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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...]

      South Asian Food Inc. Issues Allergy Alert on Undeclared Peanuts in “Bengal King Family Pack Vegetable Singara”

      Summary Company Announcement Date: May 16, 2025 FDA Publish Date: May … [Read More...]

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

Verathon Inc. Issues Voluntary Recall of Certain GlideScope GVL Video Laryngoscope Reusable Blades

December 1, 2012 By The FDA Leave a Comment

Verathon Inc., Bothell, Washington, is initiating a voluntary recall of GlideScope GVL Video Laryngoscopes reusable blades that were manufactured between December 2010 and August 2011. These laryngoscope blades have been found to be prone to developing cracks and/or breaking across the tip of the blade, which potentially could result in pieces of … [Read more...]

Filed Under: FDA Press Releases

Zi Xiu Tang Success, LLC Issues Voluntary Nationwide Recall Of Classic Zi Xiu Tang Bee Pollen Capsules And Ultimate Formula Capsules Due To Undeclared Sibutramine

November 2, 2012 By The FDA Leave a Comment

Trexlertown, PA, Zi Xiu Tang Success, LLC is voluntarily recalling four lots of Classic Zi Xiu Tang Bee Pollen Capsules, and three lots of Ultimate Formula Capsules to the consumer level. These products have been found to contain undeclared Sibutramine. Sibutramine was a previously approved controlled substance that was removed from the U.S. market … [Read more...]

Filed Under: FDA Press Releases

Hospira Issues A Voluntary Nationwide Recall Of Symbiq Infusion Systems Due To Inaccurate ResponseOf The Touch Screen To User Selection/Input

November 2, 2012 By The FDA Leave a Comment

Hospira, Inc. (NYSE: HSP), announced today it is initiating a voluntary nationwide Class I recall of Symbiq™ infusion systems (list number 16026 Symbiq™ One-Channel Infuser and list number 16027 Symbiq™ Two-Channel Infuser, all serial numbers). This action is due to infusion pump LCD touch screens that may not respond to user selection, resulting … [Read more...]

Filed Under: FDA Press Releases

Ameridose Issues Recall of All Products

November 2, 2012 By The FDA Leave a Comment

Ameridose today announced it will commence a voluntary recall of any unexpired products remaining in circulation. This action is voluntary, and represents an expansion of our cooperation with the U.S.Food and Drug Administration and the Massachusetts Board of Registration in Pharmacy. During the course of its on-going inspection of our facility, … [Read more...]

Filed Under: FDA Press Releases

HeartSine Technologies, Ltd. Issues Global Correction Of Samaritan® 300/300P PAD

October 26, 2012 By The FDA Leave a Comment

On September 13, 2012, HeartSine Technologies, Ltd. initiated a voluntary global correction of certain Samaritan® 300/300P PAD public access defibrillators to address two separate issues that may affect the ability to deliver therapy to a patient in a sudden cardiac arrest (SCA) event, if needed. Certain Samaritan® 300/300P PAD devices manufactured … [Read more...]

Filed Under: FDA Press Releases

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J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

South Asian Food Inc. Issues Allergy Alert on Undeclared Peanuts in “Bengal King Family Pack Vegetable Singara”

May 16, 2025 By The FDA

LivingCaring Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violation of Federal Regulations for Adult Portable Bed Rails; Imported by Shanghai Kai Rong Xin Xi Ke Ji

May 14, 2025 By The CPSC

NICREW Submersible RGB LED Lights Recalled Due to Risk of Serious Injury or Death from Ingestion Hazard; Violations of Federal Regulations for Consumer Products with Coin Batteries; Sold on Amazon by Nicrew

May 14, 2025 By The CPSC

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Child Safety Gates Recalled Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violations of Federal Regulation for Gates and Enclosures; Imported by Yiwu Baili Import and Export; Sold on Amazon.com

May 14, 2025 By The CPSC

Leon Rading Recalls Digital Wall Clocks Due to Risk of Serious Injury or Death from Ingestion Hazard; Violations of Federal Regulations for Consumer Products with Coin Batteries; Sold Exclusively on Amazon.com

May 14, 2025 By The CPSC

KTM Recalls Off-Road Motorcycles Due to Crash Hazard Recall

May 14, 2025 By The CPSC

Fat Brain Recalls Rollers Tile Toys Used in PlayTab Modular Activity Boards Due to Magnet Ingestion Hazard; Risk of Serious Injury or Death; Violation of Federal Regulations for Toy Magnets

May 14, 2025 By The CPSC

FidgetThings Recalls Chill Pill Magnetic Haptic Fidget Toys Red Bumpy Due to Risk of Serious Injury or Death from Ingestion; Violation of Federal Regulations for Magnets; Sold Exclusively on FidgetThings.com

May 14, 2025 By The CPSC

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Fat Brain Recalls Rollers Tile Toys Used in PlayTab Modular Activity Boards Due to Magnet Ingestion Hazard; Risk of Serious Injury or Death; Violation of Federal Regulations for Toy Magnets

May 14, 2025 By The CPSC

FidgetThings Recalls Chill Pill Magnetic Haptic Fidget Toys Red Bumpy Due to Risk of Serious Injury or Death from Ingestion; Violation of Federal Regulations for Magnets; Sold Exclusively on FidgetThings.com

May 14, 2025 By The CPSC

Polaris Industries Recalls Ranger XP 1000 NorthStar and Ranger XP 1000 NorthStar Crew Recreational Off-Road Vehicles Due to Injury Hazard

May 14, 2025 By The CPSC

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Recent Posts

  • South Asian Food Inc. Issues Allergy Alert on Undeclared Peanuts in “Bengal King Family Pack Vegetable Singara”
  • LivingCaring Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violation of Federal Regulations for Adult Portable Bed Rails; Imported by Shanghai Kai Rong Xin Xi Ke Ji
  • NICREW Submersible RGB LED Lights Recalled Due to Risk of Serious Injury or Death from Ingestion Hazard; Violations of Federal Regulations for Consumer Products with Coin Batteries; Sold on Amazon by Nicrew
  • Boyro Baby Recalls High Chairs Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violations of Federal Regulations for High Chairs; Sold Exclusively on Amazon.com
  • BuddyLove Recalls Children’s Mini Danica Loungewear Sets Due to Risk of Serious Injuries or Death from Burn Hazard; Violation of Federal Regulations for Children’s Sleepwear
  • Child Safety Gates Recalled Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violations of Federal Regulation for Gates and Enclosures; Imported by Yiwu Baili Import and Export; Sold on Amazon.com
  • Leon Rading Recalls Digital Wall Clocks Due to Risk of Serious Injury or Death from Ingestion Hazard; Violations of Federal Regulations for Consumer Products with Coin Batteries; Sold Exclusively on Amazon.com
  • KTM Recalls Off-Road Motorcycles Due to Crash Hazard Recall
  • Fat Brain Recalls Rollers Tile Toys Used in PlayTab Modular Activity Boards Due to Magnet Ingestion Hazard; Risk of Serious Injury or Death; Violation of Federal Regulations for Toy Magnets
-- See More Recall News

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