FDA News
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- FDA Permits Wright County Egg to begin shipping shell eggs to consumers
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Tentative approval of abacavir sulfate tablets, 60 mg
- From: U.S. Food & Drug Administration (FDA)
- FDA Office of Minority Health Website is live
- From: U.S. Food & Drug Administration (FDA)
- Recall of ROLAIDS® Extra Strength Softchews
- From: U.S. Food & Drug Administration (FDA)
- Recall of Tylenol Cold Liquid Products
- From: U.S. Food & Drug Administration (FDA)
- Recall of Children's BENADRYL® Allergy FASTMELT® Tablets and Junior Strength MOTRIN® Caplets
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - HiRes 90K Cochlear Implant Device: Recall - Malfunction
- Advanced Bionics Announces Voluntary Recall Of The Hires 90k Cochlear Implant
- From: U.S. Food & Drug Administration (FDA)
- Bravo Farms announces cheese recall, some products sold under Whole Foods Market label in 5 Western states
- From: U.S. Food & Drug Administration (FDA)
- WalkMed Infusion Issues Nationwide Recall of Triton Pole Mount Infusion Pumps
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 24, 2010
- From: U.S. Food & Drug Administration (FDA)
- RECALL: Organic Dark Chocolate Squares
- RECALL: Bravo Farms Recalls All Cheese
- Bravo Farms Cheese Recall
- From: U.S. Food & Drug Administration (FDA)
- Artisan Confections Recalls Dagoba new moon™ Rich Dark Chocolate 74% Cacao 0.32-Ounce Squares Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use Minor Species Designations List
- From: U.S. Food & Drug Administration (FDA)
- Krunchers! Inc. Recalls 18 Cases Of Jays Original Potato Chips Because Of Undeclared Milk Allergen
- From: U.S. Food & Drug Administration (FDA)
- FDA Basics Webinar: Melamine: The Cause of the Pet Food and Infant Formula Recalls
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA Basics Webinar: Melamine: The Cause of the Pet Food and Infant Formula Recalls
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Micromedics, Inc. Surgical Sealant Dispensers, Nasal Septal Buttons, and Otological Ventilation Tubes: Class 1 Recall-Weak or Open Seals
- KRUNCHERS! INC. RECALLS 18 CASES OF JAYS ORIGINAL POTATO CHIPS BECAUSE OF UNDECLARED MILK ALLERGEN
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Vigor-25: Undeclared Drug Ingredient - Sold as Natural Dietary Supplement
- FDA warns consumers not to use Vigor-25
- From: U.S. Food & Drug Administration (FDA)
- Interim Guidance on the Use of Influenza Antiviral Agents During the 2010-2011 Influenza Season
- From: U.S. Dept. of Health & Human Services
- FDA MedWatch - Propoxyphene: Withdrawal - Risk of Cardiac Toxicity
- Xanodyne agrees to withdraw propoxyphene from the U.S. market
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Xgeva to help prevent cancer-related bone injury
- From: U.S. Food & Drug Administration (FDA)
- NIH Experts Describe Influenza Vaccines of the Future
- From: U.S. Dept. of Health & Human Services
- Enforcement Report for November 17, 2010
- From: U.S. Food & Drug Administration (FDA)
- The Great American Smokeout
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Needleless Pre-filled Glass Syringes: Stakeholder Advisory - Compatibility Problems with Needleless Intravenous Access Systems
- Del Bueno Recalls Cheese Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA Warning Letters issued to four makers of caffeinated alcoholic beverages
- From: U.S. Food & Drug Administration (FDA)
- Liz Lovely Issues Voluntary Recall on Products Containing Chocolate Due to Undeclared Dairy from Chocolate Supplier
- From: U.S. Food & Drug Administration (FDA)
- Allergy Alert: Dried Taro with Sulfites
- NIH Scientists Explore 1510 Influenza Pandemic and Lessons Learned
- From: U.S. Dept. of Health & Human Services
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- S&M (U.S.A) Enterprise Corp Issues Alert on Undeclared Sulfites in Grow Grove Notes Brand Dried Taro
- From: U.S. Food & Drug Administration (FDA)
- FDA launches initiative to develop innovative external defibrillators
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new treatment option for late-stage breast cancer
- From: U.S. Food & Drug Administration (FDA)
- FDA Urges Consumers to be 'Smart' about Antibiotic Use
- From: U.S. Food & Drug Administration (FDA)
- RECALL: Costco Cheese Recalls
- RECALL: Smoked Turkey Breast Products
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Voluntary Recall of Bravo Farms Dutch Style Gouda Cheese Due to Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Gorgonzola Cheese Sold at Costco Recalled Due to Contamination With E.coli O157:H7
- From: U.S. Food & Drug Administration (FDA)
- DPI Specialty Foods Recalls Mauri Brand Gorgonzola Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA: Lot of Mauri Gorgonzola cheese positive for E. coli 0157:H7
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Sigma Spectrum Infusion Pump Model 35700: Class 1 Recall: Risk of Over-Infusion
- October 2010 Safety Labeling Changes: 34 Medical Product Labels with changes to Boxed Warnings, Contraindications, Precautions, Adverse Reactions
- RECALL: Mauri Gorgonzola cheese sold at Costco in Colorado
- Enforcement Report for November 10, 2010
- From: U.S. Food & Drug Administration (FDA)
- FDA: Lot of Mauri Gorgonzola cheese positive for E. coli 0157:H7
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Egrifta to Treat Lipodystrophy in HIV Patients
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Approval of Egrifta to treat lipodystrophy
- From: U.S. Food & Drug Administration (FDA)
- Pharmaceutical Company Lawyer Charged with Obstruction and Making False Statements
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - VITEK 2 Gram Negative Susceptibility Cards Containing Piperacillin/Tazobactam (TZP): Recall - Incorrect Test Results Observed
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA: Majority of drug and biological product makers meeting postmarketing requirements and commitments
- From: U.S. Food & Drug Administration (FDA)
- Cal-Maine Foods. Inc. Updates Voluntary Egg Recalls Information
- From: U.S. Food & Drug Administration (FDA)
- FDA working to prevent radiation overdoses during CT scans
- From: U.S. Food & Drug Administration (FDA)
- Allergy Alert: Fresh & Easy Ginger Spice Cookie Dough
- RECALL: Eggs
- RECALL: Products Containing Cilantro
- RECALL: Trader Joe's Chicken Pasta Salad
- RECALL: Apple Cider
- Update of CVM's What's New - Registration delayed until November 10: AAVPT Veterinary Drug Regulatory Life Cycle Course
- From: U.S. Food & Drug Administration (FDA)
- HRSA and FDA Present Health Education Awards
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Triton Pole Mount Infusion Pump by WalkMed: Recall - Potential Door Open Alarm Problem
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Cal-Maine Foods, Inc. Conducts Voluntary Egg Recall
- From: U.S. Food & Drug Administration (FDA)
- Orval Kent Food Company, Inc Voluntarily Recalls Products Containing Cilantro Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- WalkMed Infusion Issues Nationwide Recall of Triton Infusion Pump
- From: U.S. Food & Drug Administration (FDA)
- Baugher Enterprise, Inc. Recalls Baugher's Apple Cider Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Carefusion Recall of Alaris PC Units Model 8015 Classified as Class I Recall
- From: U.S. Food & Drug Administration (FDA)
- FDA, State of Maryland, and Baugher Enterprise warn consumers to avoid Baugher's Apple Cider
- From: U.S. Food & Drug Administration (FDA)
- RECALLS: Meat and Poultry Products in Illinois and New York
- RECALL: Unpasteurized Apple Cider
- The November 2010 FDA Patient Safety News is now available...
