FDA News Releases

• Date Index

• FDA inspects retailers in Miss.; issues warning letters for illegal tobacco sales to minors, U.S. Food & Drug Administration (FDA)
• RECALL: Cilantro & Parsley (Wegmans, Boncheff brands) in NY & PA, FoodSafety.gov
• ALLERGY ALERT: Beef, Turkey, and Chicken Tamales in CA, OR, WA, FoodSafety.gov
• Boncheff Greenhouses, Inc. Recalls For Wegmans Food Markets, Inc., Budwey Markets, Wades Market, Cuba Giant Food Market, And Hegedorn's Cilantro, Curly Parsley, And Italian Parsley Because Of A Possible Health Risk., U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of lamivudine and zidovudine tablets, 30 mg/60 mg fixed-dose combination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Triad Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks: Recall Due to Potential Microbial Contamination, FDA MedWatch
• FDA MedWatch - Metronidazole Tablets, 250mg: Recall - Underweight Tablets, FDA MedWatch
• Triad Group Issues a Voluntary Nationwide Recall of All Lots of Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks Due to Potential Microbial Contamination, U.S. Food & Drug Administration (FDA)
• Teva Pharmaceuticals, U.S.A issues a voluntary nationwide recall of Metronidazole Tablets USP, 250mg Due to Low Weight Tablets, U.S. Food & Drug Administration (FDA)
• FDA launches website to help regulated industries save time, resources, U.S. Food & Drug Administration (FDA)
• Enforcement Report for January 5, 2011, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - CVM is now accepting applications for its 2011 Student Summer Intern Program "Windows to Regulatory Research.", U.S. Food & Drug Administration (FDA)
• FDA to require substantial equivalence reviews for new tobacco products, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - AngioScore Inc., AngioSculpt Percutaneous Transluminal Angioplasty (PTA) Scoring Balloon Catheter OTW 0.018" Platform - Class I Recall, FDA MedWatch
• RECALL: Sprouts in WA, OR, ID and AK, FoodSafety.gov
• FDA Basics Webinar: State Enforcement Program, U.S. Food & Drug Administration (FDA)
• The January 2011 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• SPROUTERS NORTHWEST, INC. RECALLS CLOVER SPROUTS AND CLOVER SPROUT MIXES BECAUSE OF POSSIBLE HEALTH RISK, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Sprouters Northwest, Inc. Recalls Clover Sprouts and Clover Sprout Mixes Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA: Don't Eat Certain Lots of Tiny Greens Brand Alfalfa Sprouts or Spicy Sprouts, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA: Don't Eat Certain Lots of Tiny Greens Brand Alfalfa Sprouts or Spicy Sprouts, U.S. Food & Drug Administration (FDA)
• PRock Marketing, LLC Issues a Voluntary Nationwide Recall of All weight loss formulas and variation of formulas of Reduce Weight Fruta Planta/Reduce Weight Dietary Supplement., U.S. Food & Drug Administration (FDA)
• The Ritedose Corporation Announces the Voluntary Nationwide Recall of 0.083% Albuterol Sulfate Inhalation Solution, 3 mL Due to Mislabeled Unit Dose Vials, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Albuterol Sulfate Inhalation Solution 0.083%, 3 mL Unit Dose Vials: Recall - Mislabeled Unit Dose Vials, FDA MedWatch
• CVM Updates - FDA Announces Minor Use and Minor Species (MUMS) Grant Program Request for Applications, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Breaded Chicken Wing Products with Egg Distributed to Restaurants, FoodSafety.gov
• RECALL: Organic Ground Beef Sold in CA, NJ, NY, NC, WI, WA, FoodSafety.gov
• FDA warns consumers not to use Fruta Planta weight loss products, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA warns consumers not to use Fruta Planta weight loss products, U.S. Food & Drug Administration (FDA)
• Drive Total Energy Issues a Voluntary Recall of Rock Hard Extreme and Passion Coffee Dietary Supplements, U.S. Food & Drug Administration (FDA)
• Cumberland Pharmaceuticals Announces Voluntary Recall of Acetadote® Vials, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Acetadote (acetylcysteine) Injection: Recall - Particulate Matter Found in a Small Number of Vials, FDA MedWatch
• ALLERGY ALERT: Cuernos (Croissants), FoodSafety.gov
• ALLERGY ALERT: Teriyaki Beef Jerky with Wheat, FoodSafety.gov
• Recall: Fresh Greens, Herbs, Other Produce, FoodSafety.gov
• Mexicantown Wholesale Issues Allergy Alert For Undeclared Milk in Cuernos (Croissants), U.S. Food & Drug Administration (FDA)
• TINY GREENS ORGANIC FARM FOOD CO. RECALLS PRODUCT BECAUSE OF POSSIBLE HEALTH RISK, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 29, 2010, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Arrow Intra-Aortic Balloon (IAB) Catheter Products: Class 1 Recall - Catheters can become Stuck in the Sheath, FDA MedWatch
• J&D Produce Announces Precautionary, Voluntary Recall Of Fresh Greens, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sodium Bicarbonate Injection, USP, 7.5% and 8.4%, 50 mL Single Dose Vials - Recall Due to Particulates in Some Vials, FDA MedWatch
• ev3 Initiates Voluntary Recall of Specific Lots of NanoCross[TM] .014" OTW PTA Dilatation Catheter, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • ev3 Initiates Voluntary Recall of Specific Lots of NanoCross[TM] .014" OTW PTA Dilatation Catheter, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Nationwide Voluntary Recall of Sodium Bicarbonate Injection, USP 7.5% and 8.4%, 50mL Single Dose Vials Due to Particulate Matter, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • American Regent Initiates Nationwide Voluntary Recall of Sodium Bicarbonate Injection, USP 7.5% and 8.4%, 50mL Single Dose Vials Due to Particulate Matter, U.S. Food & Drug Administration (FDA)
• ev3 NanoCross .014" OTW PTA Dilatation Catheter: Class I Recall - Potential for cracking or breaking, FDA MedWatch
• FDA: Don't Eat Tiny Greens Brand Alfalfa Sprouts or Spicy Sprouts, U.S. Food & Drug Administration (FDA)
• Brand Castle, LLC Issues Allergy Alert On Undeclared Egg In Icing Of Licensed Rice Krispies Treats Holiday Village Kit Distributed Through Michaels Retail Stores Only, U.S. Food & Drug Administration (FDA)
• American Regent Initiates Voluntary Recall of Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL, 30 mL Multiple Dose Vial, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Announces A Recall Of Products Which Were Produced By Rolf's Patisserie In Seven States In The Midwest Because Of A Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Announces A Recall For Ginger Bread Houses Which Were Produced By Rolf's Patisserie In Twenty-Three States Because Of A Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Abbott Diabetes Care Announces Recall of Certain Lots of Precision Xtra®, Precision Xceed Pro®, MediSense® Optium[TM], Optium[TM], OptiumEZ and ReliOn® Ultima Blood Glucose Test Strips in the United States and Puerto Rico, U.S. Food & Drug Administration (FDA)
• JFC International Inc. Recalls "Frozen Capelin" Due To Possible Health Risk, U.S. Food & Drug Administration (FDA)
• South Florida Bakery Issues Recall for Publix Bakery Coconut Macaroons (Coquitos), U.S. Food & Drug Administration (FDA)
• FDA: Rolf's Patisserie recalling all desserts made after November 1, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA: Rolf's Patisserie recalling all desserts made after November 1, U.S. Food & Drug Administration (FDA)
• Dexamethasone Sodium Phosphate Injection, 4 mg/mL, 30 mL Multiple Dose Vial: Recall due to Particulates in Product, FDA MedWatch
• FDA MedWatch - Fruta Planta: Public Notification - Undeclared Drug Ingredient, FDA MedWatch
• FDA MedWatch - RockHard Weekend, Pandora: Recall - Undeclared Drug Ingredient, FDA MedWatch
• HIV/AIDS Update - New Intelence (etravirine) dosage approved, U.S. Food & Drug Administration (FDA)
• Pfizer To Recall One Lot Of Lipitor In The U.S., U.S. Food & Drug Administration (FDA)
• RockHard Laboratories Issues a Voluntary Recall of Specific Lots of the Dietary Supplements RockHard Weekend and Pandora, U.S. Food & Drug Administration (FDA)
