPAP Prongs
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Dalvance to treat skin infections
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market Recalls Thai Soba Noodle Salad in Five States, Due to Undeclared Allergen
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Fisher and Paykel Healthcare, Ltd., Infant Nasal CPAP Prongs: Class I Recall - Prongs May Detach from Nasal Tubing and Interrupt Therapy
- Kind Healthy Snacks Issues Allergy Alert Due to Potential Presence of Peanut Protein in Strong and Kind Bars and Kind Healthy Grains Maple Pumpkin Seeds Bars
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - NaturaLyte Liquid Bicarbonate Concentrate: Recall - Potential Health Risk
- FDA MedWatch - Baxter ABACUS TPN Calculation Software: Class I Recall - Software Errors May Cause Toxic/Overdose Symptoms
- FDA MedWatch - Maquet Datascope Intra-Aortic Balloon Pumps: Class I Recall - Failure of Fan Assembly
- Voluntary Nationwide and Canada Recall of NaturaLyte® Liquid Bicarbonate Concentrate Due to Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA targets illegal online pharmacies in globally coordinated action
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Baxter Corporation Englewood, ABACUS Total Parenteral Nutrition Calculation Software, Versions 3.1, 3.0, 2.1, and 2.0
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Maquet Datascope Corporation, Intra-Aortic Balloon Pumps, System 98/98XT, CS100/CS100i, and CS300
- From: U.S. Food & Drug Administration (FDA)
- Sherman Produce Recalls Bulk and Packaged Walnuts Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for May 21, 2014
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Investigates Outbreak of Human Salmonella Typhimurium Infections Linked to Frozen Feeder Rodents Packaged by Reptile Industries Inc.
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA is Vigilant About Keeping Your Pets Safe
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Alaris Pump Module (Model 8100), Version 9.1.18 Software by CareFusion 303, Inc: Class I Recall - May Not Properly Delay an Infusion
- Medical Device Safety and Recalls: CareFusion 303, Inc., Alaris Pump Module (Model 8100), Version 9.1.18 - Software May Not Properly Delay an Infusion with "Delay Until" Option or "Multidose" Feature
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FSMA - Extension of Comment Period for Proposed Rule on Sanitary Transportation of Human and Animal Food
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Get the Facts about Pain Relievers for Pets
- From: U.S. Food & Drug Administration (FDA)
- Middle East Bakery, Inc. Issues Allergy Alert on Undeclared Milk in Market Basket Dairy-free, Gluten-free Pancakes
- From: U.S. Food & Drug Administration (FDA)
- Lansal, Inc. Voluntarily Recalls Hummus & Dip Products Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Allergy Alert on Undeclared Milk in Pancakes
- From: U.S. Food & Drug Administration (FDA)
- Kraft Foods Group Voluntarily Recalls Select Cottage Cheese Products Due to Out-of-Standard Storage Temperatures
- From: U.S. Food & Drug Administration (FDA)
- WhiteWave Foods Issues Allergy Alert on Undeclared Almondmilk in Half Gallon Silk Light Original Soymilk Containers
- From: U.S. Food & Drug Administration (FDA)
- Áreas naturales para explorar en familia
- CVM Updates - FDA to Retain Current Small Numbers of Animals for Minor Use in Major Species
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Labetalol Hydrochloride Injection 100 MG/20 ML (5MG/ML), 20 ML, Multidose Vial by Hospira: Recall - Visible Particulates
- FDA MedWatch - Ventlab Resuscitator Bags: Recall - Possible Health Risk
- HIV/AIDS Update - Changes to the Trivicay (dolutegravir) product labeling
- From: U.S. Food & Drug Administration (FDA)
- Hospira Announces Voluntary Nationwide Recall Of One Lot Of Labetalol Hydrochloride Injection, USP, 100 MG/20 ML (5MG/ML), 20 ML, Multidose Vial, Due To Visable Particulates
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New
- From: U.S. Food & Drug Administration (FDA)
- Ventlab, LLC. Issues a Nationwide Recall of Ventlab Resuscitator Bags Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - April 2014 Drug Safety Labeling Changes includes 53 products with revisions to Prescribing Information
- CVM Updates - FDA Alerts Horse Owners and Veterinarians About Adverse Events Associated with Certain Unapproved Compounded Drugs in Horses
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Alere INRatio2 PT/INR Professional Test Strips - Results Disagree with the Confirmed PT/INR Reference Test Results Performed by Central Laboratory
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Eszopiclone Containing Sleep Aids: Drug Safety Communication - Can Cause Next-Day Impairment
- FDA MedWatch - Dobutamine Injection (250mg/20mL)/Hospira: Recall - Visible Particulates
- FDA requiring lower starting dose for sleep drug Lunesta
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Bravo® Issues Nationwide Recall of Pet Food for Dogs and Cats
- From: U.S. Food & Drug Administration (FDA)
- Bravo® Issues Nationwide Recall of Pet Food for Dogs and Cats
- From: U.S. Food & Drug Administration (FDA)
- Hospira Announces Voluntary Nationwide Recall Of One Lot Of Dobutamine Injection, USP, 250 MG, 20 ML, Single-Dose Fliptop Vial, Due To Visible Particulates
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for May 14, 2014
- From: U.S. Food & Drug Administration (FDA)
- US Trading Company Voluntary Recall of Crushed Chili Powder Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Pradaxa (dabigatran): Drug Safety Communication - Lower Risk for Stroke and Death, but Higher Risk for GI Bleeding Compared to Warfarin
- FDA Office of Women's Health - May e-Update
- From: FDA Office of Women's Health
- Surma Distributors LLC, Issues Alert On Undeclared Sulfites In Haque Brand Golden Raisins
- From: U.S. Food & Drug Administration (FDA)
- Domega Ny International Co Ltd Issues Allergy Alert On Undecleared Eggs In Brilliant Cake With Filling Milk (biscuits)
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Revised Guidance for Industry on Statistical Evaluation of Stability Data Available
- From: U.S. Food & Drug Administration (FDA)
- Strong America Limited ISSUES ALLERGY ALERT ON UNDECLARED EGG IN “Golden Smell Hotpot Meat Ball Medley”
- From: U.S. Food & Drug Administration (FDA)
- Stonyfield Extends Voluntary Recall of YoBaby Peach/Pear Yogurt Cup 6-packs to 271 Additional Stores in 6 Western States
- From: U.S. Food & Drug Administration (FDA)
- Domega NY International Co LTD Issues Allergy Alert On Undeclared Peanuts In YF Sesame Flavor Cracker
- From: U.S. Food & Drug Administration (FDA)
- Salud de la mujer: ¿tiene preguntas sobre su cobertura médica?