- From: U.S. Food & Drug Administration (FDA)
- DHMH Issues Consumer Alert Regarding Recall of Baugher's Apple Cider
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Registration Opens November 8: AAVPT Veterinary Drug Regulatory Life Cycle Course
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA, CDC, and Costco warn consumers to avoid Bravo Farms Dutch Style Gouda cheese
- From: U.S. Food & Drug Administration (FDA)
- FDA clears Cymbalta to treat chronic musculoskeletal pain
- From: U.S. Food & Drug Administration (FDA)
- ALERT: FDA, CDC, and Costco warn consumers to avoid Bravo Farms Dutch Style Gouda cheese
- FDA MedWatch - Hospira Symbiq One-Channel and Two-Channel Infusers: Class I Recall - Motor Encoder Failures
- Beaver Street Fisheries, Inc Voluntarily Recalls Tuna due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Actavis Encourages Consumers to Return Fentanyl Transdermal System 25 mcg/h
- From: U.S. Food & Drug Administration (FDA)
- Intelli Health Products, Issues a Voluntary Nationwide Recall of Duro Extend Capsules for Men Marketed as Dietary Supplements
- From: U.S. Food & Drug Administration (FDA)
- FDA, USDA, Cornell University announce alliance for produce safety
- From: U.S. Food & Drug Administration (FDA)
- FDA reclassifies certain digital mammography devices today
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for November 3, 2010
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- New Study Re-examines Bacterial Vaccine Studies Conducted During 1918 Influenza Pandemic
- From: U.S. Dept. of Health & Human Services
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- MedSun Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - October 2010 Green Book Monthly Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Octopus Nuvo Tissue Stabilizer: Recall - Potential for Device Fracture
- FDA Classifies Previous Field Action of Medtronic Surgical Device as Class I Recall
- From: U.S. Food & Drug Administration (FDA)
- FDA, University of Rochester announce partnership for new drug products
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new indication for Afinitor
- From: U.S. Food & Drug Administration (FDA)
- New Video for Women with Diabetes
- From: U.S. Food & Drug Administration (FDA)
- Kosher First LLC. Issues Alert on Listeria in Tuv Taam Salads Nova Lox Salad
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Teflaro for Bacterial Infections
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Heparin Sodium (B. Braun): Recall - Trace Contaminant
- B. Braun Voluntarily Recalls Seven Lots of Heparin Manufactured in 2008 Due to Supplier-Initiated Recall of Heparin Active Pharmaceutical Ingredient (API)
- From: U.S. Food & Drug Administration (FDA)
- NOAA and FDA Announce Chemical Test for Dispersant in Gulf Seafood;
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Methotrexate Injection, 50mg/2mL and 250mg/10mL Vials: Recall - Presence of Glass Particulates
- FDA approves Latuda to treat schizophrenia in adults
- From: U.S. Food & Drug Administration (FDA)
- Vaccines and Related Biological Products Advisory Committee Update
- From: U.S. Food & Drug Administration (FDA)
- Sandoz initiates voluntary recall in the US of all 50mg/2mL and 250mg/10mL vials of Methotrexate Injection, USP due to the presence of glass particulates
- From: U.S. Food & Drug Administration (FDA)
- FDA approves additional medical indication for Sprycel
- From: U.S. Food & Drug Administration (FDA)
- RECALL: Autentico Pork Skins & Pork Products in CA
- Enforcement Report for October 27, 2010
- From: U.S. Food & Drug Administration (FDA)
- bioMérieux, Inc. Issues Urgent Product Correction for VITEK® 2 Gram Negative Susceptibility Cards Containing Piperacillin/Tazobactam
- From: U.S. Food & Drug Administration (FDA)
- U.S. Marshals seize FDA-regulated food stored at rodent-infested warehouse in Georgia
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Announces Addition of Boxed Warning to METACAM® (meloxicam) Labels
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Safe Animal Feed Video Available
- From: U.S. Food & Drug Administration (FDA)
- FDA awards $18.5 million in grants for food and feed safety
- From: U.S. Food & Drug Administration (FDA)
- Federal government takes action against Tennessee food distributor
- From: U.S. Food & Drug Administration (FDA)
- Federal Government has seized Tri-Med Labs drug products
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FY 2011 Nationwide Assignment to Collect and Analyze Samples of Direct-Human-Contact Feed for Salmonella
- From: U.S. Food & Drug Administration (FDA)
- FDA laboratory receives accreditation
- From: U.S. Food & Drug Administration (FDA)
- RECALL: Tomi Dried Seafood Products, Botulism Risk
- ALLERGY ALERT: Nestle Raisinets
- RECALL: Market Pantry Beef Sticks
- Mega Pops Manufacturer Leads Effort with Retailers to Recall Product Voluntarily During Review of Customer Concerns
- Mega Pops Manufacturer Leads Effort with Retailers to Recall Product Voluntarily During Review of Customer Concerns
- From: U.S. Food & Drug Administration (FDA)
- Working with FDA, Standard Homeopathic Company Voluntarily Recalls Hyland's Teething Tablets to Address Manufacturing Process
- From: U.S. Food & Drug Administration (FDA)
- Nestle® USA Issues Allergen Alert on Single Production Code of Nestle® Raisinets® Fun Size Bags
- From: U.S. Food & Drug Administration (FDA)
- DSHS Orders Sangar Produce to Close, Recall Products
- From: U.S. Food & Drug Administration (FDA)
- FDA heightens focus on retail food safety
- From: U.S. Food & Drug Administration (FDA)
- Hyland's Teething Tablets may pose a risk to children
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Western Milling LLC Voluntarily Recalls Universal Turkey and Kruse G.B. Turkey Grower Feeds Because of Possible Health Risk to Animals
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Hyland's Teething Tablets: Recall - Risk of Harm to Children
- HIV/AIDS Update - Invirase (saquinavir) labels updated with important risk information about abnormal heart rhythms
- From: U.S. Food & Drug Administration (FDA)
- 2010-2011 Seasonal Influenza (Flu) Vaccine Safety
- From: U.S. Dept. of Health & Human Services
- Western Milling LLC Voluntarily Recalls Universal Turkey and Kruse G.B. Turkey Grower Feeds Because of Possible Health Risk to Animals
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Fentanyl Transdermal System: Recall - Potential for Active Ingredient to Release Faster Than Specified
- FDA Heightens Focus on Retail Food Safety
- From: U.S. Food & Drug Administration (FDA)
- Foremost Foods International, Inc. Issues Recall on Certain Tomi Dried Seafood Products
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Del Monte Fresh Produce N.A., Inc. Announces Limited Voluntary Cantaloupe Recall In And Around Detroit, Michigan
- Actavis Inc. Issues a Voluntary Recall of 18 Lots of Fentanyl Transdermal System 25 mcg/h
- From: U.S. Food & Drug Administration (FDA)
- Del Monte Fresh Produce N.A., Inc. Announces Limited Voluntary Cantaloupe Recall In And Around Detroit, Michigan
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Invirase (saquinavir): Label Change - Risk of Abnormal Heart Rhythm
- New Label Changes for Commonly Prescribed HIV Drug Invirase
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - additional Veterinary Medicine Advisory Committee materials posted
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 20, 2010
- From: U.S. Food & Drug Administration (FDA)
- September 2010 Safety Labeling Changes: 37 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions
- Medicines in My Home Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - GnRH Agonists: Label Change - Increased Risk of Diabetes and Cardiovascular Disease (Update)
- FDA: Include warnings on risk for class of prostate cancer drugs