• FDA: Gardasil approved to prevent anal cancer, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA: Gardasil approved to prevent anal cancer, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Recombinant Human Growth Hormone (somatropin): Ongoing Safety Review - Possible Increased Risk of Death, FDA MedWatch
• Shining a Light on Insurance Companies, HealthCare.gov
• FDA announces recall of Abbott glucose test strips, U.S. Food & Drug Administration (FDA)
• RECALLS: Frozen capelin fish and, FoodSafety.gov
• FDA MedWatch - Abbott Glucose Test Strips: Recall - False Low Blood Glucose Results, FDA MedWatch
• IMPF Voluntarily Recalls Dips & Spreads because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 22, 2010, U.S. Food & Drug Administration (FDA)
• Secretary of Health and Human Services Announces 2011 Healthy Living Innovation Awards, U.S. Food & Drug Administration (FDA)
• Whole Foods Market Announces Cheese Recall For Products In Three Western States And Washington, D.C. Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• JFC International Inc Issues An Alert On Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fresenius Kabi LLC, Red Blood Cell (RBC) Exchange Sets used on AS104 Blood Cell Separation Devices: Class I Recall, FDA MedWatch
• HHS and Walgreens Announce New Effort Aimed at Addressing Health Disparities in Flu Vaccination, U.S. Dept. of Health & Human Services
• Kroger Recalls Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• YNOT FOODS INC. Issues Allergy Alert on Undeclared Milk and Soybean in Upsides[TM] Orzo Toscano, 6/2.5lb, U.S. Food & Drug Administration (FDA)
• Tofutti Brands Inc. Announces Updated Information for Recall of 25 Pallets of Yours Truly Frozen Dessert Cones Due to Possible Trace Level Milk Contamination, U.S. Food & Drug Administration (FDA)
• U.S. Food & Drug Administration (FDA) BadAd Update, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Kroger Recalls Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - NARMS Retail Meat Annual Report, 2008, U.S. Food & Drug Administration (FDA)
• FDA: Consumers should not eat Sally Jackson cheese due to risk of Escherichia coli O157:H7, U.S. Food & Drug Administration (FDA)
• RECALL: All Sally Jackson Cheese, FoodSafety.gov
• FDA MedWatch - Anzemet (dolasetron mesylate): Drug Safety Communication - Reports of Abnormal Heart Rhythms, FDA MedWatch
• Sally Jackson Cheese Recalls All Cheese Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Avastin (bevacizumab): Process for Removal of Breast Cancer Indication Begun, FDA MedWatch
• FDA Hepatitis Update - New Guidance for Industry: Codevelopment of Two or More Unmarketed Investigational Drugs for Use in Combination, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - New Guidance for Industry: Codevelopment of Two or More Unmarketed Investigational Drugs for Use in Combination, U.S. Food & Drug Administration (FDA)
• FDA begins process to remove breast cancer indication from Avastin label, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - New Issue of FDA Veterinarian Newsletter!, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 15, 2010, U.S. Food & Drug Administration (FDA)
• FDA: Tainted products marketed as dietary supplements potentially dangerous, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Brinkman's Gourmet Barbecue Sauce, FoodSafety.gov
• Update of CVM's What's New - December 2010 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• Brinkman Turkey Farms Inc. Issues Allergy Alert On Undeclared Soy And Milk In "Brinkman's Gourmet Barbecue Sauce"., U.S. Food & Drug Administration (FDA)
• FDA says Tessalon liquid cough capsules pose risk for young children, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tessalon (benzonatate): Drug Safety Communication - Potential for Accidental Ingestion by Children, FDA MedWatch
• FDA MedWatch - Rolaids Extra Strength Softchews, Rolaids Extra Strength plus Gas Softchews, Rolaids Multi-Symptom plus Anti-Gas Softchews: Recall - Foreign Materials in Products, FDA MedWatch
• Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Minor Use/Minor Species Drug Designations List, U.S. Food & Drug Administration (FDA)
• RECALL: Walnuts with Salmonella, FoodSafety.gov
• H1N1 Vaccine Safe and Induces Robust Immune Response in People with Asthma, U.S. Dept. of Health & Human Services
• U.S. Food & Drug Administration (FDA) New FDA Basics Summary Metrics, U.S. Food & Drug Administration (FDA)
• Tropical Nut & Fruit of Charlotte, NC Announces a Nationwide Voluntary Recall of Walnut Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• McNeil Consumer Healthcare Announces Voluntary Recall Of All Lots Of Rolaids® Extra Strength Softchews, Roldaids® Extra Strength Plus Gas Softchews, And Roldaids® Multi-Symptom Plus Anti-Gas Softchews Sold In The United States, U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize FDA-regulated food stored at rodent-infested warehouse in New Mexico, U.S. Food & Drug Administration (FDA)
• Updated: With Table - Reese Pharmaceutical Company Announces the Voluntary Nationwide Recall of Certain Over-The-Counter Cold Relief Products that are Mislabeled., U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - New labeling approved for Prezista (darunavir), U.S. Food & Drug Administration (FDA)
• Toffutti Brands Inc. Announces Recall Of 25 Pallets Of Yours Truly Frozen Dessert Cones Due To Possible Trace Level Milk Contamination, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Man Up Now Capsules: Consumer Warning - Undeclared Drug Ingredient, FDA MedWatch
• ALLERGY ALERT: Sauteed Chicken Products Sold to Restaurants in CA and HI, FoodSafety.gov
• FDA MedWatch - Reese Pharmaceutical Company OTC Products: Recall - Mislabeled Guaifenesin Tablets, FDA MedWatch
• Reese Pharmaceutical Company Announces the Voluntary Nationwide Recall of Certain Over-The-Counter Cold Relief Products that are Mislabeled., U.S. Food & Drug Administration (FDA)
• FDA warns consumers to avoid Man Up Now capsules, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update -New labeling for Zerit capsules and Zerit for oral solution, U.S. Food & Drug Administration (FDA)
• Mojave Foods Corporation Initiates Recall Due to Possible Health Risk from Walnut Ingredient, U.S. Food & Drug Administration (FDA)
• CVM Updates - CVM Reports on Antimicrobials Sold or Distributed for Food-Producing Animals, U.S. Food & Drug Administration (FDA)
• RECALLS: Cilantro, Pork Products, Dried Fish, FoodSafety.gov
• FDA issues guidance on public comment procedures at advisory committee meetings, U.S. Food & Drug Administration (FDA)
• Pablo's Produce, Inc. Recalls One Lot of Cilantro because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 8, 2010, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Penumbra System Reperfusion Catheter 032: Class I Recall Due to Manufacturing Error, FDA MedWatch
• November 2010 Safety Labeling Changes: 37 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• A Flu Vaccine that Lasts: NIH Scientists Consider Prospects for a Universal Influenza Vaccine, U.S. Dept. of Health & Human Services
• Presidential Proclamation--National Influenza Vaccination Week, U.S. Dept. of Health & Human Services
• S&S Food Inc. Issues An Alert On Uneviscerated Fish, U.S. Food & Drug Administration (FDA)
• The December 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
• Wisconsin Business Recalls Smoked Fish Spread; May Be Contaminated With Listeria, U.S. Food & Drug Administration (FDA)
• National Influenza Vaccination Week to be held December 5-11, 2010, U.S. Dept. of Health & Human Services
• Seasonal Flu and 2009 H1N1 Flu Vaccination Coverage Among Pregnant Women, 2009--10 Flu Season, U.S. Dept. of Health & Human Services
• Lobby Shoppes, Inc. Issues An Allergy Alert On Milk And Soy Products In "Cheese Popcorn, Chicago Triple Mix Popcorn And Caramel Corn", U.S. Food & Drug Administration (FDA)
• California Firm Recalls Chicken Tamales Due To Mislabeling and an Undeclared Allergen, FoodSafety.gov
• RECALL: Bumble Bee Chicken Salad, FoodSafety.gov