- Salud de la mujer: ¿tiene preguntas su cobertura médica?
- Datascope Corp/MAQUET Issues Worldwide Voluntary Recall of the System 98/98XT, CS100, CS100i and CS300 Intra-Aortic Balloon Pumps For Potential Mechanical Failure of the Power Supply Fan Assembly
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals May 2014 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Hospira Inc., GemStar Docking Station (List Number 13075) – Potential for Error or Failure to Power Up
- From: U.S. Food & Drug Administration (FDA)
- FDA allows marketing of first prosthetic arm that translates signals from person’s muscles to perform complex tasks
- From: U.S. Food & Drug Administration (FDA)
- STE Fromagere Du Livradois Voluntarily Recalls Raclette Cheese and Montboissie Cheese for Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Zontivity to reduce the risk of heart attacks and stroke in high-risk patients
- From: U.S. Food & Drug Administration (FDA)
- MDA Issues Consumer Advisory for Five Flavors of Lily Bloom’s Kitchen Poparoons Milk Ingredient was Undeclared on Labels
- From: U.S. Food & Drug Administration (FDA)
- Happy Mother's Day! Get FDA Resources for Moms
- From: FDA Office of Women's Health
- Update of CVM's What's New - How are we implementing the FSMA?
- From: U.S. Food & Drug Administration (FDA)
- The May 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for May 07, 2014
- 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)
- Medical Device Safety and Recalls: Safety Communication - Removing Retrievable Inferior Vena Cava Filters
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Alere INRatio2 PT/INR Professional Test Strips: Recall - Higher INR when Performed by Central Laboratory
- Alere Initiates Voluntary URGENT PRODUCT RECALL of Alere INRatio 2 PT/INR Professional Test Strips
- From: U.S. Food & Drug Administration (FDA)
- Pacific Organic Produce Announce Voluntary Recall of Mangos Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Eugene Oregon, Inc. Issues Voluntary Nationwide Recall of African Black Ant, Black Ant, and Mojo Risen Dietary Supplements Which May Contain Undeclared Active Pharmaceutical Ingredients
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Approves HALAMID Aqua to Treat Disease in Freshwater Fish
- From: U.S. Food & Drug Administration (FDA)
- Pacific Organic Produce Announce Voluntary Recall of Mangos Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Sixdog Investments Voluntarily Recalls Eggs Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Changes to the Edurant (rilpivirine) label: drug-drug interaction update
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Hospira Inc., Abbott Acclaim Infusion Pumps and Hospira Acclaim Encore Infusion Pumps - Broken Door Assemblies May Result in Over-Infusion or Delay of Therapy
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Listings - Approved Medicated Feed Mill Licenses/Veterinary Feed Directive Distributor Notifications
- From: U.S. Food & Drug Administration (FDA)
- Anhing Corporation Announces a Voluntary Recall of Chili Powder Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Blue Bunny Premium Bordeaux Cherry Chocolate Ice Cream Recalled for Undeclared Allergen
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Abbott Acclaim and Hospira Acclaim Encore Infusion Pumps by Hospira, Inc: Class I Recall - Broken Door Assemblies
- FDA MedWatch - Gemstar Docking Station by Hospira, Inc: Class I Recall - Potential for Error or Failure to Power Up
- Hospira Announces Urgent Nationwide Medical Device Correction For Gemstar Docking Station
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Sigma Spectrum Infusion Pumps with Master Drug Library by Baxter Healthcare: Class I Recall - System Error May Interrupt or Delay Therapy
- Update of CVM's What's New - Operational Strategy for Implementing the FDA Food Safety Modernization Act
- From: U.S. Food & Drug Administration (FDA)
- NOH Foods Of Hawaii Issues Allergy Alert On Undeclared Milk In Hawaiian Coconut Pudding Haupia (LUAU Dessert)
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for April 30, 2014
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update -Revised HHS Adult and Adolescent Antiretroviral Treatment Guidelines available
- From: U.S. Food & Drug Administration (FDA)
- Prevenga el maltrato infantil
- Medical Device Safety and Recalls: Baxter Healthcare Corporation, Sigma Spectrum Infusion Pumps with Master Drug Library Model No. 35700BAX and 35700ABB
- From: U.S. Food & Drug Administration (FDA)
- FDA Veterinarian - May 1, 2014
- From: U.S. Food & Drug Administration (FDA)
- Bacai Inc. Issues Voluntary Worldwide Recall of LiteFit USA
- From: U.S. Food & Drug Administration (FDA)
- Two Private Selection Ice Cream Flavors Recalled for Undeclared Allergen
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Flawless Beauty and Skin Products: Recall - Unapproved Drugs
- Flawless Beauty and Skin Issues Voluntary USA Recall of Unapproved Drugs
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Zykadia for late-stage lung cancer
- From: U.S. Food & Drug Administration (FDA)
- Resources for National Women’s Health Week
- From: FDA Office of Women's Health
- FDA MedWatch - GenStrip Blood Glucose Test Strips by Shasta Technologies: FDA Safety Communication - May Report False Results
- FDA MedWatch - HeartWare, Inc., Heartware Ventricular Assist System: Class I Recall - Locking Mechanism of Pump Driveline Connector May Fail to Engage
- Medical Device Safety and Recalls: HeartWare, Inc., Heartware Ventricular Assist System - Locking Mechanism of Pump Driveline Connector May Fail to Engage
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: FDA Safety Communication - Shasta Technologies GenStrip Blood Glucose Test Strips May Report False Results
- From: U.S. Food & Drug Administration (FDA)
- FDA issues proposals to address risks associated with surgical mesh for transvaginal repair of pelvic organ prolapse
- From: U.S. Food & Drug Administration (FDA)
- Medicines in My Home Update: Be Active in Your Health
- From: U.S. Food & Drug Administration (FDA)
- ¿Qué haría si pudiera regalarle a alguien más tiempo?