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Pradaxa to prevent stroke in people with atrial fibrillation
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update -Tentative approval of lamivudine and stavudine Fixed Dose Combination tablets, 150/300 mg
- From: U.S. Food & Drug Administration (FDA)
- FDA Basics Webinar: Food Emergency Response Network (FERN)
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Tylenol 8 Hour Caplets 50 Count: Recall - Uncharacteristic musty or moldy odor
- McNeil Consumer Healthcare Announces Voluntary Recall of One Product Lot of TYLENOL® 8 Hour Caplets 50 Count Sold in The United States and Puerto Rico
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Botox to treat chronic migraine
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Presentations from the September 20, 2010 Veterinary Medicine Advisory Committee Meeting
- From: U.S. Food & Drug Administration (FDA)
- FDA Provides Update on LASIK Quality of Life Collaboration Project Status
- From: U.S. Food & Drug Administration (FDA)
- FDA Authorizes Hillandale Farms to Begin Shipping Fresh Shell Eggs
- From: U.S. Food & Drug Administration (FDA)
- FDA Issues Warning Letter to Wright County Egg
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - New Baraclude (entecavir) Tablets and Oral Solution dosing regimen for chronic hepatitis B (HBV) and decompensated liver disease
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Pre-Registration Notice: AAVPT Veterinary Drug Regulatory Life Cycle Course
- From: U.S. Food & Drug Administration (FDA)
- **CONSUMER ALERT** Pats Exotic Beverage Recalls "Carrot Juice" Beverage, "Carrot Beet" Beverage, "Carrot Lime" Beverage and "Cucumber" Beverage Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- RECALL: Frozen Green Pea Products Sold at Kroger & Walmart
- The Pictsweet Company Announces a Voluntary Recall of Frozen Green Peas Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves Botox to treat chronic migraine
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Excelsior Medical 5 ml Fill in 6 cc Prefilled Saline Flush Syringes: Recall - Potential Loss of Sterility
- FDA MedWatch - CareFusion Corporation Alaris PC Units (Model 8015): Recall - Potential for Delay or Interruption of Therapy
- ALLERGY ALERT: Breaded Okra
- CVM Updates - FDA Announces Letter to Industry on Marketing of Animal Food Substances as Generally Recognized As Safe (GRAS)
- From: U.S. Food & Drug Administration (FDA)
- The Pictsweet Company Issues Allergy Alert On Undeclared Milk In 32 Ounce Clear Bag Breaded Okra
- From: U.S. Food & Drug Administration (FDA)
- Excelsior Medical Recall of 5 ml Fill in 6 cc Prefilled Saline Flush Syringes Classified as a Class I Recall
- From: U.S. Food & Drug Administration (FDA)
- FDA participates in 'International Internet Week of Action'
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Chelation Products: Unapproved Over-the-Counter Drugs - Consumer Warning
- FDA Determines Knee Device Should Not Have Been Cleared for Marketing
- From: U.S. Food & Drug Administration (FDA)
- FDA issues warnings to marketers of unapproved 'chelation' products
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Government takes action against Montana drug manufacturer
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Cumulative Veterinary Adverse Drug Experience (ADE) Reports - Updated September 30, 2010
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 13, 2010
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Bisphosphonates (Osteoporosis Drugs): Label Change - Atypical Fractures Update
- FDA: Possible increased risk of thigh bone fracture with bisphosphonates
- From: U.S. Food & Drug Administration (FDA)
- FDA schedules third orphan drug workshop for Nov. 4-5, 2010
- From: U.S. Food & Drug Administration (FDA)
- FDA approves injectable drug to treat opioid-dependent patients
- From: U.S. Food & Drug Administration (FDA)
- RECALL: BLUE brand dog food
- RECALL: "La Nuestra" Mamey Ice Cream
- Update of CVM's What's New - Blue Buffalo Company, Ltd. Recalls Limited Production Code Dates of Dry Dog Food Because of Possible Excess Vitamin D
- From: U.S. Food & Drug Administration (FDA)
- LIPITOR Recall Information
- From: U.S. Food & Drug Administration (FDA)
- Blue Buffalo Company, Ltd. Recalls Limited Production Code Dates of Dry Dog Food Because of Possible Excess Vitamin D
- From: U.S. Food & Drug Administration (FDA)
- Influenza Activity - United States and Worldwide, June 13--September 25, 2010
- From: U.S. Dept. of Health & Human Services
- Influenza Vaccination Coverage among Children Aged 6-23 Months - U.S., 2008-09 Influenza Season
- From: U.S. Dept. of Health & Human Services
- Seasonal Flu Information for Businesses and Employees
- From: U.S. Dept. of Health & Human Services
- Final Estimates for 2009-10 Seasonal Influenza and Influenza A (H1N1) 2009 Monovalent Vaccination Coverage - U.S., August, 2009 through May, 2010
- From: U.S. Dept. of Health & Human Services
- RECALL: Smoked Fish
- Montalvan's Sales, Inc. Recalls "La Nuestra" Brand Mamey Ice Cream Because of Potential Health Risk
- 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)
- D & M Smoked Fish, Inc. is Recalling Specific Lots of Haifa Smoked Fish Brand Products Sold Between August 10, 2010 and September 3, 2010 Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Slimming Beauty Bitter Orange Slimming Capsules: Undeclared Drug Ingredient
- FDA MedWatch - Meridia (sibutramine): Market Withdrawal Due to Risk of Serious Cardiovascular Events
- Abbott Laboratories agrees to withdraw its obesity drug Meridia
- From: U.S. Food & Drug Administration (FDA)
- FDA: Potentially harmful stimulant found in Slimming Beauty capsules
- From: U.S. Food & Drug Administration (FDA)
- Gaspari Nutrition Nutrition Issues a Voluntary Nationwide Recall of Novedex XT, a Product Marketed as a Dietary Supplement Containing ATD
- From: U.S. Food & Drug Administration (FDA)
- Living Foods Inc. Initiates a Voluntary Market Withdrawal of Alfalfa Sprouts Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- RECALL: Alfalfa Sprouts
- FDA seeks to stop juice company's processing, distribution
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for October 6, 2010
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA awards $904,000 to Pan American Health Organization for information 'hub'
- From: U.S. Food & Drug Administration (FDA)
- FDA Issues Regulatory Science Report
- From: U.S. Food & Drug Administration (FDA)
- FDA Basic Video: Margaret Oeller (Video)
- From: U.S. Food & Drug Administration (FDA)
- How does FDA plan to enforce the restrictions on promotion and advertising established by the Tobacco Control Act?
- From: U.S. Food & Drug Administration (FDA)
- FDA Basic Video: Diane Murphy Discusses Vaccines (Video)
- 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)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- ALLERGY ALERT: White bread with nuts not listed on the label
- Learn More about New Health Care Benefits - HealthCare.Gov
- From: U.S. Food & Drug Administration (FDA)
- Lucerne Foods Voluntarily Recalls Oregon Western Hazelnut Bread Sold at Safeway and WinCo stores in 12 States Due to Undeclared Nut Content
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Approval Pathway for Biosimilar and Interchangeable Biological Products Public Meeting Nov. 2-3
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Approval Pathway for Biosimilar and Interchangeable Biological Products, FDA Public Meeting
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA awards nearly $3 million for TB research
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - FDA's Animal Feed Safety System (AFSS) Project Plans Update #7
- From: U.S. Food & Drug Administration (FDA)
- The October 2010 FDA Patient Safety News is now available...