• Intelli Health Products, Issues an Expansion to All Lots of their Voluntary Nationwide Recall of Duro Extend Capsules for Men Marketed as Dietary Supplements, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - FDA seeking new members with Hep C experience for its Antiviral Drugs Advisory Committee, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Approves First Drug to Prevent Life Threatening Disease in Horses, U.S. Food & Drug Administration (FDA)
• RECALL: NY Gourmet Salads, FoodSafety.gov
• Update of CVM's What's New - New Guidance - Residual Solvents in Animal Drug Products, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of rapid INSTI[TM] HIV-1 Antibody Test, U.S. Food & Drug Administration (FDA)
• Recall of Mylanta and Alternagel Liquid Products, U.S. Food & Drug Administration (FDA)
• Special Edition OWH eUpdate, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - November 2010 Green Book Update, U.S. Food & Drug Administration (FDA)
• RECALL: Frontier and Whole Foods Nutmeg, FoodSafety.gov
• Frontier Natural Products Co-op Initiates Voluntary Recall Due to Possible Health Risk from Nutmeg, U.S. Food & Drug Administration (FDA)
• Enforcement Report for December 1, 2010, U.S. Food & Drug Administration (FDA)
• B. Braun addEASE Binary Connector: Class I Recall -Stopper Fragments May Enter Bag, FDA MedWatch
• ALLERGY ALERT: Golden Dipt® Fry Easy All-Purpose Batter, FoodSafety.gov
• The December 2010 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• McCormick & Company Recalls Golden Dipt® Fry Easy All-Purpose Batter Due To Unlabeled Egg Ingredient, U.S. Food & Drug Administration (FDA)
• FDA Permits Wright County Egg to begin shipping shell eggs to consumers, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of abacavir sulfate tablets, 60 mg, U.S. Food & Drug Administration (FDA)
• FDA Office of Minority Health Website is live, U.S. Food & Drug Administration (FDA)
• Recall of ROLAIDS® Extra Strength Softchews, U.S. Food & Drug Administration (FDA)
• Recall of Tylenol Cold Liquid Products, U.S. Food & Drug Administration (FDA)
• Recall of Children's BENADRYL&#174; Allergy FASTMELT&#174; Tablets and Junior Strength MOTRIN&#174; Caplets, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - HiRes 90K Cochlear Implant Device: Recall - Malfunction, FDA MedWatch
• Advanced Bionics Announces Voluntary Recall Of The Hires 90k Cochlear Implant, U.S. Food & Drug Administration (FDA)
• Bravo Farms announces cheese recall, some products sold under Whole Foods Market label in 5 Western states, U.S. Food & Drug Administration (FDA)
• WalkMed Infusion Issues Nationwide Recall of Triton Pole Mount Infusion Pumps, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 24, 2010, U.S. Food & Drug Administration (FDA)
• RECALL: Organic Dark Chocolate Squares, FoodSafety.gov
• RECALL: Bravo Farms Recalls All Cheese, FoodSafety.gov
• Bravo Farms Cheese Recall, U.S. Food & Drug Administration (FDA)
• Artisan Confections Recalls Dagoba new moon&#8482; Rich Dark Chocolate 74% Cacao 0.32-Ounce Squares Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Minor Use Minor Species Designations List, U.S. Food & Drug Administration (FDA)
• FDA Basics Webinar: Melamine: The Cause of the Pet Food and Infant Formula Recalls, 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, 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, FDA MedWatch
• KRUNCHERS! INC. RECALLS 18 CASES OF JAYS ORIGINAL POTATO CHIPS BECAUSE OF UNDECLARED MILK ALLERGEN, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Krunchers! Inc. Recalls 18 Cases Of Jays Original Potato Chips Because Of Undeclared Milk Allergen, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Vigor-25: Undeclared Drug Ingredient - Sold as Natural Dietary Supplement, FDA MedWatch
• FDA warns consumers not to use Vigor-25, U.S. Food & Drug Administration (FDA)
• Interim Guidance on the Use of Influenza Antiviral Agents During the 2010-2011 Influenza Season, U.S. Dept. of Health & Human Services
• FDA MedWatch - Propoxyphene: Withdrawal - Risk of Cardiac Toxicity, FDA MedWatch
• Xanodyne agrees to withdraw propoxyphene from the U.S. market, U.S. Food & Drug Administration (FDA)
• FDA approves Xgeva to help prevent cancer-related bone injury, U.S. Food & Drug Administration (FDA)
• NIH Experts Describe Influenza Vaccines of the Future, U.S. Dept. of Health & Human Services
• Enforcement Report for November 17, 2010, U.S. Food & Drug Administration (FDA)
• The Great American Smokeout, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Needleless Pre-filled Glass Syringes: Stakeholder Advisory - Compatibility Problems with Needleless Intravenous Access Systems, FDA MedWatch
• Del Bueno Recalls Cheese Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA Warning Letters issued to four makers of caffeinated alcoholic beverages, U.S. Food & Drug Administration (FDA)
• Liz Lovely Issues Voluntary Recall on Products Containing Chocolate Due to Undeclared Dairy from Chocolate Supplier, U.S. Food & Drug Administration (FDA)
• Allergy Alert: Dried Taro with Sulfites, FoodSafety.gov
• NIH Scientists Explore 1510 Influenza Pandemic and Lessons Learned, U.S. Dept. of Health & Human Services
• S&M (U.S.A) Enterprise Corp Issues Alert on Undeclared Sulfites in Grow Grove Notes Brand Dried Taro, U.S. Food & Drug Administration (FDA)
• FDA launches initiative to develop innovative external defibrillators, U.S. Food & Drug Administration (FDA)
• FDA approves new treatment option for late-stage breast cancer, U.S. Food & Drug Administration (FDA)
• FDA Urges Consumers to be 'Smart' about Antibiotic Use, U.S. Food & Drug Administration (FDA)
• RECALL: Costco Cheese Recalls, FoodSafety.gov
• RECALL: Smoked Turkey Breast Products, FoodSafety.gov
• Voluntary Recall of Bravo Farms Dutch Style Gouda Cheese Due to Health Risk, U.S. Food & Drug Administration (FDA)
• Gorgonzola Cheese Sold at Costco Recalled Due to Contamination With E.coli O157:H7, U.S. Food & Drug Administration (FDA)
• DPI Specialty Foods Recalls Mauri Brand Gorgonzola Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Sigma Spectrum Infusion Pump Model 35700: Class 1 Recall: Risk of Over-Infusion, FDA MedWatch
• October 2010 Safety Labeling Changes: 34 Medical Product Labels with changes to Boxed Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• RECALL: Mauri Gorgonzola cheese sold at Costco in Colorado, FoodSafety.gov
• Enforcement Report for November 10, 2010, U.S. Food & Drug Administration (FDA)
• FDA: Lot of Mauri Gorgonzola cheese positive for E. coli 0157:H7, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA: Lot of Mauri Gorgonzola cheese positive for E. coli 0157:H7, U.S. Food & Drug Administration (FDA)
• FDA Approves Egrifta to Treat Lipodystrophy in HIV Patients, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval of Egrifta to treat lipodystrophy, U.S. Food & Drug Administration (FDA)
• Pharmaceutical Company Lawyer Charged with Obstruction and Making False Statements, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - VITEK 2 Gram Negative Susceptibility Cards Containing Piperacillin/Tazobactam (TZP): Recall - Incorrect Test Results Observed, FDA MedWatch
• FDA: Majority of drug and biological product makers meeting postmarketing requirements and commitments, U.S. Food & Drug Administration (FDA)
• Cal-Maine Foods. Inc. Updates Voluntary Egg Recalls Information, U.S. Food & Drug Administration (FDA)
• FDA working to prevent radiation overdoses during CT scans, U.S. Food & Drug Administration (FDA)
• Allergy Alert: Fresh & Easy Ginger Spice Cookie Dough, FoodSafety.gov
• RECALL: Eggs, FoodSafety.gov
• RECALL: Products Containing Cilantro, FoodSafety.gov
• RECALL: Trader Joe's Chicken Pasta Salad, FoodSafety.gov
• RECALL: Apple Cider, FoodSafety.gov
• Update of CVM's What's New - Registration delayed until November 10: AAVPT Veterinary Drug Regulatory Life Cycle Course, U.S. Food & Drug Administration (FDA)
• HRSA and FDA Present Health Education Awards, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Triton Pole Mount Infusion Pump by WalkMed: Recall - Potential Door Open Alarm Problem, FDA MedWatch