- FDA MedWatch - Super Arthgold by Nano Well-being Health: Recall - Undeclared Drug Ingredients
- Stonyfield Announces Voluntary Recall of 188 6-packs of Yobaby Peach/Pear Yogurt Cups from 40 Target Stores in the Southeast and 82 Mid-Atlantic Walmart Stores
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Questions and Answers for Brewers/Distillers on the FSMA Proposed Rule for Preventive Controls for Animal Food
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Voice - Getting it Right on Spent Grains
- 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 approves first human papillomavirus test for primary cervical cancer screening
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first human papillomavirus test for primary cervical cancer screening
- From: FDA Office of Women's Health
- FDA proposes to extend its tobacco authority to additional tobacco products, including e-cigarettes
- From: U.S. Food & Drug Administration (FDA)
- Nano Well-being Health Inc. Issues Voluntary Nationwide Recall of Super Arthgold Due to Undeclared Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Miravalle Foods, Inc. Recalls Ground Annato Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for April 23, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Sylvant for rare Castleman's disease
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Epidural Corticosteroid Injection: Drug Safety Communication - Risk of Rare But Serious Neurologic Problems
- Hospira Announces Voluntary Nationwide Recall of One Lot of 0.25% Marcaine™ (Bupivacaine HCI Injection, USP), 10 ml, Single-Dose, Preservative-Free Vial Due to Visible Particulates
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Marcaine (Bupivacaine HCI Injection, USP) 0.25 percent, 10 ml, Single-Dose, Preservative-Free Vial: Recall - Visible Particulates
- Hospira Announces Voluntary Nationwide Recall of One Lot of 0.25% Marcaine™ (Bupivacaine HCI Injection, USP), 10 ml, Single-Dose, Preservative-Free Vial Due to Visible Particulates
- From: U.S. Food & Drug Administration (FDA)
- Dominex Natural Foods, LLC, Issues Voluntary Recall Due to Possible Undeclared Nut Allergen in AngelBowls brand of Corkscrew Pasta & Creamy Tomato Vodka Sauce Pasta Bowl
- From: U.S. Food & Drug Administration (FDA)
- FDA proposes new expedited access program for medical devices that address unmet medical needs
- From: U.S. Food & Drug Administration (FDA)
- Wegmans Food Markets, Inc. Issues Allergy Alert on Undeclared Egg in Wegmans Easter Bread, 17 oz.
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Cyramza for stomach cancer
- From: U.S. Food & Drug Administration (FDA)
- Beneficios del Gobierno para personas con discapacidades
- Update of CVM's What's New - Updated Listing of Approved Medicated Feed Mill Licenses
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Covidien, Pipeline Embolization Device and Alligator Retrieval Device - (Certain Catalog / Lot Numbers) - Coating on Delivery Wire Could Delaminate and Detach
- From: U.S. Food & Drug Administration (FDA)
- Cómo obtener el estado de su reembolso de impuestos
- Hickory Farms Issues Allergy Alert on Chipotle Ranch Sauce Due to Undeclared Milk
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market Southwest Region Recalls Mini Butter Croissants Due to Undeclared Egg
- From: U.S. Food & Drug Administration (FDA)
- Hospira Announces Voluntary Nationwide Recall of One Lot of 1% Lidocaine HCI INjection, USP, Due To Visible Particulates
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Lidocaine HCI Injection, USP, by Hospira: Recall - Visible Particulates
- FDA MedWatch - CUBICIN (daptomycin for injection) by Cubist Pharmaceuticals: Recall - Presence of Particulate Matter
- FDA MedWatch - Propofol Injectable Emulsion, USP by Hospira: Recall - Visible Particulates
- Nature’s Universe Issues Voluntary Worldwide Recall of All Thinogenics Products Sold Prior to 02/06/2014 Due to the Presence of Undeclared Sibutramine
- From: U.S. Food & Drug Administration (FDA)
- Hospira Announces Nationwide Voluntary Recall of Seven Lots of Propofol Injectable Emulsion, USP, Due to Visible Particulates
- 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)
- Price Chopper Supermarkets Recalls Price Chopper Brand Tuscan White Bean Hummus due to Mislabeling
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Ragwitek for short ragweed pollen allergies
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Laparoscopic Power Morcellation in Hysterectomy and Myomectomy: FDA Safety Communication - Use Discouraged Due to Increased Risk in Women With Uterine Fibroids
- Medical Device Safety and Recalls: Spacelabs Healthcare Ltd., ARKON Anesthesia Delivery System with Version 2.0 Software - Software Defect May Cause System to Stop Working
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Laparoscopic Uterine Power Morcellation in Hysterectomy and Myomectomy - FDA Safety Communication
- From: U.S. Food & Drug Administration (FDA)
- Marsha Henderson Leads Programs to Improve Health Outcomes for Women
- From: FDA Office of Women's Health
- ¿Quiere refinanciar su hipoteca?
- FDA MedWatch - ARKON Anesthesia Delivery System with Version 2.0 Software by Spacelabs Healthcare: Class I Recall
- Update of CVM's What's New - New Brochure Available - Pet Turtles: A Source of Germs
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Purina Animal Nutrition LLC Recalls Poultry Feeds Due to Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Natural Organics, Inc. Recalls one lot ofTHURSDAY PLANTATION TEA TREE MOUTHWASH Due to Bacterial Contamination
- From: U.S. Food & Drug Administration (FDA)
- Health Matters America Inc. Issues Allergy Alert on Undeclared Milk in Organic Traditions Brand Dark Chocolate Golden Berries and Dark Chocolate Sacha Inchi Seeds
- From: U.S. Food & Drug Administration (FDA)
- Purina Animal Nutrition LLC Recalls Poultry Feeds Due to Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for April 16, 2014
- From: U.S. Food & Drug Administration (FDA)
- Cómo ahorrar y cuidar su dinero: publicaciones para usted
- Proteja a su bebé con las vacunas
- Update of CVM's What's New - Keep Lilies Away From Your Cats
- From: U.S. Food & Drug Administration (FDA)
- Private Selection Sweet Strawberry Sorbet Recalled for Undeclared Allergen
- From: U.S. Food & Drug Administration (FDA)
- La Compañía Fernández Chile Inc. retira del mercado Chile Molido Puro de 4 onzas y Chile Rojo de 6 onzas por contaminación potencial de Salmonella
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for April 09, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Covidien Pipeline Embolization Device and Alligator Retrieval Device: Recall - Coating on Delivery Wire Could Delaminate
- Covidien Implements Voluntary Recall of its Pipeline™ Embolization Device and Alligator™ Retrieval Device