- From: U.S. Food & Drug Administration (FDA)
- Q and A: Vaccine Selection for the 2010-2011 Influenza Season
- From: U.S. Dept. of Health & Human Services
- FDA schedules public hearing on Biologics Price Competition and Innovation Act
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Rising Dough Bakery Issues Allergy Alert on Undeclared Walnuts in the Rising Dough Brand Individual Wrapped Cranberry Muffins
- From: U.S. Food & Drug Administration (FDA)
- Insurer Pricing and Denial Rates Now on HealthCare.gov
- HIV/AIDS Update - Tentative approval of abacavir sulfate tablets, 300 mg
- From: U.S. Food & Drug Administration (FDA)
- ALLERGY ALERT: Hostess® Mini Muffins (Chocolate Chip variety)
- CVM Updates - CVM Announces Availability of Online Pet Pharmacy Brochure through Pueblo, Colorado
- From: U.S. Food & Drug Administration (FDA)
- Hostess Brands, Inc. Issues Voluntary Recall of Hostess® Mini Muffins (Chocolate Chip variety) Due to Unlabeled Allergen
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Vaccines and Related Biological Products Advisory Committee Update
- From: U.S. Food & Drug Administration (FDA)
- Hostess Brands, Inc. Issues Voluntary Recall of Hostess® Mini Muffins (Chocolate Chip variety) Due to Unlabeled Allergen
- From: U.S. Food & Drug Administration (FDA)
- FDA Orders Halt to Marketing of Unapproved Single-Ingredient Oral Colchicine
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 29, 2010
- From: U.S. Food & Drug Administration (FDA)
- BARDA Funds Development of Next-Generation Portable Ventilators
- From: U.S. Dept. of Health & Human Services
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- The October 2010 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Health Requirements and Recommendations for Travel to Saudi Arabia During the 2010 Hajj: Information for U.S. Travelers
- From: U.S. Dept. of Health & Human Services
- FDA MedWatch - Infant sleep positioners: Consumer Warning - Risk of Suffocation
- Deaths prompt CPSC, FDA warning on infant sleep positioners
- From: U.S. Food & Drug Administration (FDA)
- Pfizer Consumer Healthcare Issues Voluntary Recall of One Lot of ThermaCare HeatWraps Menstrual Product
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns three companies to stop making unproven claims on mouth rinses
- From: U.S. Food & Drug Administration (FDA)
- NIH and FDA announce awards to advance regulatory science
- From: U.S. Food & Drug Administration (FDA)
- ALLERGY ALERTS: Granola Thins, Butter Cup Cakes, Pork Ginger Sausage
- FDA issues final rule on safety information during clinical trials
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- HealthCare.gov on Facebook
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Amgen Initiates Voluntary Nationwide Recall Of Certain Lots Of Epogen® And Procrit® (Epoetin Alfa)
- From: U.S. Food & Drug Administration (FDA)
- FDA approves combination contraceptive containing a folate
- From: U.S. Food & Drug Administration (FDA)
- Similac Powder Infant Formulas: Recall-UPDATE: new searchable database and consumer update added
- FDA MedWatch - Octagam (Immune Globulin Intravenous (human)) 5% Liquid Preparation: Market Withdrawal - Risk of Thromboembolic Events
- FDA MedWatch - Epogen and Procrit (epoetin alfa): Recall - Particulate Matter in Vials
- FDA MedWatch - Electric Dental Handpieces and Electric Oral Bone-cutting Handpieces: Safety Investigation of Patient Burns
- U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 22, 2010
- From: U.S. Food & Drug Administration (FDA)
- Similac Infant Formula: Get a Complete List of Products Recalled
- CVM Updates - FDA to hold Public Workshop for Animal Health Industry on Release of Beta-Version of eSubmitter, an Electronic Submission Tool
- From: U.S. Food & Drug Administration (FDA)
- Red Lotus Bakery Issues Allergy Alert On Undeclared Eggs In "Butter Cup Cakes"
- From: U.S. Food & Drug Administration (FDA)
- General Mills Issues Voluntary Class One Recall of One Day's Production of Nature Valley Dark Chocolate Flavor Granola Thins
- From: U.S. Food & Drug Administration (FDA)
- Six Months of the Affordable Care Act
- FoodSafety.gov News & Features Update
- FDA MedWatch - Avandia (rosiglitazone): REMS - Risk of Cardiovascular Events
- FDA significantly restricts access to the diabetes drug Avandia
- From: U.S. Food & Drug Administration (FDA)
- ALLERGY ALERT: Western Family Maple Nut Ice Cream
- FDA MedWatch - Similac Powder Infant Formulas: Recall
- RECALL: Similac Powder Infant Formula
- Deluxe Ice Cream Issues Allergy Alert on Undeclared Peanuts in Western Family Maple Nut Ice Cream
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Suzipoo Issues Allergy Alert on Undeclared Allergen in Lobster Poo
- From: U.S. Food & Drug Administration (FDA)
- Abbott Voluntarily Recalls Certain Similac® Brand Powder Infant Formulas That Did Not Meet Its Quality Standards
- From: U.S. Food & Drug Administration (FDA)
- ALLERGY ALERT: Garvi Gujarat brand Tam Tam (star noodle snack)
- House of Spices Issues Allergy Alert On Undeclared Peanuts in Garvi Gujarat Brand Tam Tam (Star Noodles) 10 oz.
- From: U.S. Food & Drug Administration (FDA)
- NIH study models H1N1 flu spread
- From: U.S. Dept. of Health & Human Services
- FDA approves first oral drug to reduce MS relapses
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - CVM Annual Report for Fiscal Year 2009
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Announces Minor Use/Minor Species Grant Program Awards
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Aromatase Inhibitors in Products Marketed as Dietary Supplements: Recall
- ALLERGY ALERT: Oatmeal Raisin Cookies & Chocolate Chunk Cookies Sold at 7-eleven
- Hallmark Fisheries Issues Recall of Crab Meat Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Dough Masters Inc. Issues Recall of Oatmeal Raisin Cookies and Chocolate Chunk Cookies Due to Undeclared Walnuts
- From: U.S. Food & Drug Administration (FDA)
- iForce Nutrition Issues a Voluntary Nationwide Recall of Reversitol a Product Marketed as a Dietary Supplement Containing ATD
- From: U.S. Food & Drug Administration (FDA)
- FDA Office of Women's Health Fall 2010 eUpdate
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Actos (pioglitazone): Ongoing Safety Review - Potential Increased Risk of Bladder Cancer
- FDA reviewing preliminary safety information on Actos (pioglitazone)
- From: U.S. Food & Drug Administration (FDA)
- Advanced Muscle Science Issues a Voluntary Nationwide Recall of AROM-X Capsules, AROM-X UTT Liquid, AROM-XL Liquid, 4-AD Capsules and Decavol Capsules Marketed as a Dietary Supplements Containing ATD
- From: U.S. Food & Drug Administration (FDA)
- Fizogen Precision Technologies, Inc. Issues a Voluntary Nationwide Recall of OFF CYCLE II HARDCORE, a Product Marketed as a Dietary Supplement
- From: U.S. Food & Drug Administration (FDA)
- FDA , U. of Md., train Bangladeshis on aquaculture safety
- From: U.S. Food & Drug Administration (FDA)
- FDA hosts Middle East and North Africa food safety experts
- From: U.S. Food & Drug Administration (FDA)
- FDA approves devices for heart failure patients
- From: U.S. Food & Drug Administration (FDA)
- Twitter Chat at 3:30 pm ET Today: Food Safety for At-Risk People
- G.E.T. Issues Vouluntary Recall of ArimaDex
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) FDA/CFSAN Color Additive News Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - September Green Book Update
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Kilosports Inc. Issues Voluntary Recall of Clomed
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 15, 2010
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - BagEasy Manual Resuscitation Devices by Westmed, Inc.: Class 1 Recall
- August 2010 Drug Safety Labeling Changes: 24 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions
- Westmed, Inc. Issues Nationwide Recall of BagEasy Manual Resuscitation Devices
- From: U.S. Food & Drug Administration (FDA)
- Forest Pharmaceuticals agrees to guilty plea for violating FDA laws
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Valcyte (valganciclovir hydrochloride) Label Change: Possible overdose in pediatric patients
- FDA issues new dosing guide for children using Valcyte
- From: U.S. Food & Drug Administration (FDA)
- The Affordable Care Act & Behavioral Health
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA approves new drug for gout
- From: U.S. Food & Drug Administration (FDA)
- Webinar on Generic Drugs
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Availability of draft guidance re: development of antivirals for Chronic Hepatitis C, including coinfection with HIV
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Availability of draft Guidance: Chronic Hepatitis C Virus Infection: Developing Direct-Acting Antiviral Agents for Treatment
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov News & Features Update
- FoodSafety.gov Recall: Libby & Kroger Corned Beef, Brushy Creek Beef Products
- HIV/AIDS Update - Tentiative approval of lamivudine, nevirapine, and stavudine fixed dose combination tablets, 150 mg/200 mg/30 mg
- From: U.S. Food & Drug Administration (FDA)
- Influenza Vaccination Information for Health Care Workers
- From: U.S. Dept. of Health & Human Services
- How to Clean and Disinfect Schools to Help Slow the Spread of Flu
- From: U.S. Dept. of Health & Human Services
- Get information about high-risk groups, flu symptoms and emergency warning signs, and get CDC recommendations.
- From: U.S. Dept. of Health & Human Services
- FDA MedWatch - Hospira Symbiq One-Channel and Two-Channel Infusers: Class I Recall - Potential for device to fail to detect air in line
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Gadolinium-based Contrast Agents: Class Labeling Change - Risk of Nephrogenic Systemic Fibrosis
- FDA approves pediatric use of chemical poisoning treatment
- From: U.S. Food & Drug Administration (FDA)
- The September 2010 FDA Patient Safety News is now available...
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
- From: U.S. Food & Drug Administration (FDA)
- FDA acts against 5 electronic cigarette distributors
- From: U.S. Food & Drug Administration (FDA)
- FDA: New warnings required on use of gadolinium-based contrast agents
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recall: Milk
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Recall of Fluid Milk Products out of Midland Farms, Inc.
