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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...]

      CHS Inc. Recalls Payback Champion Lamb Feed Due to Elevated Copper Health Risk

      Summary Company Announcement Date: July 09, 2025 FDA Publish Date: July … [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

CHS Inc. Recalls Payback Champion Lamb Feed Due to Elevated Copper Health Risk

July 9, 2025 By The FDA

Mondelēz Global LLC Conducts U.S. Voluntary Recall of Four Carton Sizes of RITZ Peanut Butter Cracker Sandwiches Due to Labeling Error

July 8, 2025 By The FDA

Natureen International Inc. Recalls Wei-Chuan Dried Black Fungus Slice (2.5oz) Because of Possible Health Risk

July 8, 2025 By The FDA

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Harbor Freight Tools Recalls Predator 2000-Watt Power Stations Due to Shock Hazard

July 2, 2025 By The CPSC

DEWALT Recalls Grinder Flap Discs Due to Laceration and Injury Hazards

July 2, 2025 By The CPSC

Trane Recalls Gas/Electric Packaged Units Due to Risk of Gas Leak, Fire Hazard

July 2, 2025 By The CPSC

Jeriflyer Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment Hazard; Violation of the Virginia Graeme Baker Pool and Spa Safety Act; Sold on Amazon by Junjuanshop

July 2, 2025 By The CPSC

Positec Recalls Electric Corded Chainsaws and Pole Saws Due to Laceration Hazard

July 2, 2025 By The CPSC

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Jeriflyer Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment Hazard; Violation of the Virginia Graeme Baker Pool and Spa Safety Act; Sold on Amazon by Junjuanshop

July 2, 2025 By The CPSC

Positec Recalls Electric Corded Chainsaws and Pole Saws Due to Laceration Hazard

July 2, 2025 By The CPSC

Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Cefazolin for Injection Due to Product Mispackaging

June 27, 2025 By The FDA

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  • CHS Inc. Recalls Payback Champion Lamb Feed Due to Elevated Copper Health Risk
  • Mondelēz Global LLC Conducts U.S. Voluntary Recall of Four Carton Sizes of RITZ Peanut Butter Cracker Sandwiches Due to Labeling Error
  • Natureen International Inc. Recalls Wei-Chuan Dried Black Fungus Slice (2.5oz) Because of Possible Health Risk
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  • Harbor Freight Tools Recalls Predator 2000-Watt Power Stations Due to Shock Hazard
  • DEWALT Recalls Grinder Flap Discs Due to Laceration and Injury Hazards
  • Trane Recalls Gas/Electric Packaged Units Due to Risk of Gas Leak, Fire Hazard
  • Jeriflyer Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment Hazard; Violation of the Virginia Graeme Baker Pool and Spa Safety Act; Sold on Amazon by Junjuanshop
-- See More Recall News

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