- From: U.S. Food & Drug Administration (FDA)
- Sinco Inc Issues Allergy alert on undeclared Peanut Protein in Archer Farms Chocolate Hazelnut Swirl Gelato
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Abbott Diabetes Care, Inc. FreeStyle and FreeStyle Flash Blood Glucose Meters including the FreeStyle Blood Glucose Meter built into the OmniPod Personal Diabetes Manager (PDM)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - March 2014 Drug Safety Labeling Changes includes 30 products with revisions to Prescribing Information
- Fernandez Chile Company Inc. Recalls 4oz Chile Molido Puro and 6oz Chile Rojo Potential Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- FDA approves expanded indication for certain pacemakers and defibrillators
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Labeling update for Isentress (raltegravir)
- From: U.S. Food & Drug Administration (FDA)
- FDA Women's Health Highlights: April e-Update
- From: FDA Office of Women's Health
- Swanson Health Products Recalls Full Spectrum Cilantro
- From: U.S. Food & Drug Administration (FDA)
- Bissinger’s Announces a Voluntary Recall of Its Dark Chocolate Bunny Ears Due to Undeclared Milk
- From: U.S. Food & Drug Administration (FDA)
- Su declaración de impuestos: sugerencias para el último minuto
- Update of CVM's What's New - The Robert Abady Dog Food Co., LLC Recalls "Abady Highest Quality Maintenance & Growth Formula for Cats"
- From: U.S. Food & Drug Administration (FDA)
- Lisy Corporation Issues Recall on: Lisy Sweet Basil (Albahaca) 6 Oz., Item 1132 Lot #'s A013 0518 & A014 0518
- From: U.S. Food & Drug Administration (FDA)
- The Robert Abady Dog Food Co., LLC Recalls "Abady Highest Quality Maintenance & Growth Formula for Cats" Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Frontier Natural Products Co-op Initiates Voluntary Class 1 Recall Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Changes to the Prezista (darunavir) label
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Announces Voluntary Withdrawal of 19 Antimicrobials for Use in Food-Producing Animals
- From: U.S. Food & Drug Administration (FDA)
- Buffalo Sav Inc. Issues Allergy Alert On Undeclared Soy In “Grandma's Perogies Potato & Bacon Perogies”
- From: U.S. Food & Drug Administration (FDA)
- The April 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- OWH Director receives Women's Health Leadership Award
- From: FDA Office of Women's Health
- Update of CVM's What's New - Updated MUMS Drug Designations List/Veterinary Master Files
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Listing of Veterinary Feed Directive Distributor Notifications
- From: U.S. Food & Drug Administration (FDA)
- Frontier Natural Products Co-op Initiates Voluntary Class 1 Recall Due to Possible Health Risk from Organic Black Peppercorns
- From: U.S. Food & Drug Administration (FDA)
- Sprouts Farmers Market Recalls Organic Black Peppercorns Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market’s Northern California Region Recalls Chipotle Chicken Wraps Due to Undeclared Fish Allergen
- From: U.S. Food & Drug Administration (FDA)
- Publicaciones gratis para manejar mejor su dinero
- Asegure la educación de sus hijos con los planes 529
- U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
- From: U.S. Food & Drug Administration (FDA)
- Emparedados Boricua Emite Una Alerta Por Alérgenos En Sus Productos “Emparedados Boricua – Pollo y Queso”
- From: U.S. Food & Drug Administration (FDA)
- Koru Pacific Packaging Announces a Voluntary Recall for One Lot # AH!LASKA® Organic Cocoa Non-Dairy Chocolate Mix, 12 oz. Canister Due to Possible Milk Allergen
- From: U.S. Food & Drug Administration (FDA)
- Natural Organics, Inc. Recalls One Lot of THURSDAY PLANTATION TEA TREE MOUTHWASH Due to Bacterial Contamination
- From: U.S. Food & Drug Administration (FDA)
- Emparedados Boricua Issues Allergen Alert For Its Products "Emparedados Boricua - Chicken and Cheese"
- From: U.S. Food & Drug Administration (FDA)
- Proposed health IT strategy aims to promote innovation, protect patients, and avoid regulatory duplication
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Dräger Medical Inc., Evita V500 and Babylog VN500 Ventilators with Optional PS500 Power Supply Units - Battery Depletion
- From: U.S. Food & Drug Administration (FDA)
- FDA Commissioner Margaret A. Hamburg Statement on Prescription Opioid Abuse
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new hand-held auto-injector to reverse opioid overdose
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FSMA and Animal Feed - Final Rule and Guidance on Record Access Requirements
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for April 02, 2014
- From: U.S. Food & Drug Administration (FDA)
- Nuevos datos sobre el autismo revelan aumento en casos detectados
- FDA MedWatch - PS500 Power Supply Unit by Dräger: Recall - Early Depletion of Battery Charge
- Se vence el plazo para pagar los impuestos
- Dräger Issues Voluntary Nationwide Recall of Optional PS500 Power Supply for Evita V500 and Babylog VN500 Ventilators
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first sublingual allergen extract for the treatment of certain grass pollen allergies
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals April 2014 Update
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Thoratec Corporation, HeartMate II LVAS Pocket System Controller – Insufficient Labeling and Training for Patients Switched from the EPC Controller
- From: U.S. Food & Drug Administration (FDA)
- Lao Thai Nam Corp. Voluntarily Recalls Number One Sompa Salted Fish, Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Revatio (sildenafil): Drug Safety Communication - FDA Clarifies Warning About Pediatric Use for Pulmonary Arterial Hypertension
- Vita Food Products Issues Voluntary Recall of ELF Herring Fillets in Wine Sauce Containing Undeclared Milk
- From: U.S. Food & Drug Administration (FDA)
- Nova Products, Inc. Issues Voluntary Nationwide Recall of Dietary Supplements with Undeclared Active Pharmaceutical Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Fresh Express Issues Recall of Limited Quantity of Already Expired Italian Salad Due to Possible Health Risk, No Illnesses Cited
- From: U.S. Food & Drug Administration (FDA)
- FDA approves first long-acting recombinant coagulation Factor IX concentrate for patients with Hemophilia B
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Topamax for migraine prevention in adolescents
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Alli (60 mg orlistat capsules) by GlaxoSmithKline: Recall - Product Tampering
- Glaxosmithkline Recalls Alli®
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Announces Availability of Draft Guidance on Prior Notice of Imported Foods
- From: U.S. Food & Drug Administration (FDA)