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for September 8, 2010
- From: U.S. Food & Drug Administration (FDA)
- How the Affordable Care Act Will Help Businesses and Unions Keep Early Retirees Covered
- FDA MedWatch - AngioSculpt "EX" PTCA Scoring Balloon Catheter by AngioScore, Inc.: Recall - Risk of Catheter Separation
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Undeclared Sulfites in "Rehmat" Brand Apricots
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - The Hartz Mountain Corporation Recalls Hartz Naturals Real Beef Treats Because of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Warning: Discard cheeses from Estrella Family Creamery
- Cibo Vita issues Allergy Alert on Undeclared Sulfites in Mediterranean Mix of Woodpecker Brand
- FoodSafety.gov Recall: Hartz Naturals Real Beef Treats for Dogs
- FoodSafety.gov Recall: Egg Noodles & Wonton Skins, Possible Salmonella
- Sparboe Farms Provides Clarification on its Voluntary Recall of Fresh Shell Eggs
- From: U.S. Food & Drug Administration (FDA)
- The Hartz Mountain Corporation Recalls Hartz Naturals Real Beef Treats Because of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Real Taste Noodle Manufacture Recalls Egg Noodle Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA cautions consumers about Estrella Family Creamery cheeses
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Additional Materials for the AquAdvantage Salmon VMAC Meeting
- From: U.S. Food & Drug Administration (FDA)
- Good Taste Noodle MFG Recalls "Egg Noodles and Wonton Skins" Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls: Whole Foods Recalls Raw Goat Milk Cheese
- Whole Foods Market® Announces Recall of Morningland Dairy and Ozark Hills Farm Cheese
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Tentiative approval of lamivudine, nevirapine, and stavudine fixed dose combination tablets, 150 mg/200 mg/30 mg
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recall: Cooked Shredded Pork Skin Products
- FoodSafety.gov Recall Expanded: Queso Fresco and Requeson (Ricotta)
- Enforcement Report for September 1, 2010
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- What do consumers need to know about the recall of shell eggs?
- From: U.S. Food & Drug Administration (FDA)
- Azteca Linda Corp. Expands Recall of Queso Fresco Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - P&G Voluntarily Recalls a Small Amount of Dry Cat Food
- From: U.S. Food & Drug Administration (FDA)
- P&G Voluntarily Recalls a Small Amount of Dry Cat Food
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov News Update
- FoodSafety.gov Recall: Iams Cat Food Recalled from Stores in Loveland, Colorado
- QUESERIA CHIPILO INC. Recalls Cheese Products because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Tygacil (tigecycline): Label Change - Increased Mortality Risk
- FoodSafety.gov Allergy Alert: Peanuts in "Mixed Nuts Fancy, No Peanuts"
- FoodSafety.gov Recall: Morningland Dairy & Ozark Hills Farm cheeses
- The September 2010 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - new guidances available
- From: U.S. Food & Drug Administration (FDA)
- Torn & Glasser Issues Allergy Alert on Undeclared Peanuts Fancy, No Peanuts
- From: U.S. Food & Drug Administration (FDA)
- FDA seeks court order against Michigan dairy
- From: U.S. Food & Drug Administration (FDA)
- Vaccines and Related Biological Products Advisory Committee Update
- From: U.S. Food & Drug Administration (FDA)
- Paleta California Co. Announces Voluntary Recall of Frozen Mamey Paletas Because of Potential Contamination with Salmonella Typhi
- From: U.S. Food & Drug Administration (FDA)
- Morningland Dairy Conducting Nationwide Voluntary Recall of All Cheese Labeled as Morningland Dairy & Ozark Hills Farm Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA launches new organizational performance management system
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Green Book August 2010 Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - P&G Recalls Small Number of Bags of Cat Food From Stores in Loveland, Colorado
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls: "Fruiti Pops" Mamey Frozen Fruit Bars and Queseria Chipilo Cheese Products
- P&G Recalls Small Number of Bags of Cat Food From Stores in Loveland, Colorado
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recall: Ground Beef Distributed to BJ's Wholesale Club
- Sparboe Farms Initiated Voluntary Recall Fresh Shell Eggs
- From: U.S. Food & Drug Administration (FDA)
- Fruiti Pops, Inc. Recalls "Fruiti Pops" Brand Mamey Frozen Fruit Bars Because of Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Queseria Chipilo Recalls Cheese Products Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Cal-Maine Foods, Inc. Clarifies Previous Statement on Nationwide Shell Egg Recall
- From: U.S. Food & Drug Administration (FDA)
- Estimating Seasonal Influenza-Associated Deaths in the U.S: CDC Study Confirms Variability of Flu
- From: U.S. Dept. of Health & Human Services
- FDA MedWatch - Huber Needles: Recall - Risk of Coring
- FDA MedWatch - Fingerstick Devices to Obtain Blood Specimens: Initial Communication - Risk of Transmitting Bloodborne Pathogens
- Enforcement Report for August 25, 2010
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Trafficanda Egg Ranch Initiates Voluntary Recall of Medium, Large, X Large, & Jumbo AA Cartons; 5 Dozen Medium Over Wrap & 20 Count Over Wrap, Fresh Shell Eggs Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Cardenas Market Brand Label Included in Wright County Egg Recall
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns Consumers to Avoid TimeOut Capsules
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls: Queso Fresco and Queso Hebra
- Azteca Linda Corp. Recalls Queso Fresco and Queso Hebra because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Veterinary Medicine Advisory Committee Meeting Announcement
- From: U.S. Food & Drug Administration (FDA)
- Natural Wellness, Inc. Issues a Nationwide Voluntary Recall of Masxtreme Capsules, Marketed as a Dietary Supplement - 08/24/10
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Alert: Updated List of Recalled Egg Brands
- The Power of Information at Your Fingertips
- 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) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Mr. Magic Male Enhancer: Undeclared Drug Ingredient
- FDA releases guidance on federal menu labeling requirements
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns of Possible Dangers from Portable Foot-Tanning Device
- From: U.S. Food & Drug Administration (FDA)
- Integra Issues URGENT Worldwide Recall of NeuroBalloonTM Catheter
- From: U.S. Food & Drug Administration (FDA)
- Moark, LLC, of Fontana, California, Recalls Shell Eggs Supplied From Hillandale Farms of Iowa Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Update: NuCal Foods Conducts Recall of Shell Eggs Supplied from Hillandale Farms of Iowa Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls: 380,000 lbs of Deli Meat Products, Possible Listeria
- FDA MedWatch - INOMAX DS Drug-Delivery System: Class I Recall - Risk of Interruption of Drug Flow
- NY Fish Inc Issues an alert on uneviscerated fish
- From: U.S. Food & Drug Administration (FDA)
- Study: Presence of murine leukemia virus found in CFS Patients, others
- From: U.S. Food & Drug Administration (FDA)
- NIH Office of Research on Women's Health - 20th Anniversary Celebration
- From: U.S. Food & Drug Administration (FDA)
- Luberski Inc. Initiates Voluntary Recall of Large Fresh Shell Eggs Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update - Tentative approval of generic atazanavir sulfate capsules, 300 mg
- From: U.S. Food & Drug Administration (FDA)
- Milton's Baking Voluntarily Recalls 24 oz. Multi-Grain Bread in Three States For Undeclared Milk in Some Loaves
- From: U.S. Food & Drug Administration (FDA)
- GloryBee Foods Recalls Whole Raw Pistachio and Whole Raw Pistachio Kernels Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Austinuts Wholesale, Inc. Announces Voluntary Recall of Pistachio Kernel Products
- From: U.S. Food & Drug Administration (FDA)
- Review Calls for New Federal Approach to Medical Countermeasures
- From: U.S. Dept. of Health & Human Services
- Salmonella in Alfalfa Sprouts
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Alert: URGENT Nationwide Frozen Mamey Fruit Pulp Recall
- Hillandale Farms of Iowa Conducts Nationwide Voluntary Recall of Shell Eggs Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Urgent Nationwide Frozen Mamey Fruit Products Recall
- From: U.S. Food & Drug Administration (FDA)
- Stalevo(carbidopa/levodopa and entacapone): Ongoing Safety Review: Possible increased cardiovascular risk
- FoodSafety.gov Alert: URGENT Nationwide Egg Recall
- FoodSafety.gov Recalls: "La Nuestra" Frozen Mamey Pulp
- Montalvan's Sales, Inc. Recalls "La Nuestra" Brand Frozen Mamey Because of Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Urgent Nationwide Egg Recall
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Updated Minor Use/Minor Species Designations List
- From: U.S. Food & Drug Administration (FDA)
- COUNTRY Eggs, Inc. Initiates Voluntary Recall of Large AA Loose 15 dozen Fresh Shell Eggs Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- U.S. Marshals seize food from rodent-infested Ga. warehouse
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 18, 2010
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recall: Nationwide Egg Recall Expanded
- Wright County Egg Expands Nationwide Voluntary Recall of Shell Eggs Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- NuCal Foods Conducts Recall of Shell Eggs Supplied from Wright County Egg Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- J & H Besta Expands Nationwide Recall of Slim- 30 Herb Supplement to Include Lot 6032101 Found to Contain an Undeclared Drug Ingredient
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Moonstruck Chocolate Co. Issues Nationwide Allergy Alert on Undeclared Peanut-Butter Filling in Their 4 Piece Cream Cone Chocolate Truffle Collection and 12 Piece Chocolate Malted (or Malt) Cream Cone Chocolate Truffles
- From: U.S. Food & Drug Administration (FDA)
- Glow Industries, Inc. Issues Nationwide Recall of Mr. Magic Male Enhancer from Don Wands Amended
- From: U.S. Food & Drug Administration (FDA)
- Undeclared Sulfites in "Golden Bridge" Dried Dates
- From: U.S. Food & Drug Administration (FDA)
- Elie Baking Corp issues Allergy Alert on Undeclared Soy in Food City brand Low-Carb Tortilla White and Whole Wheat 10 count
- From: U.S. Food & Drug Administration (FDA)
- NBTY Acquisition LLC Dba Leiner Health Products Issues Allergy Alert on Undeclared Soy in Air Shield Effervescent Tablets, Air Protector Effervescent Tablets, Immune System Support Effervescent, and Airhealth Effervescent Tablets And Stick Packs
- From: U.S. Food & Drug Administration (FDA)
- How the Affordable Care Act Will Hold Insurers Accountable
- Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports
- From: U.S. Food & Drug Administration (FDA)
- CDRH/FDA Public Webinar: FDA Discussion on the Draft 510(k) and Use of Science in Regulatory Decision Making Reports
- From: U.S. Food & Drug Administration (FDA)
- How is a potential advisory committee member screened for conflicts of interests?