• Cal-Maine Foods, Inc. Conducts Voluntary Egg Recall, U.S. Food & Drug Administration (FDA)
• Orval Kent Food Company, Inc Voluntarily Recalls Products Containing Cilantro Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• WalkMed Infusion Issues Nationwide Recall of Triton Infusion Pump, U.S. Food & Drug Administration (FDA)
• Baugher Enterprise, Inc. Recalls Baugher's Apple Cider Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Carefusion Recall of Alaris PC Units Model 8015 Classified as Class I Recall, U.S. Food & Drug Administration (FDA)
• FDA, State of Maryland, and Baugher Enterprise warn consumers to avoid Baugher's Apple Cider, U.S. Food & Drug Administration (FDA)
• RECALLS: Meat and Poultry Products in Illinois and New York, FoodSafety.gov
• RECALL: Unpasteurized Apple Cider, FoodSafety.gov
• The November 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
• DHMH Issues Consumer Alert Regarding Recall of Baugher's Apple Cider, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Registration Opens November 8: AAVPT Veterinary Drug Regulatory Life Cycle Course, U.S. Food & Drug Administration (FDA)
• FDA, CDC, and Costco warn consumers to avoid Bravo Farms Dutch Style Gouda cheese, U.S. Food & Drug Administration (FDA)
• FDA clears Cymbalta to treat chronic musculoskeletal pain, U.S. Food & Drug Administration (FDA)
• ALERT: FDA, CDC, and Costco warn consumers to avoid Bravo Farms Dutch Style Gouda cheese, FoodSafety.gov
• FDA MedWatch - Hospira Symbiq One-Channel and Two-Channel Infusers: Class I Recall - Motor Encoder Failures, FDA MedWatch
• Beaver Street Fisheries, Inc Voluntarily Recalls Tuna due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Actavis Encourages Consumers to Return Fentanyl Transdermal System 25 mcg/h, U.S. Food & Drug Administration (FDA)
• Intelli Health Products, Issues a Voluntary Nationwide Recall of Duro Extend Capsules for Men Marketed as Dietary Supplements, U.S. Food & Drug Administration (FDA)
• FDA, USDA, Cornell University announce alliance for produce safety, U.S. Food & Drug Administration (FDA)
• FDA reclassifies certain digital mammography devices today, U.S. Food & Drug Administration (FDA)
• Enforcement Report for November 3, 2010, U.S. Food & Drug Administration (FDA)
• New Study Re-examines Bacterial Vaccine Studies Conducted During 1918 Influenza Pandemic, U.S. Dept. of Health & Human Services
• MedSun Update, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - October 2010 Green Book Monthly Update, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Octopus Nuvo Tissue Stabilizer: Recall - Potential for Device Fracture, FDA MedWatch
• FDA Classifies Previous Field Action of Medtronic Surgical Device as Class I Recall, U.S. Food & Drug Administration (FDA)
• FDA, University of Rochester announce partnership for new drug products, U.S. Food & Drug Administration (FDA)
• FDA approves new indication for Afinitor, U.S. Food & Drug Administration (FDA)
• New Video for Women with Diabetes, U.S. Food & Drug Administration (FDA)
• Kosher First LLC. Issues Alert on Listeria in Tuv Taam Salads Nova Lox Salad, U.S. Food & Drug Administration (FDA)
• FDA Approves Teflaro for Bacterial Infections, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Heparin Sodium (B. Braun): Recall - Trace Contaminant, FDA MedWatch
• B. Braun Voluntarily Recalls Seven Lots of Heparin Manufactured in 2008 Due to Supplier-Initiated Recall of Heparin Active Pharmaceutical Ingredient (API), U.S. Food & Drug Administration (FDA)
• NOAA and FDA Announce Chemical Test for Dispersant in Gulf Seafood;, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Methotrexate Injection, 50mg/2mL and 250mg/10mL Vials: Recall - Presence of Glass Particulates, FDA MedWatch
• FDA approves Latuda to treat schizophrenia in adults, 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, U.S. Food & Drug Administration (FDA)
• FDA approves additional medical indication for Sprycel, U.S. Food & Drug Administration (FDA)
• RECALL: Autentico Pork Skins & Pork Products in CA, FoodSafety.gov
• Enforcement Report for October 27, 2010, U.S. Food & Drug Administration (FDA)
• bioMérieux, Inc. Issues Urgent Product Correction for VITEK® 2 Gram Negative Susceptibility Cards Containing Piperacillin/Tazobactam, U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize FDA-regulated food stored at rodent-infested warehouse in Georgia, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Addition of Boxed Warning to METACAM® (meloxicam) Labels, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Safe Animal Feed Video Available, U.S. Food & Drug Administration (FDA)
• FDA awards $18.5 million in grants for food and feed safety, U.S. Food & Drug Administration (FDA)
• Federal government takes action against Tennessee food distributor, U.S. Food & Drug Administration (FDA)
• Federal Government has seized Tri-Med Labs drug products, 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, U.S. Food & Drug Administration (FDA)
• FDA laboratory receives accreditation, U.S. Food & Drug Administration (FDA)
• RECALL: Tomi Dried Seafood Products, Botulism Risk, FoodSafety.gov
• ALLERGY ALERT: Nestle Raisinets, FoodSafety.gov
• RECALL: Market Pantry Beef Sticks, FoodSafety.gov
• Mega Pops Manufacturer Leads Effort with Retailers to Recall Product Voluntarily During Review of Customer Concerns, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Mega Pops Manufacturer Leads Effort with Retailers to Recall Product Voluntarily During Review of Customer Concerns, FoodSafety.gov
• Working with FDA, Standard Homeopathic Company Voluntarily Recalls Hyland's Teething Tablets to Address Manufacturing Process, U.S. Food & Drug Administration (FDA)
• Nestle® USA Issues Allergen Alert on Single Production Code of Nestle® Raisinets® Fun Size Bags, U.S. Food & Drug Administration (FDA)
• DSHS Orders Sangar Produce to Close, Recall Products, U.S. Food & Drug Administration (FDA)
• Hyland's Teething Tablets may pose a risk to children, 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, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Hyland's Teething Tablets: Recall - Risk of Harm to Children, FDA MedWatch
• HIV/AIDS Update - Invirase (saquinavir) labels updated with important risk information about abnormal heart rhythms, U.S. Food & Drug Administration (FDA)
• 2010-2011 Seasonal Influenza (Flu) Vaccine Safety, 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, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Fentanyl Transdermal System: Recall - Potential for Active Ingredient to Release Faster Than Specified, FDA MedWatch
• FDA Heightens Focus on Retail Food Safety, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA heightens focus on retail food safety, U.S. Food & Drug Administration (FDA)
• Foremost Foods International, Inc. Issues Recall on Certain Tomi Dried Seafood Products, U.S. Food & Drug Administration (FDA)
• Actavis Inc. Issues a Voluntary Recall of 18 Lots of Fentanyl Transdermal System 25 mcg/h, U.S. Food & Drug Administration (FDA)
• Del Monte Fresh Produce N.A., Inc. Announces Limited Voluntary Cantaloupe Recall In And Around Detroit, Michigan, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Del Monte Fresh Produce N.A., Inc. Announces Limited Voluntary Cantaloupe Recall In And Around Detroit, Michigan, FoodSafety.gov
• FDA MedWatch - Invirase (saquinavir): Label Change - Risk of Abnormal Heart Rhythm, FDA MedWatch
• New Label Changes for Commonly Prescribed HIV Drug Invirase, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - additional Veterinary Medicine Advisory Committee materials posted, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 20, 2010, U.S. Food & Drug Administration (FDA)
• September 2010 Safety Labeling Changes: 37 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
  • Medicines in My Home Update, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - GnRH Agonists: Label Change - Increased Risk of Diabetes and Cardiovascular Disease (Update), FDA MedWatch