- Macadamia Nut Allergy Alert and Voluntary Recall of 15-Count Boxes of Chocolate Chunk LUNA Bars Due to Package Mislabeling
- 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)
- BBM Chocolate Distributors, Ltd. Issues Allergy Alert on Undeclared Milk in "CHOCOLAT Alprose 52% CACAO PREMIUM DARK CHOCOLATE, Alprose Swiss Chocolate Dark Chocolate and CHOCOLAT Alprose NAPOLITAINS SWITZERLAND”
- From: U.S. Food & Drug Administration (FDA)
- Vermont Common Foods Issues Allergy Alert on Undeclared Peanuts
- From: U.S. Food & Drug Administration (FDA)
- Oscar’s Smokehouse, Inc. Recalls “Eleven Varieties (11) Of Cheese Spreads” Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for March 26, 2014
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Receives Strong Industry Commitment for its Antibiotic Resistance Strategy
- From: U.S. Food & Drug Administration (FDA)
- Pure Edge Nutrition, LLC Issues Voluntary Nationwide Recall of Bella Vi Brand Products Due to Undeclared Sibutramine and Phenolphthalein
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Partners With Veterinary Labs to Help Animals
- From: U.S. Food & Drug Administration (FDA)
- New Life Nutritional Center Issues Voluntary Nationwide Recall of Super Fat Burner, Maxi Gold and Esmeralda Dietary Supplements Due to the Presence of Undeclared Sibutramine and Phenolphthalein
- From: U.S. Food & Drug Administration (FDA)
- Parkers Farm Acquisition, LLC Issues Voluntary Recall of Products Due to Listeria Contamination
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Baraclude (entecavir) label revised to expand pediatric indication
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Otezla to treat psoriatic arthritis
- From: U.S. Food & Drug Administration (FDA)
- Helados La Tapatia, Inc. Retira Productos Debido a un Posible Riesgo de Salud
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Pleo Homeopathic Drug Products by Terra-Medica: Recall - Potential for Undeclared Penicillin
- FDA approves first implantable hearing device for adults with a certain kind of hearing loss
- From: U.S. Food & Drug Administration (FDA)
- Terra-Medica Issues Voluntary Nationwide Recall of Specified Lots of Pleo Homeopathic Drug Products Due to the Potential for Undeclared Penicillin
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Announces New Reporting Tool for Livestock Animal Food Problems
- From: U.S. Food & Drug Administration (FDA)
- Helados La Tapatia, Inc. Recalls Products Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for March 19, 2014
- From: U.S. Food & Drug Administration (FDA)
- Mercado de Seguros Médicos: cierre del plazo de inscripción
- FDA approves Impavido to treat tropical disease leishmaniasis
- From: U.S. Food & Drug Administration (FDA)
- Harry’s Farmers Market Recalls Amberjack From One Store in Marietta, GA. Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Update on Proposed Rules under the FDA Food Safety Modernization Act
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - February 2014 Drug Safety Labeling Changes includes 35 products with revisions to Prescribing Information
- Elija el mejor plan de seguro médico para usted y su familia
- March 21 Registration Deadline for Presenters at FDASIA 907 Public Hearing
- From: FDA Office of Women's Health
- CVM Updates - FDA Approves First Insulin Product for Use with Automatic Injection Pen in Cats and Dogs
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Playtex Nurser Deluxe Double Electric Breast Pump: Recall - Potential for Electric Shock
- Playtex Announces the Voluntary Nationwide Recall of Certain AC/DC Power Adapters Used With the Playtex® Nurser Deluxe Double Electric Breast Pump Due to Potential for Electric Shock
- From: U.S. Food & Drug Administration (FDA)
- Hospira Announces Voluntary Nationwide Recall of Hemoset Blood Set
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch -
- Cómo planificar un viaje en auto para toda la familia
- Fannie May Issues a Voluntary Recall of 89.08 Cases of 14.0 oz. Spring Wrapped Assorted Chocolate Box Due to Undeclared Peanuts
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Tentative approval of atazanavir sulfate and ritonavir Fixed-Dose Combination tablets
- From: U.S. Food & Drug Administration (FDA)
- Fannie May Issues A Voluntary Recall of 19 Boxes of 14.0 Oz. Spring Wrapped Assorted Chocolate Box Due to Undeclared Peanuts
- From: U.S. Food & Drug Administration (FDA)
- Simply Natural Foods, Llc Issues Allergy Alert For high Levels Of Milk Protein In Simply Lite Dark Chocolate Bars
- From: U.S. Food & Drug Administration (FDA)
- Some lots of Simply Lite brand dark chocolate recalled
- From: U.S. Food & Drug Administration (FDA)
- Infinite Herbs, LLC Voluntarily Recalls One Lot of Basil Organic Clamshells Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Tentative approval: lamivudine and tenofovir disoproxil fumarate FDC tablets with nevirapine
- From: U.S. Food & Drug Administration (FDA)
- Abbott Issues Recall of Certain Blood Glucose Monitoring Systems
- From: U.S. Food & Drug Administration (FDA)
- La Compania Pain Free by Nature Retira del Mercado las Tabletas de Reumofan Plus Debido a Ingredientes Medicos no Declarados
- From: U.S. Food & Drug Administration (FDA)
- SNI National is Voluntarily recalling Kratom XL 4 Pack, Maeng Da Kratom 10 Pack, Max Kratom 20 Pack, and Bali Kratom 40 pack Due to Undeclared Drug Ingredients
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - FreeStyle and FreeStyle Flash Blood Glucose Meter by Abbott: Recall - May Produce Mistakenly Low Blood Glucose Results
- Medical Device Safety and Recalls: McKesson Technologies, McKesson Anesthesia Care – Patient Case Data May Not Match Patient Data
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - VPRIV (velaglucerase alfa for injection): Recall - Visible Particulate Matter
- FDA MedWatch - Merit Medical Systems, Custom Procedural Trays/Kits Containing 1 percent Lidocaine HCl Injection, 10mg/mL: Recall - Particulates Found in Hospira supplied Lidocaine
- FDA MedWatch - Reumofan Plus: Recall - Undeclared Drug Ingredient [UPDATE]
- La Compania Pain Free by Nature Retira del Mercado las Tabletas de Reumofan Plus Debido a Ingredientes Medicos no Declarados
- From: U.S. Food & Drug Administration (FDA)
- Shire Pharmaceuticals Initiates Voluntary Nationwide Recall of One Batch, Packaged into Three Lots, of VPRIV® (velaglucerase alfa for injection)
- From: U.S. Food & Drug Administration (FDA)
- Dole Fresh Vegetables Voluntarily Recalls Limited Number of Bagged Salads Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Amends Regulations for Disclosure of New Animal Drug Approvals to Improve Timeliness of Public Disclosure
- From: U.S. Food & Drug Administration (FDA)
- Kirkland Signature Real Sliced Fruit Recalled Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- ¿Ya presentó su declaración de impuestos?