- From: U.S. Food & Drug Administration (FDA)
- What are the qualifications of a scientific member of an advisory committee?
- From: U.S. Food & Drug Administration (FDA)
- What is a financial conflict of interest waiver?
- From: U.S. Food & Drug Administration (FDA)
- What is a conflict of interest?
- From: U.S. Food & Drug Administration (FDA)
- What is an FDA Advisory Committee?
- From: U.S. Food & Drug Administration (FDA)
- How does an individual become a member of an FDA advisory committee?
- From: U.S. Food & Drug Administration (FDA)
- Nationwide Milk Allergen Recall of Kroger "Meals Made Simple Shrimp Linguini"
- From: U.S. Food & Drug Administration (FDA)
- Merrick Pet Care Recalls Filet Squares & Texas Hold'ems 10oz Bag (Item # 60016 All Lots) Because of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Staphylococcus Aureus in Queso Cotija Cheese
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recalls: Frozen Mamey Fruit Pulp and Queso Cotija Cheese
- FDA MedWatch - Midodrine hydrochloride: FDA Proposes Withdrawal of Low Blood Pressure Drug
- Update of CVM's What's New - New Issue of FDA Veterinarian Newsletter
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Merrick Pet Care Recalls Filet Squares & Texas Hold'ems 10oz Bag (Item # 60016 All Lots) Because of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA Proposes Withdrawal of Low Blood Pressure Drug
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Guidance - Residual Solvents in New Veterinary Medicinal Products
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov: Nationwide Egg Recall, Illnesses Reported
- Wright County Egg Conducts Nationwide Voluntary Recalls of Shell Eggs Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Goya Foods, Inc. Announces Voluntary Recall of Frozen Mamey Pulp, Produced By Coco, S.A. of Guatemala Because of Potential Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA approves ella[TM] tablets for prescription emergency contraception
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - 6 French Engage Introducer Devices by St. Jude Medical: Recall - Potential for Separation of Shaft From Hub
- What is an FDA Drug Safety Communication?
- From: U.S. Food & Drug Administration (FDA)
- How does the FDA use Advisory Committees to make decisions about drugs?
- From: U.S. Food & Drug Administration (FDA)
- Strong America Ltd. Issues an Alert on Undeclared Sulfites in Golden Smell Brand "Dried Potato"
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Prolatis': Recall - Undeclared Drug Ingredient Sulfoaildenafil
- FDA MedWatch - Lamictal (lamotrigine): Label Change - Risk of Aseptic Meningitis
- Prolatis' Issues a Voluntary Nationwide Recall of its product Prolatis' Marketed as Dietary Supplement prior to August 9, 2010
- From: U.S. Food & Drug Administration (FDA)
- Goya Foods, Inc. Announces Voluntary Recall of Frozen Mamey Pulp
- From: U.S. Food & Drug Administration (FDA)
- Building a healthier America, one community at a time
- FDA: Aseptic Meningitis Risk with Use of Seizure Drug Lamictal
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 11, 2010
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Novacare LLC Products: Recall - Undeclared Drug Ingredient
- WHO Recommendations for the Post-pandemic Period
- From: U.S. Dept. of Health & Human Services
- WHO Director-General Statement
- From: U.S. Dept. of Health & Human Services
- FoodSafety.gov Recall: Fresh Express Veggie Lovers Salad
- Fresh Express Announces Precautionary Recall of a Limited Number of Cases of Veggie Lovers Salad with an Expiration Date of August 10 Due to a Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Ikaria® Recalls INOMAX® DS Drug-Delivery System
- From: U.S. Food & Drug Administration (FDA)
- Novacare LLC Conducts Voluntary Nationwide Recall of Products Found to Contain Undeclared Drug Ingredient
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- U.S. Food & Drug Administration (FDA) CBER's Recalls, Withdrawals, Field Corrections & Notifications Update
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov News & Features Update
- FDA: Salmonella risk from frozen rodents fed to reptiles
- From: U.S. Food & Drug Administration (FDA)
- Questions and Answers: CSL Seasonal Influenza Vaccine Safety in the U.S.
- From: U.S. Dept. of Health & Human Services
- Recommended Flu Vaccines for Different Age Groups
- From: U.S. Dept. of Health & Human Services
- Update of CVM's What's New - FDA warns of Salmonella risk from frozen rodents fed to reptiles
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - August 2010 FDA Patient Safety News now available
- FDA MedWatch - Inferior Vena Cava (IVC) Filters: Initial Communication: Risk of Adverse Events with Long Term Use
- FoodSafety.gov Recalls: Allergy Alert (Chocolate Covered Nuts) and Truffle Puree
- FDA MedWatch - Solo Slim, Solo Slim Extra Strength: Recall - Undeclared Drug Ingredient
- FDA MedWatch - Revivexxx Extra Strength: Recall - Undeclared Drug Ingredient
- The August 2010 FDA Patient Safety News is now available...
- From: U.S. Food & Drug Administration (FDA)
- EZVille, Ltd. Issues a Voluntary Nationwide Recall of Revivexxx® Extra Strength Found to Contain an Undeclared Drug Ingredient
- From: U.S. Food & Drug Administration (FDA)
- EZVille, Ltd. Issues a Voluntary Nationwide Recall of Solo Slim® Found to Contain an undeclared Drug Ingredient
- From: U.S. Food & Drug Administration (FDA)
- South Bend Chocolate Company Announces Nationwide Recall of Bountiful Blend Chocolates Due to Undeclared Tree Nuts
- From: U.S. Food & Drug Administration (FDA)
- FDA Seeks Injunction Against Colorado Manufacturer of Cultured Cell Product
- From: U.S. Food & Drug Administration (FDA)
- WHO Updates International H1N1 Flu Situation
- From: U.S. Dept. of Health & Human Services
- HIV/AIDS Update -Tentative approval of lamivudine and stavudine Fixed Dose Combination tablets
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety Recall: Frozen Ground Beef
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Product Recall - Eugenio Brezzi Truffle Puree
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Guidance for Industry Drug Substance Chemistry, Manufacturing, and Controls Information
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for August 4, 2010
- 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 Color Additive News Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Merrick Pet Care Recalls Texas Hold'ems 10 oz Bag (Item # 60016 Lot 10127 Best by May 6 2012) because of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Merrick Pet Care Recalls Texas Hold'ems 10 oz Bag (Item # 60016 Lot 10127 Best by May 6 2012) because of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Who makes sure the food I buy at the grocery store is safe to eat?