• FDA: Include warnings on risk for class of prostate cancer drugs, U.S. Food & Drug Administration (FDA)
• FDA approves Pradaxa to prevent stroke in people with atrial fibrillation, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update -Tentative approval of lamivudine and stavudine Fixed Dose Combination tablets, 150/300 mg, U.S. Food & Drug Administration (FDA)
• FDA Basics Webinar: Food Emergency Response Network (FERN), U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tylenol 8 Hour Caplets 50 Count: Recall - Uncharacteristic musty or moldy odor, FDA MedWatch
• 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, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Presentations from the September 20, 2010 Veterinary Medicine Advisory Committee Meeting, U.S. Food & Drug Administration (FDA)
• FDA Provides Update on LASIK Quality of Life Collaboration Project Status, U.S. Food & Drug Administration (FDA)
• FDA Authorizes Hillandale Farms to Begin Shipping Fresh Shell Eggs, U.S. Food & Drug Administration (FDA)
• FDA Issues Warning Letter to Wright County Egg, 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, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Pre-Registration Notice: AAVPT Veterinary Drug Regulatory Life Cycle Course, 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, U.S. Food & Drug Administration (FDA)
• RECALL: Frozen Green Pea Products Sold at Kroger & Walmart, FoodSafety.gov
• The Pictsweet Company Announces a Voluntary Recall of Frozen Green Peas Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA approves Botox to treat chronic migraine, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • FDA approves Botox to treat chronic migraine, 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
• FDA MedWatch - CareFusion Corporation Alaris PC Units (Model 8015): Recall - Potential for Delay or Interruption of Therapy, FDA MedWatch
• ALLERGY ALERT: Breaded Okra, FoodSafety.gov
  • <Possible follow-ups>
  • ALLERGY ALERT: Breaded Okra, FoodSafety.gov
• CVM Updates - FDA Announces Letter to Industry on Marketing of Animal Food Substances as Generally Recognized As Safe (GRAS), U.S. Food & Drug Administration (FDA)
• The Pictsweet Company Issues Allergy Alert On Undeclared Milk In 32 Ounce Clear Bag Breaded Okra, 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, U.S. Food & Drug Administration (FDA)
• FDA participates in 'International Internet Week of Action', U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Chelation Products: Unapproved Over-the-Counter Drugs - Consumer Warning, FDA MedWatch
• FDA Determines Knee Device Should Not Have Been Cleared for Marketing, U.S. Food & Drug Administration (FDA)
• FDA issues warnings to marketers of unapproved 'chelation' products, U.S. Food & Drug Administration (FDA)
• Government takes action against Montana drug manufacturer, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Cumulative Veterinary Adverse Drug Experience (ADE) Reports - Updated September 30, 2010, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 13, 2010, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Bisphosphonates (Osteoporosis Drugs): Label Change - Atypical Fractures Update, FDA MedWatch
• FDA: Possible increased risk of thigh bone fracture with bisphosphonates, U.S. Food & Drug Administration (FDA)
• FDA schedules third orphan drug workshop for Nov. 4-5, 2010, U.S. Food & Drug Administration (FDA)
• FDA approves injectable drug to treat opioid-dependent patients, U.S. Food & Drug Administration (FDA)
• RECALL: BLUE brand dog food, FoodSafety.gov
• RECALL: "La Nuestra" Mamey Ice Cream, FoodSafety.gov
• 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, U.S. Food & Drug Administration (FDA)
• LIPITOR Recall Information, 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, U.S. Food & Drug Administration (FDA)
• Influenza Activity - United States and Worldwide, June 13--September 25, 2010, U.S. Dept. of Health & Human Services
• Influenza Vaccination Coverage among Children Aged 6-23 Months - U.S., 2008-09 Influenza Season, U.S. Dept. of Health & Human Services
• Seasonal Flu Information for Businesses and Employees, 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, U.S. Dept. of Health & Human Services
• RECALL: Smoked Fish, FoodSafety.gov
• Montalvan's Sales, Inc. Recalls "La Nuestra" Brand Mamey Ice Cream Because of Potential Health Risk, 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, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Slimming Beauty Bitter Orange Slimming Capsules: Undeclared Drug Ingredient, FDA MedWatch
• FDA MedWatch - Meridia (sibutramine): Market Withdrawal Due to Risk of Serious Cardiovascular Events, FDA MedWatch
• Abbott Laboratories agrees to withdraw its obesity drug Meridia, U.S. Food & Drug Administration (FDA)
• FDA: Potentially harmful stimulant found in Slimming Beauty capsules, 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, U.S. Food & Drug Administration (FDA)
• Living Foods Inc. Initiates a Voluntary Market Withdrawal of Alfalfa Sprouts Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• RECALL: Alfalfa Sprouts, FoodSafety.gov
  • <Possible follow-ups>
  • Recall: Alfalfa Sprouts, FoodSafety.gov
  • RECALL: Alfalfa Sprouts, FoodSafety.gov
• FDA seeks to stop juice company's processing, distribution, U.S. Food & Drug Administration (FDA)
• Enforcement Report for October 6, 2010, U.S. Food & Drug Administration (FDA)
• FDA awards $904,000 to Pan American Health Organization for information 'hub', U.S. Food & Drug Administration (FDA)
• FDA Issues Regulatory Science Report, U.S. Food & Drug Administration (FDA)
• FDA Basic Video: Margaret Oeller (Video), U.S. Food & Drug Administration (FDA)
• How does FDA plan to enforce the restrictions on promotion and advertising established by the Tobacco Control Act?, U.S. Food & Drug Administration (FDA)
• FDA Basic Video: Diane Murphy Discusses Vaccines (Video), U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: White bread with nuts not listed on the label, FoodSafety.gov
• Learn More about New Health Care Benefits - HealthCare.Gov, 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, U.S. Food & Drug Administration (FDA)
• FDA Hepatitis Update - Approval Pathway for Biosimilar and Interchangeable Biological Products Public Meeting Nov. 2-3, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Approval Pathway for Biosimilar and Interchangeable Biological Products, FDA Public Meeting, U.S. Food & Drug Administration (FDA)
• FDA awards nearly $3 million for TB research, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - FDA's Animal Feed Safety System (AFSS) Project Plans Update #7, U.S. Food & Drug Administration (FDA)
• The October 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
• Q and A: Vaccine Selection for the 2010-2011 Influenza Season, U.S. Dept. of Health & Human Services
• FDA schedules public hearing on Biologics Price Competition and Innovation Act, U.S. Food & Drug Administration (FDA)
• Rising Dough Bakery Issues Allergy Alert on Undeclared Walnuts in the Rising Dough Brand Individual Wrapped Cranberry Muffins, U.S. Food & Drug Administration (FDA)
• Insurer Pricing and Denial Rates Now on HealthCare.gov, HealthCare.gov
• HIV/AIDS Update - Tentative approval of abacavir sulfate tablets, 300 mg, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Hostess® Mini Muffins (Chocolate Chip variety), FoodSafety.gov
• CVM Updates - CVM Announces Availability of Online Pet Pharmacy Brochure through Pueblo, Colorado, U.S. Food & Drug Administration (FDA)
• Hostess Brands, Inc. Issues Voluntary Recall of Hostess® Mini Muffins (Chocolate Chip variety) Due to Unlabeled Allergen, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Hostess Brands, Inc. Issues Voluntary Recall of Hostess® Mini Muffins (Chocolate Chip variety) Due to Unlabeled Allergen, U.S. Food & Drug Administration (FDA)
• FDA Orders Halt to Marketing of Unapproved Single-Ingredient Oral Colchicine, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 29, 2010, U.S. Food & Drug Administration (FDA)
