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      J&J Settles Talc Mesothelioma Settlement

      By Sandra Dalton, Staff Writer On January 6, 2020, Superior Court Judge Stephen Kaus announced that Johnson & Johnsons (J&J) had agreed to … [Read More...]

      Advantage Health Matters Inc Recalls “Organic Jumbo Pumpkin Seeds” Because of Possible Health Risk

      Summary Company Announcement Date: May 08, 2025 FDA Publish Date: May … [Read More...]

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You are here: Home / Archives for Food Recalls / FDA Press Releases

Personal Care Products Conducts Nationwide Recall of Non-Acetone Nail Polish Remover

April 30, 2009 By The FDA Leave a Comment

CONTACT: LAWRENCE WEISBERG 248-258-1555 FOR IMMEDIATE RELEASE -- APRIL 29, 2009 -- PERSONAL CARE PRODUCTS OF BINGHAM FARMS, MI IS VOLUNTARILY CONDUCTING A NATIONWIDE RECALL OF ALL LOTS OF PERSONAL CARE NON-ACETONE NAIL POLISH REMOVER, CONDITIONER ENRICHED WITH GELATIN, 6 FL. OZ., UPC 4815592076, BECAUSE IT DOES NOT MEET PRODUCT SPECIFICATIONS AND … [Read more...]

Filed Under: FDA Press Releases

Recall Of Prescription Cough and Cold Drugs by Neilgen Pharma and Advent Pharmaceutical

April 22, 2009 By The FDA 1 Comment

CONTACT: BHARAT PATEL, PRESIDENT (609) 448-5500 NEILGEN PHARMA INC. OF WESTMINSTER, MD AND ADVENT PHARMACEUTICAL OF EAST WINDSOR, NJ ARE RECALLING ALL PRESCRIPTION COUGH AND COLD DRUG PRODUCTS SOLD ON OR AFTER MARCH 5, 2008. NEILGEN PHARMA AND ADVENT PHARMACEUTICAL ARE CONTRACT MANUFACTURERS FOR THESE PRODUCTS AND ARE RECALLING THE LISTED PRODUCTS … [Read more...]

Filed Under: FDA Press Releases

ION Labs Inc. Recalls Influend Cough and Cold Products, in Alabama

April 17, 2009 By The FDA Leave a Comment

ION LABS INC. OF CLEARWATER, FL. IS VOLUNTARILY RECALLING ALL OF THE INFLUEND COUGH AND COLD PRODUCTS SOLD ON OR AFTER MAY 30, 2008. ION LABS INC. IS RECALLING THE LISTED PRODUCTS DUE TO THE PRODUCTS NOT TESTED IN CONFORMANCE WITH THE SPECIFICATIONS OF THE LAB, THEREFORE THE PRODUCTS MAY HAVE A POSSIBILITY TO BE SUPER POTENT. POSSIBLE COMPLICATIONS … [Read more...]

Filed Under: FDA Press Releases

Class I Recall of Intra Aortic Balloon Pump (IAB) Catheters by Arrow International

April 15, 2009 By The FDA Leave a Comment

CONTACT: INVESTORS:  JAKE ELGUICZE   610-948-2836 MEDIA:    JULIE MCDOWELL    610-948-2829 TELEFLEX MEDICAL ANNOUNCED TODAY THAT THE U.S. FOOD AND DRUG ADMINISTRATION (FDA) HAS CLASSIFIED THE VOLUNTARY MEDICAL DEVICE RECALL INITIATED ON FEBRUARY 2, 2009 BY ARROW INTERNATIONAL’S CARDIAC CARE … [Read more...]

Filed Under: FDA Press Releases

FDA Statement on the Voluntary Withdrawal of Raptiva From the U.S. Market

April 9, 2009 By The FDA 1 Comment

GENENTECH, THE MANUFACTURER OF THE PSORIASIS DRUG RAPTIVA (EFALIZUMAB), ANNOUNCED THAT IT HAS BEGUN A VOLUNTARY, PHASED WITHDRAWAL OF RAPTIVA FROM THE U.S. MARKET. THE COMPANY IS TAKING THIS ACTION BECAUSE OF A POTENTIAL RISK TO PATIENTS OF DEVELOPING PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY (PML), A RARE, SERIOUS, PROGRESSIVE NEUROLOGIC DISEASE … [Read more...]

Filed Under: FDA Press Releases

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J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Advantage Health Matters Inc Recalls “Organic Jumbo Pumpkin Seeds” Because of Possible Health Risk

May 8, 2025 By The FDA

Yamaha Corporation of America Recalls Power Adaptors for Digital Pianos and Music Workstations Due to Burn and Fire Hazards

May 7, 2025 By The CPSC

DEMDACO Recalls Maril Brand Scented Candles Due to Laceration and Fire Hazards

May 7, 2025 By The CPSC

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Xylolin Peg Doll Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violation of Federal Regulations for Toys; Sold Exclusively on Amazon.com by Babywants

May 7, 2025 By The CPSC

Igloo Expands Recall of 90 Qt. Rolling Coolers Due to Fingertip Amputation and Crushing Hazards; Total Recalled Now Nearly 1.2 Million

May 7, 2025 By The CPSC

Deuter Recalls Kid Comfort, Kid Comfort Pro and Kid Comfort Active Child Carriers Due to Fall Hazard

May 7, 2025 By The CPSC

Delta Gas Ball Valves Recalled Due to Fire and Burn Hazards; Manufactured by Masco Canada

May 7, 2025 By The CPSC

FDA Advises Consumers, Tattoo Artists, and Retailers to Avoid Using or Selling Certain Sacred Tattoo Ink Products Contaminated with Microorganisms

May 6, 2025 By The FDA

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Delta Gas Ball Valves Recalled Due to Fire and Burn Hazards; Manufactured by Masco Canada

May 7, 2025 By The CPSC

FDA Advises Consumers, Tattoo Artists, and Retailers to Avoid Using or Selling Certain Sacred Tattoo Ink Products Contaminated with Microorganisms

May 6, 2025 By The FDA

New England Village Foods Issues Allergy Alert on Undeclared Almonds and Sesame in “19th Hole Snack Mix”

May 6, 2025 By The FDA

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Recent Posts

  • Advantage Health Matters Inc Recalls “Organic Jumbo Pumpkin Seeds” Because of Possible Health Risk
  • Yamaha Corporation of America Recalls Power Adaptors for Digital Pianos and Music Workstations Due to Burn and Fire Hazards
  • DEMDACO Recalls Maril Brand Scented Candles Due to Laceration and Fire Hazards
  • Legend Brands Recalls Bliss Hair Dryers Due to Risk of Serious Injury or Death from Electrocution and Shock Hazards; Sold Exclusively at Burlington Stores
  • Sanven Technology Recalls Vevor Cable Railing Kits Due to Entrapment Hazard
  • Xylolin Peg Doll Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violation of Federal Regulations for Toys; Sold Exclusively on Amazon.com by Babywants
  • Igloo Expands Recall of 90 Qt. Rolling Coolers Due to Fingertip Amputation and Crushing Hazards; Total Recalled Now Nearly 1.2 Million
  • Deuter Recalls Kid Comfort, Kid Comfort Pro and Kid Comfort Active Child Carriers Due to Fall Hazard
  • Delta Gas Ball Valves Recalled Due to Fire and Burn Hazards; Manufactured by Masco Canada
-- See More Recall News

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