- From: U.S. Food & Drug Administration (FDA)
- Upcoming Webinar Tuesday, August 10th - Using a Food Label to Make Smart Food Choices
- From: U.S. Food & Drug Administration (FDA)
- FDA Issues Assessments of the 510(k) Program and Use of Science in Decision-Making
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Allergy Alert: Canned Meatballs in Sauce Contain Eggs
- Update of CVM's What's New - P&G Expands Voluntary Limited Recall of Specialized Dry Pet Foods Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- P&G Expands Voluntary Limited Recall of Specialized Dry Pet Foods Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- KCB Issues Allergy Alert on Possible Eggs In "KCB No Eggs Added Cake Rusk 28oz"
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Allergy Alert: Eggs in "Cake Rusk"
- Nimodipine Oral Capsules: Medication Errors - IV Administration May Result in Death, Serious Harms
- FDA MedWatch - NeoProfen (ibuprofen lysine) Injection: Recall and Shortage - Risk of Particulate Matter
- STATEMENT BY MARGARET A. HAMBURG, COMMISSIONER OF FOOD AND DRUGS ON THE REOPENING OF SOME MISSISSIPPI STATE WATERS TO COMMERCIAL FISHING
- From: U.S. Food & Drug Administration (FDA)
- STATEMENT BY MARGARET A. HAMBURG, COMMISSIONER OF FOOD AND DRUGS ON THE REOPENING OF FLORIDA STATE WATERS TO COMMERCIAL FISHING
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Announces Draft Compliance Policy Guide: Salmonella in Animal Feed
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Announces FY 2011 Animal Drug/Animal Generic Drug User Fees
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Vaccines for the 2010-2011 Influenza Season
- From: U.S. Dept. of Health & Human Services
- United States Seeks Permanent Injunction Against New York Food Processor
- From: U.S. Food & Drug Administration (FDA)
- Lundbeck Inc. Announces the Voluntary Nationwide Recall of Two Lots of NeoProfen® (ibuprofen lysine) Injection Recall will Result in Temporary Product Shortage
- From: U.S. Food & Drug Administration (FDA)
- Bay Valley Foods Issues Allergy Alert on Undeclared Egg and Wheat in Cans of Mislabeled Chef's Cupboard Chicken with Rice Soup
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Vaccines for the 2010-2011 Influenza Season
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns Consumers of Serious Harm from Drinking Miracle Mineral Solution (MMS)
- From: U.S. Food & Drug Administration (FDA)
- Join us Today at 1:00pm ED for a Special HealthCare.gov Webchat
- FDA MedWatch - Miracle Mineral Solution (MMS): Product as consumed produces a potent bleach that can cause serious harm
- FDA MedWatch - Afluria (CSL Ltd.) Influenza Virus Vaccine: Label Change - Risk of Fever and Febrile Seizure
- FDA MedWatch - Nutraloid Labs ejaculoid XXTREME and stimuloid II: Undeclared Drug Ingredient
- Prevention and Control of Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices (ACIP), 2010
- From: U.S. Dept. of Health & Human Services
- NIAID Grantees Use New Skin Patches to Deliver Flu Vaccine in Mice
- From: U.S. Dept. of Health & Human Services
- The August 2010 MedSun Newsletter is now available...
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Evamist Hormone Spray May Cause Illness in Pets
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Pennsylvania Dairy Farm Agrees to Stop Improper Medication
- From: U.S. Food & Drug Administration (FDA)
- FDA Statement on the Reopening of Some La. State Waters to Commercial Fishing
- From: U.S. Food & Drug Administration (FDA)
- Today: Don Berwick highlights Medicare's 45th Anniversary
- FoodSafety.gov Recall: Organic Alfalfa Sprouts
- Specialty Farms, LLC Expands Recall of Organic Alfalfa Sprouts Blend and Organic Sprout Salad in the North Eastern United States Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Nutraloid Labs Inc. Conducts Voluntary Nationwide Recall of Two Dietary Supplements Found to Contain Undeclared Drug Ingredient
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Evamist (estradiol transdermal spray): Drug Safety Communication - Unintended Exposure of Children and Pets to Topical Estrogen
- FDA Advisory: Avoid Unintentional Exposure of Children and Pets to Evamist
- From: U.S. Food & Drug Administration (FDA)
- Former CEO of Seafood Importing Corporation Sentenced to Federal Prison for Importing Falsely Labeled Fish
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Cubicin (daptomycin): Drug Safety Communication - Risk of Eosinophilic Pneumonia
- Enforcement Report for July 28, 2010
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves Drug for Chronic Drooling in Children
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov News & Events Update
- From: U.S. Dept. of Health & Human Services
- Update of CVM's What's New - Mice Direct Recalls Frozen Reptile Feed Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- New Early Detection System Helps FDA Identify More than 100 Food Safety Problems in First 7 Months
- From: U.S. Food & Drug Administration (FDA)
- Biggers & Callaham, Llc Dba Mice Direct Recalls Frozen Reptile Feed Because Of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Voluntary Recall of PreserVision® Eye Vitamin AREDS 2 Formula in the United States
- From: U.S. Food & Drug Administration (FDA)
- Federal Agents Seize FastSize Extenders and FastSize EQM Erectile Quality Monitors
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- P&G Recalls Two Lots of Prescription Renal Diet Cat Food due to a Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Pennsylvania Dairy Farm Agrees to Stop Improper Medication
- From: U.S. Food & Drug Administration (FDA)
- Airgas South Initiates Precautionary Voluntary Recall of Medical Gas Products at Chattanooga, TN Facility
- From: U.S. Food & Drug Administration (FDA)
- Foodsafety.gov Recall: Corn/Pepper Blend (Chipotle Mexican Grill Restaurant)
- From: U.S. Dept. of Health & Human Services
- Oregon Ice Cream Company Issues Allergy Alert on Undeclared Peanuts in Denali Bear Claw Ice Cream
- From: U.S. Food & Drug Administration (FDA)
- Specialty Farms, LLC Recalls Organic Alfalfa Sprouts Blend and Organic Sprout Salad in the North Eastern United States Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Pasco Processing LLC, Announces Voluntary Product Recall Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves First Generic Enoxaparin Sodium Injection
- 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)
- FoodSafety.gov ALLERGY ALERT: Corn Pasta
- From: U.S. Dept. of Health & Human Services
- FDA Approves First Generic Enoxaparin Sodium Injection to Prevent DVT
- From: U.S. Food & Drug Administration (FDA)
- Cook brand Ciaglia Blue Rhino/Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets/Trays:Recall due to balloon inflation assembly that may not hold air
- Joyful Slim Herb Supplement:Recall-Undeclared Drug Ingredient:Sibutramine and risk of inintended cardiovascular effects
- DeBoles<sup>® </sup> Nutritional Foods, Inc. Voluntarily Recalls One Lot Code of DeBoles<sup>® </sup>Kids Only! Gluten Free Tubettini Corn Pasta Due to the Presence of an Undeclared Allergen, Lot Code 30JUN11D1
- From: U.S. Food & Drug Administration (FDA)
- Federal Government Seizes Cyanide Antidote Kits from California Company
- From: U.S. Food & Drug Administration (FDA)
- J & H Besta Corp. Issues a Voluntary Nationwide Recall of Joyful Slim Herb Supplement Found to Contain an Undeclared Drug Ingredient
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for July 21, 2010
- From: U.S. Food & Drug Administration (FDA)
- Webchat on Health Reform with Secretary Sebelius, MomsRising and Fran Drescher
- Cook Initiates Voluntary Recall of Certain Ciaglia Blue Rhino and Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets and Trays that Contain a Covidien 6PERC or 8PERC Shiley[TM] Tracheostomy Tube
- From: U.S. Food & Drug Administration (FDA)
- Vaccines and Related Biological Products Advisory Committee Update
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- CONSTELLATION Vision System: Recall
- New Diabetes Publications for Women
- From: U.S. Food & Drug Administration (FDA)
- Vialipro Dietary Supplement: Recall-Undeclared Drug Ingredient
- Foodsafety.gov - Recalls: Chicken Nuggets, Herring
- From: U.S. Dept. of Health & Human Services
- Good Health, Inc. Issues a Nationwide Voluntary Recall of Product Marketed as Dietary Supplement