• BARDA Funds Development of Next-Generation Portable Ventilators, U.S. Dept. of Health & Human Services
• The October 2010 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Health Requirements and Recommendations for Travel to Saudi Arabia During the 2010 Hajj: Information for U.S. Travelers, U.S. Dept. of Health & Human Services
• FDA MedWatch - Infant sleep positioners: Consumer Warning - Risk of Suffocation, FDA MedWatch
• Deaths prompt CPSC, FDA warning on infant sleep positioners, U.S. Food & Drug Administration (FDA)
• Pfizer Consumer Healthcare Issues Voluntary Recall of One Lot of ThermaCare HeatWraps Menstrual Product, U.S. Food & Drug Administration (FDA)
• FDA Warns three companies to stop making unproven claims on mouth rinses, U.S. Food & Drug Administration (FDA)
• NIH and FDA announce awards to advance regulatory science, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERTS: Granola Thins, Butter Cup Cakes, Pork Ginger Sausage, FoodSafety.gov
• FDA issues final rule on safety information during clinical trials, U.S. Food & Drug Administration (FDA)
• HealthCare.gov on Facebook, HealthCare.gov
• Amgen Initiates Voluntary Nationwide Recall Of Certain Lots Of Epogen® And Procrit® (Epoetin Alfa), U.S. Food & Drug Administration (FDA)
• FDA approves combination contraceptive containing a folate, U.S. Food & Drug Administration (FDA)
• Similac Powder Infant Formulas: Recall-UPDATE: new searchable database and consumer update added, FDA MedWatch
• FDA MedWatch - Octagam (Immune Globulin Intravenous (human)) 5% Liquid Preparation: Market Withdrawal - Risk of Thromboembolic Events, FDA MedWatch
• FDA MedWatch - Epogen and Procrit (epoetin alfa): Recall - Particulate Matter in Vials, FDA MedWatch
• FDA MedWatch - Electric Dental Handpieces and Electric Oral Bone-cutting Handpieces: Safety Investigation of Patient Burns, FDA MedWatch
• Enforcement Report for September 22, 2010, U.S. Food & Drug Administration (FDA)
• Similac Infant Formula: Get a Complete List of Products Recalled, FoodSafety.gov
• CVM Updates - FDA to hold Public Workshop for Animal Health Industry on Release of Beta-Version of eSubmitter, an Electronic Submission Tool, U.S. Food & Drug Administration (FDA)
• Red Lotus Bakery Issues Allergy Alert On Undeclared Eggs In "Butter Cup Cakes", 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, U.S. Food & Drug Administration (FDA)
• Six Months of the Affordable Care Act, HealthCare.gov
• FDA MedWatch - Avandia (rosiglitazone): REMS - Risk of Cardiovascular Events, FDA MedWatch
• FDA significantly restricts access to the diabetes drug Avandia, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Western Family Maple Nut Ice Cream, FoodSafety.gov
• FDA MedWatch - Similac Powder Infant Formulas: Recall, FDA MedWatch
• RECALL: Similac Powder Infant Formula, FoodSafety.gov
• Deluxe Ice Cream Issues Allergy Alert on Undeclared Peanuts in Western Family Maple Nut Ice Cream, U.S. Food & Drug Administration (FDA)
• Suzipoo Issues Allergy Alert on Undeclared Allergen in Lobster Poo, U.S. Food & Drug Administration (FDA)
• Abbott Voluntarily Recalls Certain Similac® Brand Powder Infant Formulas That Did Not Meet Its Quality Standards, U.S. Food & Drug Administration (FDA)
• ALLERGY ALERT: Garvi Gujarat brand Tam Tam (star noodle snack), FoodSafety.gov
• House of Spices Issues Allergy Alert On Undeclared Peanuts in Garvi Gujarat Brand Tam Tam (Star Noodles) 10 oz., U.S. Food & Drug Administration (FDA)
• NIH study models H1N1 flu spread, U.S. Dept. of Health & Human Services
• FDA approves first oral drug to reduce MS relapses, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - CVM Annual Report for Fiscal Year 2009, U.S. Food & Drug Administration (FDA)
• CVM Updates - FDA Announces Minor Use/Minor Species Grant Program Awards, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Aromatase Inhibitors in Products Marketed as Dietary Supplements: Recall, FDA MedWatch
• ALLERGY ALERT: Oatmeal Raisin Cookies & Chocolate Chunk Cookies Sold at 7-eleven, FoodSafety.gov
• Hallmark Fisheries Issues Recall of Crab Meat Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Dough Masters Inc. Issues Recall of Oatmeal Raisin Cookies and Chocolate Chunk Cookies Due to Undeclared Walnuts, U.S. Food & Drug Administration (FDA)
• iForce Nutrition Issues a Voluntary Nationwide Recall of Reversitol a Product Marketed as a Dietary Supplement Containing ATD, U.S. Food & Drug Administration (FDA)
• FDA Office of Women's Health Fall 2010 eUpdate, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Actos (pioglitazone): Ongoing Safety Review - Potential Increased Risk of Bladder Cancer, FDA MedWatch
• FDA reviewing preliminary safety information on Actos (pioglitazone), 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, 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, U.S. Food & Drug Administration (FDA)
• FDA , U. of Md., train Bangladeshis on aquaculture safety, U.S. Food & Drug Administration (FDA)
• FDA hosts Middle East and North Africa food safety experts, U.S. Food & Drug Administration (FDA)
• FDA approves devices for heart failure patients, U.S. Food & Drug Administration (FDA)
• Twitter Chat at 3:30 pm ET Today: Food Safety for At-Risk People, FoodSafety.gov
• G.E.T. Issues Vouluntary Recall of ArimaDex, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - September Green Book Update, U.S. Food & Drug Administration (FDA)
• Kilosports Inc. Issues Voluntary Recall of Clomed, U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 15, 2010, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - BagEasy Manual Resuscitation Devices by Westmed, Inc.: Class 1 Recall, FDA MedWatch
• August 2010 Drug Safety Labeling Changes: 24 Medical Product Labels with changes to Warnings, Contraindications, Precautions, Adverse Reactions, FDA MedWatch
• Westmed, Inc. Issues Nationwide Recall of BagEasy Manual Resuscitation Devices, U.S. Food & Drug Administration (FDA)
• Forest Pharmaceuticals agrees to guilty plea for violating FDA laws, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Valcyte (valganciclovir hydrochloride) Label Change: Possible overdose in pediatric patients, FDA MedWatch
• FDA issues new dosing guide for children using Valcyte, U.S. Food & Drug Administration (FDA)
• The Affordable Care Act & Behavioral Health, HealthCare.gov
• FDA approves new drug for gout, U.S. Food & Drug Administration (FDA)
• Webinar on Generic Drugs, 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, 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, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recall: Libby & Kroger Corned Beef, Brushy Creek Beef Products, FoodSafety.gov
• Influenza Vaccination Information for Health Care Workers, U.S. Dept. of Health & Human Services
• How to Clean and Disinfect Schools to Help Slow the Spread of Flu, U.S. Dept. of Health & Human Services
• Get information about high-risk groups, flu symptoms and emergency warning signs, and get CDC recommendations., 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, FDA MedWatch
• FDA MedWatch - Gadolinium-based Contrast Agents: Class Labeling Change - Risk of Nephrogenic Systemic Fibrosis, FDA MedWatch
• FDA approves pediatric use of chemical poisoning treatment, U.S. Food & Drug Administration (FDA)
• The September 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
• FDA acts against 5 electronic cigarette distributors, U.S. Food & Drug Administration (FDA)
• FDA: New warnings required on use of gadolinium-based contrast agents, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recall: Milk, FoodSafety.gov
• Recall of Fluid Milk Products out of Midland Farms, Inc., U.S. Food & Drug Administration (FDA)
• Enforcement Report for September 8, 2010, U.S. Food & Drug Administration (FDA)
• How the Affordable Care Act Will Help Businesses and Unions Keep Early Retirees Covered, HealthCare.gov
• FDA MedWatch - AngioSculpt "EX" PTCA Scoring Balloon Catheter by AngioScore, Inc.: Recall - Risk of Catheter Separation, FDA MedWatch