- Medical Device Safety and Recalls: Merit Medical Systems, Custom Procedural Trays/Kits Containing 1% Lidocaine HCl Injection, USP, 10mg/mL - Particulates Found in Hospira supplied 1% Lidocaine HCl
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Greatbatch Medical, Offset Cup Impactor - Inadequate Sterilization
- From: U.S. Food & Drug Administration (FDA)
- Pain Free by Nature is Voluntarily Recalling Reumofan Plus Tablets Due to Undeclared Drug Ingredients
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for March 12, 2014
- 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)
- 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 - 9 de marzo
- The March 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Philips Respironics, Trilogy Ventilator, Models 100, 200, and 202 - Failure to Deliver Mechanical Breaths
- From: U.S. Food & Drug Administration (FDA)
- Hong Lee Trading Inc. Issues an Alert on Undeclared Sulfites in “Mut Dua Non” Young Coconut Candy (Strips)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Effexor XR 150 Mg Extended-Release Capsules (Pfizer) and Venlafaxine HCl 150 Mg Extended-Release Capsules (Greenstone): Recall - Possible Presence of Tikosyn Capsules
- Net Food Brand Turkey Dried Apricots Recalled Because of Undeclared Sulfites
- From: U.S. Food & Drug Administration (FDA)
- Pfizer Initiates Nationwide Voluntary Recall of Two Lots of Pfizer’s Effexor XR® 150 Mg Extended-Release Capsules and One Lot of Greenstone’s Venlafaxine HCl 150 Mg Extended-Release Capsules Due to the Possible Presence of Tikosyn® Capsules
- From: U.S. Food & Drug Administration (FDA)
- Crown Food Distributors, Inc. Issues Allergy Alert on Undeclared Sulfites and Undeclared Yellow #6 in Golden Natural Fruit Island
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for March 05, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Doribax (doripenem): Drug Safety Communication - Risk When Used to Treat Pneumonia on Ventilated Patients
- FDA MedWatch - DIANEAL PD-2 Peritoneal Dialysis Solution with 1.5 Percent Dextrose 6000mL: Recall - Contamination With Mold
- FDA Office of Women's Health March e-Update
- From: FDA Office of Women's Health
- Gretchen’s Shoebox Express Issues Allergy Alert for Limited Number of Greek Yogurt Raspberry & Lemon Parfait cups Due to Undeclared Eggs.
- From: U.S. Food & Drug Administration (FDA)
- Baxter Initiates U.S. Voluntary Recall of One Lot of Peritoneal Dialysis Solution Due to Container-Closure Non-Integrity
- From: U.S. Food & Drug Administration (FDA)
- House of Flavors Issues Voluntary Recall Due to Possible Undeclared Nut Allergen in Belmont Chocolate Chip Cookie Dough Ice Cream
- From: U.S. Food & Drug Administration (FDA)
- Acceda a servicios del Gobierno
- Plum Organics Voluntarily Recalls Limited Quantity of Two Varieties of World Baby Pouch Products
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - HeartMate II LVAS Pocket System Controller by Thoratec Corporation: Medical Device Correction - Updated Labeling and Training Materials
- Twin Marquis, Inc Issues Allergy Alert on Undeclared Milk in Specific Lots of its Cooked Noodle and Lo Mein Noodle
- From: U.S. Food & Drug Administration (FDA)
- Thoratec Corporation Issues Worldwide Urgent Medical Device Correction Letter to Update its Labeling Regarding the Use of the HeartMate II® LVAS Pocket System Controller
- From: U.S. Food & Drug Administration (FDA)
- Lehigh Valley Dairy Conducts Voluntary Recall of Lehigh Valley, Swiss Premium, and Price Chopper Brand Orange Juice Because It May Contain Undeclared Allergen (Milk)
- From: U.S. Food & Drug Administration (FDA)
- ACTUALIZACIÓN (RETIRO EXTENDIDO) La compañía Roos Foods retira del mercado voluntariamente una variedad de quesos (enlistados abajo) debido a un posible riesgo sanitario
- From: U.S. Food & Drug Administration (FDA)
- HC Schau and Sons issues allergy alert on undeclared Pine Nuts in ‘Fresh To Go’ Tuscan Style Combo on Tomato Basil Bread (sandwich).
- From: U.S. Food & Drug Administration (FDA)
- Plum Organics Voluntarily Recalls Limited Quanity of Two Varieties of World Baby Pouch Products
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals March 2014 Update (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Conozca la diferencia entre la validez de su visa y el tiempo de estadía autorizado
- Usted y la Semana Nacional de Protección del Consumidor
- Unilever United States, Inc. Issues Allergy Alert for Limited Number of 20-Count Boxes of Popsicle Orange, Cherry and Grape Ice Pops Due to Undeclared Milk
- From: U.S. Food & Drug Administration (FDA)
- Jinsunmi International Inc. Issues A Voluntary Recall Of Its 17.98 oz Lotte Brand Frozen Fruit Bar (watermelon flavor) Due To Undeclared Peanuts
- From: U.S. Food & Drug Administration (FDA)
- Mars Food North America Voluntarily Recalls Specific Batch and Item Number Representing Less Than 3,500 Cases
- From: U.S. Food & Drug Administration (FDA)
- (UPDATE) EXPANDED - Roos Foods Voluntarily Recalls Variety of Cheeses (listed below) Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Resuscitation Systems with Oxygen and Air inlet Fittings Reversed During Assembly
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - GE Healthcare Resuscitation Systems: Class I Recall - Oxygen and Air Inlet Fittings Reversed During Assembly
- Update of CVM's What's New - CVM Feed Sampling Survey Assignments
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Announces New Program for State Animal Feed Regulators
- From: U.S. Food & Drug Administration (FDA)
- GobiernoUSA.gov en Twitter
- FDA proposes updates to Nutrition Facts label on food packages
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for February 26, 2014
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Tentative approval of emtricitabine and tenofovir disoproxil fumarate tablets, 200 mg/300 mg
- From: U.S. Food & Drug Administration (FDA)
- Investigan quesos contaminados de gran consumo hispano
- Medicines in My Home Update - American Heart Month reminder: Ask your doctor before taking daily aspirin
- From: U.S. Food & Drug Administration (FDA)
- Haga sus trámites fácilmente y en español
- Update of CVM's What's New - Paperwork Reduction Act Notices webpage available
- From: U.S. Food & Drug Administration (FDA)
- EXPANDIDO - La Compania Roos Foods Retira del Mercado Voluntariamente una Variedad de Quesos (Enlistados Abajo) Debido a un Posible Riesgo Sanitario
- From: U.S. Food & Drug Administration (FDA)
- EXPANDED - Roos Foods Voluntarily Recalls Variety of Cheeses (listed below) Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Changes to the Victrelis (boceprevir) label
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - ACME Monaco Guidewire .035x150 3MMJ TCFC, Item 88241 by Medline Industries: Class I Recall - Potential for Coating to Flake Off
- Medical Device Safety and Recalls: Medline Industries – ACME Monaco Guidewire .035x150 3MMJ TCFC, Item 88241
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - New Video Available - Pet Food and Treats in Your Home
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Myalept to treat rare metabolic disease