- From: U.S. Food & Drug Administration (FDA)
- NIH Scientists Advance Universal Flu Vaccine
- From: U.S. Dept. of Health & Human Services
- FDA and Other Federal Agencies Collaborate to Improve Chemical Screening
- From: U.S. Food & Drug Administration (FDA)
- New Jersey Woman Sentenced for Committing Insurance Fraud and Selling Prescription Fertility Drugs via the Internet
- From: U.S. Food & Drug Administration (FDA)
- Slim-30 Herb Supplement: Undeclared Drug Ingredient
- D & M Smoked Fish, Inc. Issues an Allert on Uneviscerated Schmaltz Herring
- From: U.S. Food & Drug Administration (FDA)
- J & H Besta Corp. Issues a Voluntary Nationwide Recall of Slim- 30 Herb Supplement Found to Contain an Undeclared Drug Ingredient
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Advair Diskus (fluticasone propionate and salmeterol inhalation powder): Stolen Product Warning
- FDA Warns Consumers, Pharmacists, and Wholesalers Not to Use Stolen Advair Diskus Inhalers
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - The Journey of an Animal Drug through the Approval Process
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov - RECALL: Raw Cat Food
- From: U.S. Dept. of Health & Human Services
- Feline's Pride Expands Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Feline's Pride Expands Nationwide Recall of its Natural Chicken Formula Cat Food Due to Salmonella Contamination
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Angiotensin Receptor Blockers (ARBs): Ongoing Safety Review for Cancer Risk
- June 2010 Drug Safety Labeling Changes: 28 Medical Product Labels with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions
- Fresh Express Announces Recall of Expired Romaine Lettuce Products with Use-By Dates of July 8 to 12 and "S" in the Product Code Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FoodSafety.gov Recall: Fresh Express Romaine Lettuce Products
- From: U.S. Dept. of Health & Human Services
- Diamond Usa Inc. Issues Allergy Alert On Undeclared Sulfites In "Dry Apricot Rolled"
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- ALLERGY ALERTS: Broccoli Raisin Salad, Apricots
- From: U.S. Dept. of Health & Human Services
- Conference call on preventive care in the Affordable Care Act and Women and Prevention
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for July 14, 2010
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Coumadin 1 mg Tablet Blister Packs: Recall
- Bristol-Myers Squibb Initiates a Nationwide Voluntary Recall of Coumadin (R) 1 mg Tablet Blister Packs
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Arava (leflunomide): Boxed Warning- Risk of Severe Liver Injury
- FDA Issues Requirements for Baxter Healthcare Infusion Pump Recall
- From: U.S. Food & Drug Administration (FDA)
- Recalls: Sliced Apples, Protein Powder
- From: U.S. Dept. of Health & Human Services
- FoodSafety.gov News & Events Update
- From: U.S. Dept. of Health & Human Services
- Florida Company Recalls Sliced Apples
- From: U.S. Food & Drug Administration (FDA)
- Spanish: Federal Agents Seize Bee-Shield Hand Sanitizer from Puerto Rican Company
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Air- or Gas-Pressurized Spray Devices: Risk of Air or Gas Embolism
- Federal Agents Seize Bee-Shield Hand Sanitizer from Puerto Rican Company
- From: U.S. Food & Drug Administration (FDA)
- RECALLS: Chile Peppers, Frozen Avocado Pulp
- From: U.S. Dept. of Health & Human Services
- FDA: New Final Rule to Ensure Egg Safety, Reduce Salmonella Illnesses Goes Into Effect
- From: U.S. Food & Drug Administration (FDA)
- HIV/AIDS Update -Tentative approval of fixed dose combination lamivudine, nevirapine, and zidovudine tablets for Oral Solution, 30 mg/50 mg/60 mg)
- From: U.S. Food & Drug Administration (FDA)
- FDA Basic Video: Lawrence Deyton Discusses Tobacco (Video)
- From: U.S. Food & Drug Administration (FDA)
- McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products in the United States, Fiji, Guatemala, Dominican Republic, Puerto Rico, Trinidad & Tobago, and Jamaica
- From: U.S. Food & Drug Administration (FDA)
- Miravalle Foods Inc. Recalls Chile California & Chile Nuevo Mexico Peppers Because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- J. Hellman Frozen Foods, Inc. Recalls Señor Mexicano[TM] Avocado Pulp Due to Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Qualaquin (quinine sulfate): New Risk Management Plan due to potential for serious hematological reactions
- FDA MedWatch - Que She Herbal Supplement: Undeclared drug ingredients could interact with other medications
- Update of CVM's What's New - July 2010 Green Book Monthly Update
- From: U.S. Food & Drug Administration (FDA)
- FDA Public Health Alert: Que She Weight Loss Capsules Contain Potentially Harmful Ingredients
- From: U.S. Food & Drug Administration (FDA)
- CVM Updates - FDA Announces Minor Use/Minor Species Grant Program Request for Applications
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns Consumers, Pharmacists, and Wholesalers Not to Use Stolen Advair Diskus Inhalers
- From: U.S. Food & Drug Administration (FDA)
- FDA Warns of Risks with Unapproved Use of Malaria Drug Qualaquin
- From: U.S. Food & Drug Administration (FDA)
- Ready Pac Foods, Inc. Announces Voluntary Product Recall because of Possible Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- What does 'recall' mean?
- From: U.S. Food & Drug Administration (FDA)
- What products are regulated as electronic products that emit radiation?
- From: U.S. Food & Drug Administration (FDA)
- Enforcement Report for July 7, 2010
- From: U.S. Food & Drug Administration (FDA)
- FDA Seeks Public Comment on New Federal Menu Labeling Requirements
- From: U.S. Food & Drug Administration (FDA)
- FDA Hepatitis Update - Infergen (interferon alfacon-1) label revision: combination therapy, weight-based dosing, and label format
- From: U.S. Food & Drug Administration (FDA)
- Drug Shortages Update
- From: U.S. Food & Drug Administration (FDA)
- Webinar on FDA's Safety Monitoring of Approved Vaccines
- From: U.S. Food & Drug Administration (FDA)
- Recall: Dog Treats (Possible Salmonella)
- From: U.S. Dept. of Health & Human Services
- FDA MedWatch - July 2010 FDA Patient Safety News now available
- The July 2010 FDA Patient Safety News is now available...
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Merrick Pet Care Recalls Beef Filet Squares 10oz Bag (Item #60016 Lot # 10084TL7 Best By March 24, 2012) Because Of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Update of CVM's What's New - Aquaculture Brochure
- From: U.S. Food & Drug Administration (FDA)
- Merrick Pet Care Recalls Beef Filet Squares 10oz Bag (Item #60016 Lot # 10084TL7 Best By March 24, 2012) Because Of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- FDA Approves First Implantable Miniature Telescope to Improve Sight of AMD patients
- From: U.S. Food & Drug Administration (FDA)
- Recalls: Bison/Buffalo Products, Vitamins for Dogs, Energy Mix
- From: U.S. Dept. of Health & Human Services
- Update of CVM's What's New - United Pet Group Voluntarily Expands Recall of Nutritional Supplements For Dogs to Include Additional Tablet and Powdered-Form Products for Dogs and Cats Because of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Undeclared Peanuts and Chocolate Flavored Chips in Select Containers of Fairway "Energy Mix" and Setton Farms "Total Energy Mix"
- From: U.S. Food & Drug Administration (FDA)
- United Pet Group Voluntarily Expands Recall of Nutritional Supplements For Dogs to Include Additional Tablet and Powdered-Form Products for Dogs and Cats Because of Possible Salmonella Health Risk
- From: U.S. Food & Drug Administration (FDA)
- Pharmacy Owner Sentenced to Over 4 Years for Health Care Fraud, Aggravated Identity Theft and Conspiracy to Misbrand Drugs
- From: U.S. Food & Drug Administration (FDA)
- Is FDA responsible for regulating pesticides that are used in animal products?
- From: U.S. Food & Drug Administration (FDA)
- FDA MedWatch - Cepheid Xpert MRSA/SA Blood Culture Assay for Use with the GeneXpert Dx System: Class I Recall
- FDA MedWatch - LIFEPAK 20 and LIFEPAK 20e External Defibrillator/Monitors by Physio-Control Inc.: Class I Recall Due To Power Supply Failure
- Get Food Recalls & Allergy Alerts on Your Smart Phone
- From: U.S. Dept. of Health & Human Services
[Index of Archives]
[CDC News]
[NIH News]
[Epson Inkjet]
[Yosemite]