• Undeclared Sulfites in "Rehmat" Brand Apricots, 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, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Warning: Discard cheeses from Estrella Family Creamery, FoodSafety.gov
• Cibo Vita issues Allergy Alert on Undeclared Sulfites in Mediterranean Mix of Woodpecker Brand, FoodSafety.gov
• FoodSafety.gov Recall: Hartz Naturals Real Beef Treats for Dogs, FoodSafety.gov
• FoodSafety.gov Recall: Egg Noodles & Wonton Skins, Possible Salmonella, FoodSafety.gov
• Sparboe Farms Provides Clarification on its Voluntary Recall of Fresh Shell Eggs, U.S. Food & Drug Administration (FDA)
• The Hartz Mountain Corporation Recalls Hartz Naturals Real Beef Treats Because of Possible Salmonella Health Risk, U.S. Food & Drug Administration (FDA)
• Real Taste Noodle Manufacture Recalls Egg Noodle Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA cautions consumers about Estrella Family Creamery cheeses, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Additional Materials for the AquAdvantage Salmon VMAC Meeting, U.S. Food & Drug Administration (FDA)
• Good Taste Noodle MFG Recalls "Egg Noodles and Wonton Skins" Because Of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recalls: Whole Foods Recalls Raw Goat Milk Cheese, FoodSafety.gov
• Whole Foods Market® Announces Recall of Morningland Dairy and Ozark Hills Farm Cheese, 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, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • HIV/AIDS Update - Tentiative approval of lamivudine, nevirapine, and stavudine fixed dose combination tablets, 150 mg/200 mg/30 mg, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recall: Cooked Shredded Pork Skin Products, FoodSafety.gov
• FoodSafety.gov Recall Expanded: Queso Fresco and Requeson (Ricotta), FoodSafety.gov
• Enforcement Report for September 1, 2010, U.S. Food & Drug Administration (FDA)
• What do consumers need to know about the recall of shell eggs?, U.S. Food & Drug Administration (FDA)
• Azteca Linda Corp. Expands Recall of Queso Fresco Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - P&G Voluntarily Recalls a Small Amount of Dry Cat Food, U.S. Food & Drug Administration (FDA)
• P&G Voluntarily Recalls a Small Amount of Dry Cat Food, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov News Update, FoodSafety.gov
  • <Possible follow-ups>
  • FoodSafety.gov News Update, FoodSafety.gov
• FoodSafety.gov Recall: Iams Cat Food Recalled from Stores in Loveland, Colorado, FoodSafety.gov
• QUESERIA CHIPILO INC. Recalls Cheese Products because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Tygacil (tigecycline): Label Change - Increased Mortality Risk, FDA MedWatch
• FoodSafety.gov Allergy Alert: Peanuts in "Mixed Nuts Fancy, No Peanuts", FoodSafety.gov
• FoodSafety.gov Recall: Morningland Dairy & Ozark Hills Farm cheeses, FoodSafety.gov
• The September 2010 MedSun Newsletter is now available..., U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - new guidances available, U.S. Food & Drug Administration (FDA)
• Torn & Glasser Issues Allergy Alert on Undeclared Peanuts Fancy, No Peanuts, U.S. Food & Drug Administration (FDA)
• FDA seeks court order against Michigan dairy, U.S. Food & Drug Administration (FDA)
• Paleta California Co. Announces Voluntary Recall of Frozen Mamey Paletas Because of Potential Contamination with Salmonella Typhi, 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, U.S. Food & Drug Administration (FDA)
• FDA launches new organizational performance management system, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Green Book August 2010 Update, 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, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recalls: "Fruiti Pops" Mamey Frozen Fruit Bars and Queseria Chipilo Cheese Products, FoodSafety.gov
• P&G Recalls Small Number of Bags of Cat Food From Stores in Loveland, Colorado, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recall: Ground Beef Distributed to BJ's Wholesale Club, FoodSafety.gov
• Sparboe Farms Initiated Voluntary Recall Fresh Shell Eggs, U.S. Food & Drug Administration (FDA)
• Fruiti Pops, Inc. Recalls "Fruiti Pops" Brand Mamey Frozen Fruit Bars Because of Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Queseria Chipilo Recalls Cheese Products Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Cal-Maine Foods, Inc. Clarifies Previous Statement on Nationwide Shell Egg Recall, U.S. Food & Drug Administration (FDA)
• Estimating Seasonal Influenza-Associated Deaths in the U.S: CDC Study Confirms Variability of Flu, U.S. Dept. of Health & Human Services
• FDA MedWatch - Huber Needles: Recall - Risk of Coring, FDA MedWatch
• FDA MedWatch - Fingerstick Devices to Obtain Blood Specimens: Initial Communication - Risk of Transmitting Bloodborne Pathogens, FDA MedWatch
• Enforcement Report for August 25, 2010, 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, U.S. Food & Drug Administration (FDA)
• Cardenas Market Brand Label Included in Wright County Egg Recall, U.S. Food & Drug Administration (FDA)
• FDA Warns Consumers to Avoid TimeOut Capsules, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recalls: Queso Fresco and Queso Hebra, FoodSafety.gov
• Azteca Linda Corp. Recalls Queso Fresco and Queso Hebra because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Veterinary Medicine Advisory Committee Meeting Announcement, 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, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Alert: Updated List of Recalled Egg Brands, FoodSafety.gov
• The Power of Information at Your Fingertips, HealthCare.gov
• FDA MedWatch - Mr. Magic Male Enhancer: Undeclared Drug Ingredient, FDA MedWatch
• FDA releases guidance on federal menu labeling requirements, U.S. Food & Drug Administration (FDA)
• FDA Warns of Possible Dangers from Portable Foot-Tanning Device, U.S. Food & Drug Administration (FDA)
• Integra Issues URGENT Worldwide Recall of NeuroBalloonTM Catheter, 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, 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, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recalls: 380,000 lbs of Deli Meat Products, Possible Listeria, FoodSafety.gov
• FDA MedWatch - INOMAX DS Drug-Delivery System: Class I Recall - Risk of Interruption of Drug Flow, FDA MedWatch
• NY Fish Inc Issues an alert on uneviscerated fish, U.S. Food & Drug Administration (FDA)
• Study: Presence of murine leukemia virus found in CFS Patients, others, U.S. Food & Drug Administration (FDA)
• NIH Office of Research on Women's Health - 20th Anniversary Celebration, U.S. Food & Drug Administration (FDA)
• Luberski Inc. Initiates Voluntary Recall of Large Fresh Shell Eggs Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update - Tentative approval of generic atazanavir sulfate capsules, 300 mg, 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, U.S. Food & Drug Administration (FDA)
• GloryBee Foods Recalls Whole Raw Pistachio and Whole Raw Pistachio Kernels Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Austinuts Wholesale, Inc. Announces Voluntary Recall of Pistachio Kernel Products, U.S. Food & Drug Administration (FDA)
• Review Calls for New Federal Approach to Medical Countermeasures, U.S. Dept. of Health & Human Services
• Salmonella in Alfalfa Sprouts, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Alert: URGENT Nationwide Frozen Mamey Fruit Pulp Recall, FoodSafety.gov
• Hillandale Farms of Iowa Conducts Nationwide Voluntary Recall of Shell Eggs Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• Urgent Nationwide Frozen Mamey Fruit Products Recall, U.S. Food & Drug Administration (FDA)
• Stalevo(carbidopa/levodopa and entacapone): Ongoing Safety Review: Possible increased cardiovascular risk, FDA MedWatch
• FoodSafety.gov Alert: URGENT Nationwide Egg Recall, FoodSafety.gov
• FoodSafety.gov Recalls: "La Nuestra" Frozen Mamey Pulp, FoodSafety.gov
• Montalvan's Sales, Inc. Recalls "La Nuestra" Brand Frozen Mamey Because of Potential Health Risk, U.S. Food & Drug Administration (FDA)