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Teleflex Medical, ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port - Potential Kinking During Patient Use
- From: U.S. Food & Drug Administration (FDA)
- La Compania Roos Foods Retira del Mercado Voluntariamente Una Variedad de Quesos (Enlistados Abajo) Debido a un Posible Riesgo Sanitario
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port (with and without Preloaded Stylet) by Teleflex Medical – Class I Recall: Potential Kinking During Patient Use
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- Wolfgang B. Gourmet Foods, Inc. Issues Allergy Alert on Undeclared Fish (Anchovies) in Two Lots Of Fairway Brand Condiment Grilling Sauce
- From: U.S. Food & Drug Administration (FDA)
- Roos Foods Voluntarily Recalls Variety of Cheeses Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Evolution Fresh Voluntarily Recalls Select Bottles of “Organic Sweet Greens and Ginger” Juice Sold at California and Nevada Grocery Retailers
- From: U.S. Food & Drug Administration (FDA)
- FDA issues first orders to stop sale, distribution of tobacco products
- From: U.S. Food & Drug Administration (FDA)
- Updated - Fannie May Issues A Voluntary Recall Of Its 4.0 Oz. Heart-shaped Box Of Assorted Chocolates Due To Undeclared Peanuts
- From: U.S. Food & Drug Administration (FDA)
- Falafel King Voluntarily Recalls Hatch Green Chile Hummus and Hatch Green Chile Wraps Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for February 19, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Etomidate Injection/Pfizer-Mylan: Recall - Presence of Particulate Matter and/or Illegible and Missing Lot Number and/or Expiry Date
- Update of CVM's What's New - Med-Vet International Issues Nationwide Recall of Veterinary 1/2cc U-40 Insulin Syringes Due to Mismarked Syringe Barrels
- From: U.S. Food & Drug Administration (FDA)
- Med-Vet International Issues Nationwide Recall of Veterinary 1/2cc U-40 Insulin Syringes Due to Mismarked Syringe Barrels
- From: U.S. Food & Drug Administration (FDA)
- Whole Foods Market Mid-Atlantic Region Recalls Tom Yom Soup Due to Undeclared Milk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Trilogy Ventilator Models 100, 200 and 202 by Philips Respironics: Recall - Failure to Deliver Mechanical Breaths
- Fannie May Issues A Voluntary Recall Of Its 4.0 Oz. Heart-shaped Box Of Assorted Chocolates Due To Undeclared Peanuts
- From: U.S. Food & Drug Administration (FDA)
- Agila Specialties Private Limited Initiates Voluntary Nationwide Recall of 10 Lots of Etomidate Injection 2 mg/mL – 10 mL and 20 mL due to the Presence of Particulate Matter and/or Illegible and Missing Lot Number and/or Expiry Date
- From: U.S. Food & Drug Administration (FDA)
- Philips Respironics Initiates Recall of Trilogy Ventilator
- From: U.S. Food & Drug Administration (FDA)
- FDA and European Medicines Agency strengthen collaboration in pharmacovigilance area
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Northera to treat neurogenic orthostatic hypotension
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Seeking Public Input on Animal Generic Drug User Fee Act Information Collection
- From: U.S. Food & Drug Administration (FDA)
- 3 temas populares sobre la jubilación
- Update of CVM's What's New - 2014 Windows to Regulatory Research Internship Program – Now Accepting Applications
- From: U.S. Food & Drug Administration (FDA)
- Ice Cream Specialties Issues Allergy Alert On Undeclared Peanut Allergen In Dairy Rich Chocolate Ice Cream
- From: U.S. Food & Drug Administration (FDA)
- MyNicKnaxs, LLC. Issues a Voluntary Nationwide and International Recall of All weight loss formulas of: Magic Slim, Fruta Bio, SlimEasy, Super Fat Burning Bomb, Slim Xtreme, Meizi Evolution, Meizitang Strong Version Botanical Slimming, Jianfeijindan Activity Girl, and Japan Hokkaido Cangye Phamacy Co., LTD Japanese Chinese Formula pill for weight reduction.
- From: U.S. Food & Drug Administration (FDA)
- Ben Venue Laboratories, Inc. Issues A Voluntary Nationwide Patient Level Recall Of Acetylcysteine Solution 10%, Usp, Lot 2005479
- From: U.S. Food & Drug Administration (FDA)
- Kettle Brand Voluntarily Recalls Limited Run of Bakes Sea Salt Potato Chips Due to Potential Milk Allergen
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for February 12, 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Acetylcysteine Solution 10 Percent: Recall - Glass Particles in Product
- FDA MedWatch - L-citrulline by Medisca: UPDATE - Additional Lot Numbers Recalled
- Su corazón es lo primero este día de San Valentín
- FDA MedWatch - L-citrulline by Medisca: Alert - Potentially Subpotent Product
- MyNicKnaxs, LLC. Issues a Voluntary Nationwide and International Recall of All Weight Loss Formulas of Reduce Weight Fruta Planta
- From: U.S. Food & Drug Administration (FDA)
- Illegal prescription drug sellers arraigned on charges for smuggling illicit cancer drugs into the United States
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FSMA Public Meeting: Proposed Rule on Sanitary Transportation of Human and Animal Food
- From: U.S. Food & Drug Administration (FDA)
- Tandem Diabetes Care Expands Voluntary Recall for Select Lots of Insulin Cartridges Used with t:slim Insulin Pump
- From: U.S. Food & Drug Administration (FDA)
- Roth Farms Recalls "Curly Parsley" Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Label update for Victrelis (boceprevir)
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Imbruvica to treat chronic lymphocytic leukemia
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - January 2014 Drug Safety Labeling Changes includes 23 products with revisions to Prescribing Information
- Mars Foodservices US Recalls Infused Rice Products Sold For Wholesale Distribution --UNCLE BEN’S® Retail Grocery Products Not Affected--
- From: U.S. Food & Drug Administration (FDA)
- FDA warns against using Uncle Ben’s Infused Rice
- From: U.S. Food & Drug Administration (FDA)
- Big Red Tomato Packers, LLC Voluntarily Recalls Fresh Tomatoes Due to Possible Risk of Contamination from Salmonella
- From: U.S. Food & Drug Administration (FDA)
- Natural Grocers by Vitamin Cottage Issues Allergy Alert on Undeclared Peanuts in Dark Chocolate Almonds
- From: U.S. Food & Drug Administration (FDA)
- The February 2014 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- FDA Office of Women's Health February e-Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Calcium gluconate 10 percent Injections by Rx Formulations: Recall - Microbial Contamination
- Update of CVM's What's New - FY 2013 ADUFA/AGDUFA Performance Reports Available
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Medicated Feed Mill Licenses/Veterinary Feed Directive Distributor Notications
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for February 05, 2014
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Pro-Pet LLC Recalls a Limited Number of Dry Dog and Cat Foods Due to Possible Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- Pro-Pet LLC Recalls a Limited Number of Dry Dog and Cat Foods Due to Possible Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- FDA Commissioner Hamburg travels to India
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - 2014 Windows to Regulatory Research Internship Program
- From: U.S. Food & Drug Administration (FDA)
- K-Fat Inc. Issues an Alert on Undeclared Sulfites In Kfi Sweetened Ginger Cand
- From: U.S. Food & Drug Administration (FDA)
- Humei Trading Inc. Issues Alert on Undeclared Sulfites in "Dried Lily"
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Animal Drug Approvals February 2014 Update
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update -Approval of generic version of lamivudine and zidovudine tablets, 150 mg/300 mg
- From: U.S. Food & Drug Administration (FDA)
- Cuide su corazón
- HIV/AIDS Update -Tentative approval of atazanavir sulfate capsules, 100 mg, 150 mg, 200 mg, and 300 mg
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Update to Food Safety Modernization Act and Animal Feed
- From: U.S. Food & Drug Administration (FDA)
- FDA Veterinarian - February 3, 2014
- From: U.S. Food & Drug Administration (FDA)
- UPDATE: Unified Grocers, Inc. Issues Allergy Alert on Undeclared Eggs in “Special Value Ginger Snap Cookies”
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Testosterone Products: Drug Safety Communication - FDA Investigating Risk of Cardiovascular Events
- FDA Approves Hetlioz: first treatment for non-24 hour sleep-wake disorder in blind individuals
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Approved Animal Drug Products Online (Green Book)
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Proposed Rule on Sanitary Transportation of Human and Animal Food
- From: U.S. Food & Drug Administration (FDA)
- Donar sangre es donar vida
- Parents can keep kids safe by talking about misusing prescription medications
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FSMA and Animal Feed - Comment Period Extensions
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Seeking Public Input on Animal Drug User Fee Act Information Collection
- From: U.S. Food & Drug Administration (FDA)
- YoungYou International Issues Voluntary Recall of Mega Slim Herbal Appetite Management Pills Due to Presence of DMAA
- From: U.S. Food & Drug Administration (FDA)
- Medical Device Safety and Recalls: Codman Neuro, TRUFILL n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System - Incorrect Instructions for Use
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for January 29, 2014
- From: U.S. Food & Drug Administration (FDA)
- Gano Excel USA Inc. Announces Recall of C’Real Spirulina
- From: U.S. Food & Drug Administration (FDA)
- ¿Tiene dudas sobre sus beneficios del Seguro Social?
- Pringles Issues Allergy Alert and Voluntary Recall of One Hour’s Worth of Production of Original Crisps Due to Undeclared Milk
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Annual Report to Congress on the Use of Mandatory Recall Authority Available
- From: U.S. Food & Drug Administration (FDA)
- ¿Ya recibió los papeles para preparar sus impuestos?
- Expertos de la Administración del Seguro Social responden preguntas del público
- Update of CVM's What's New - PMI Nutrition, LLC Recalls Red Flannel Cat Food Due to Possible Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- Winn-Dixie Recalls Instant Chocolate Drink Mix Sold in Florida
- From: U.S. Food & Drug Administration (FDA)
- PMI Nutrition, LLC Recalls Red Flannel® Cat Food Due to Possible Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- Araya Inc. Issues Allergy Alert on Undeclared Tree Nuts, Wheat, Milk and Soy in Their Chocolate Bars, Marshmallows, Dry Fruits and Chocolate Gift Boxes
- From: U.S. Food & Drug Administration (FDA)
- UPDATED: Allergy Allert - Undeclared Milk in Five Kinnikinnick Foods Products
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for January 22, 2014
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Cómo evitar a los estafadores y las llamadas de telemercadeo
- Lochiel Enterprises Limited Recalls St Mary’s River Smokehouses Oven Smoked Salmon Stix, Chili Mango Flavor Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Flat Creek Farm & Dairy Recalls Cheese Because of Possible Health Risk Update to Correcy Lot Number Information
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Trufill n-BCA Liquid Embolic System by Codman Neuro: Recall - Incorrect Instructions For Use
- FDA Hepatitis Update - Victrelis (boceprevir) label changes update contraindications and drug interactions
- From: U.S. Food & Drug Administration (FDA)
- FDA Classifies Worldwide Voluntary Correction Notice on TRUFILL® n-BCA Liquid Embolic System as Class I Recall
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Guidances Under Development for 2014
- From: U.S. Food & Drug Administration (FDA)
- FDA launches advisory committee membership nomination portal
- From: U.S. Food & Drug Administration (FDA)
- Rise’N Roll Bakery Issues Allergy Alert on Undeclared Egg in All Their Donut Varieties and Undeclared Peanuts in Nutty Crunch
- From: U.S. Food & Drug Administration (FDA)
- Merrell Food Group Issues Allergy Alert on Undeclared Peanut in “Crunch’N Nutter - Mixed Nut”
- From: U.S. Food & Drug Administration (FDA)
- Stemvida International Corporation Recalls StemAlive 90 Capsules Containing Undeclared Milk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - StemAlive 90 Capsules: Recall - Contains Undeclared Milk
- Día de Martin Luther King Jr.
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Cosmetics News Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Rohto Eye Drops - Mentholatum: Recall - Sterility Control Review
- Evite las estafas que parecen ser del Gobierno
- Cómo puede solicitar fondos del Gobierno para estudiar
- FDA Commissioner Margaret A. Hamburg's Statement on the 50th Anniversary Surgeon General's Report on Smoking and Health
- From: U.S. Food & Drug Administration (FDA)
- The Mentholatum Company Issues Voluntary Nationwide Recall of Rohto® Eye Drops Made in Vietnam
- From: U.S. Food & Drug Administration (FDA)
- Lo que necesita para declarar sus impuestos
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for January 15, 2014
- From: U.S. Food & Drug Administration (FDA)
- Mercado de Seguros Médicos y servicios preventivos
- Update of CVM's What's New - Current Animal Food GRAS Notices Inventory
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Veterinary Medication Errors
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Paskesz Candy Company Issues Allergy Alert on Undeclared Milk in Premium Belgian Chocolate Coins
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Acetaminophen Prescription Combination Drug Products with more than 325 mg: FDA Statement - Recommendation to Discontinue Prescribing and Dispensing
- FDA MedWatch - t:slim Insulin Cartridges by Tandem Diabetes Care: Recall - Potential for Cartridge Leak
- El robo de identidad y sus impuestos
- Midwest Wholesale Issues Voluntary Recall of Boost Ultra, XZone Gold, Sexy Monkey, Triple MiracleZen Platinum, Magic for Men, "New" Extenze, and New XZen Platinum Marketed as a Dietary Supplements Due to the Presence of Undeclared Drug Ingredients
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Puritan Bennett 840 Series Ventilator by Covidien - Class I Recall - Software Problem
[Index of Archives]
[CDC News]
[NIH News]
[Epson Inkjet]
[Yosemite]