• Urgent Nationwide Egg Recall, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Updated Minor Use/Minor Species Designations List, 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, U.S. Food & Drug Administration (FDA)
• U.S. Marshals seize food from rodent-infested Ga. warehouse, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 18, 2010, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recall: Nationwide Egg Recall Expanded, FoodSafety.gov
• Wright County Egg Expands Nationwide Voluntary Recall of Shell Eggs Because of Possible Health Risk, U.S. Food & Drug Administration (FDA)
• NuCal Foods Conducts Recall of Shell Eggs Supplied from Wright County Egg Because of Possible Health Risk, 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, 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, U.S. Food & Drug Administration (FDA)
• Glow Industries, Inc. Issues Nationwide Recall of Mr. Magic Male Enhancer from Don Wands Amended, U.S. Food & Drug Administration (FDA)
• Undeclared Sulfites in "Golden Bridge" Dried Dates, 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, 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, U.S. Food & Drug Administration (FDA)
• How the Affordable Care Act Will Hold Insurers Accountable, HealthCare.gov
• Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, U.S. Food & Drug Administration (FDA)
  • Update of CVM's What's New - Updated Cumulative Veterinary Adverse Drug Experience (ADE) Reports, 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, U.S. Food & Drug Administration (FDA)
• How is a potential advisory committee member screened for conflicts of interests?, U.S. Food & Drug Administration (FDA)
• What are the qualifications of a scientific member of an advisory committee?, U.S. Food & Drug Administration (FDA)
• What is a financial conflict of interest waiver?, U.S. Food & Drug Administration (FDA)
• What is a conflict of interest?, U.S. Food & Drug Administration (FDA)
• What is an FDA Advisory Committee?, U.S. Food & Drug Administration (FDA)
• How does an individual become a member of an FDA advisory committee?, U.S. Food & Drug Administration (FDA)
• Nationwide Milk Allergen Recall of Kroger "Meals Made Simple Shrimp Linguini", 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, U.S. Food & Drug Administration (FDA)
• Staphylococcus Aureus in Queso Cotija Cheese, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Recalls: Frozen Mamey Fruit Pulp and Queso Cotija Cheese, FoodSafety.gov
• FDA MedWatch - Midodrine hydrochloride: FDA Proposes Withdrawal of Low Blood Pressure Drug, FDA MedWatch
• Update of CVM's What's New - New Issue of FDA Veterinarian Newsletter, 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, U.S. Food & Drug Administration (FDA)
• FDA Proposes Withdrawal of Low Blood Pressure Drug, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Guidance - Residual Solvents in New Veterinary Medicinal Products, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov: Nationwide Egg Recall, Illnesses Reported, FoodSafety.gov
• Wright County Egg Conducts Nationwide Voluntary Recalls of Shell Eggs Because of Possible Health Risk, 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, U.S. Food & Drug Administration (FDA)
• FDA approves ella[TM] tablets for prescription emergency contraception, 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, FDA MedWatch
• What is an FDA Drug Safety Communication?, U.S. Food & Drug Administration (FDA)
• How does the FDA use Advisory Committees to make decisions about drugs?, U.S. Food & Drug Administration (FDA)
• Strong America Ltd. Issues an Alert on Undeclared Sulfites in Golden Smell Brand "Dried Potato", U.S. Food & Drug Administration (FDA)
  • <Possible follow-ups>
  • Strong America Ltd. Issues an Alert on Undeclared Sulfites in Golden Smell Brand "Dried Potato", U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Prolatis': Recall - Undeclared Drug Ingredient Sulfoaildenafil, FDA MedWatch
• FDA MedWatch - Lamictal (lamotrigine): Label Change - Risk of Aseptic Meningitis, FDA MedWatch
• Prolatis' Issues a Voluntary Nationwide Recall of its product Prolatis' Marketed as Dietary Supplement prior to August 9, 2010, U.S. Food & Drug Administration (FDA)
• Goya Foods, Inc. Announces Voluntary Recall of Frozen Mamey Pulp, U.S. Food & Drug Administration (FDA)
• Building a healthier America, one community at a time, HealthCare.gov
• FDA: Aseptic Meningitis Risk with Use of Seizure Drug Lamictal, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 11, 2010, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - Novacare LLC Products: Recall - Undeclared Drug Ingredient, FDA MedWatch
• WHO Recommendations for the Post-pandemic Period, U.S. Dept. of Health & Human Services
• WHO Director-General Statement, U.S. Dept. of Health & Human Services
• FoodSafety.gov Recall: Fresh Express Veggie Lovers Salad, FoodSafety.gov
• 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, U.S. Food & Drug Administration (FDA)
• Ikaria® Recalls INOMAX® DS Drug-Delivery System, U.S. Food & Drug Administration (FDA)
• Novacare LLC Conducts Voluntary Nationwide Recall of Products Found to Contain Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov News & Features Update, FoodSafety.gov
  • <Possible follow-ups>
  • FoodSafety.gov News & Features Update, FoodSafety.gov
  • FoodSafety.gov News & Features Update, FoodSafety.gov
• FDA: Salmonella risk from frozen rodents fed to reptiles, U.S. Food & Drug Administration (FDA)
• Questions and Answers: CSL Seasonal Influenza Vaccine Safety in the U.S., U.S. Dept. of Health & Human Services
• Recommended Flu Vaccines for Different Age Groups, 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, U.S. Food & Drug Administration (FDA)
• FDA MedWatch - August 2010 FDA Patient Safety News now available, FDA MedWatch
• FDA MedWatch - Inferior Vena Cava (IVC) Filters: Initial Communication: Risk of Adverse Events with Long Term Use, FDA MedWatch
• FoodSafety.gov Recalls: Allergy Alert (Chocolate Covered Nuts) and Truffle Puree, FoodSafety.gov
• FDA MedWatch - Solo Slim, Solo Slim Extra Strength: Recall - Undeclared Drug Ingredient, FDA MedWatch
• FDA MedWatch - Revivexxx Extra Strength: Recall - Undeclared Drug Ingredient, FDA MedWatch
• The August 2010 FDA Patient Safety News is now available..., U.S. Food & Drug Administration (FDA)
• EZVille, Ltd. Issues a Voluntary Nationwide Recall of Revivexxx® Extra Strength Found to Contain an Undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• EZVille, Ltd. Issues a Voluntary Nationwide Recall of Solo Slim® Found to Contain an undeclared Drug Ingredient, U.S. Food & Drug Administration (FDA)
• South Bend Chocolate Company Announces Nationwide Recall of Bountiful Blend Chocolates Due to Undeclared Tree Nuts, U.S. Food & Drug Administration (FDA)
• FDA Seeks Injunction Against Colorado Manufacturer of Cultured Cell Product, U.S. Food & Drug Administration (FDA)
• HIV/AIDS Update -Tentative approval of lamivudine and stavudine Fixed Dose Combination tablets, U.S. Food & Drug Administration (FDA)
• FoodSafety Recall: Frozen Ground Beef, FoodSafety.gov
• Product Recall - Eugenio Brezzi Truffle Puree, U.S. Food & Drug Administration (FDA)
• Update of CVM's What's New - Guidance for Industry Drug Substance Chemistry, Manufacturing, and Controls Information, U.S. Food & Drug Administration (FDA)
• Enforcement Report for August 4, 2010, 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, 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, U.S. Food & Drug Administration (FDA)
• Who makes sure the food I buy at the grocery store is safe to eat?, U.S. Food & Drug Administration (FDA)
• Upcoming Webinar Tuesday, August 10th - Using a Food Label to Make Smart Food Choices, U.S. Food & Drug Administration (FDA)
• FDA Issues Assessments of the 510(k) Program and Use of Science in Decision-Making, U.S. Food & Drug Administration (FDA)
• FoodSafety.gov Allergy Alert: Canned Meatballs in Sauce Contain Eggs, FoodSafety.gov
• Update of CVM's What's New - P&G Expands Voluntary Limited Recall of Specialized Dry Pet Foods Due to Possible Health Risk, U.S. Food & Drug Administration (FDA)