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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

Cardiovascular Systems Recalls ViperSheath Sheath Introducer

November 18, 2009 By The FDA Leave a Comment

Cardiovascular Systems, Inc. has announced a voluntary recall of all lots of the ViperSheathTMSheath Introducer on behalf of Thomas Medical due to reports about stretching or fracture of the sheath during use. CSI initiated the nationwide recall on November 2, 2009. The ViperSheathTM Sheath Introducer is a product developed and manufactured by … [Read more...]

Filed Under: FDA Press Releases

Cardiac Science Notifies AED Customers of Nationwide Voluntary Medical Device Correction

November 15, 2009 By The FDA Leave a Comment

Cardiac Science Corporation is initiating a voluntary field correction after it was determined certain automated external defibrillators (AEDs) may experience a rare product issue in which the AED may not be able to deliver therapy during a resuscitation attempt. Device failure may affect resuscitation of the patient, which could lead to serious … [Read more...]

Filed Under: FDA Press Releases

IDS Sports Conducts a Voluntary Nationwide Recall of Bromodrol, Dual Action Grow Tabs, Grow Tabs, Mass Tabs, and Ripped Tabs TR

November 14, 2009 By The FDA 1 Comment

IDS Sports announced today that it is conducting a voluntary nationwide recall of five of the company’s dietary supplement products sold under the following names: Bromodrol, Dual Action Grow Tabs, Grow Tabs, Mass Tabs, and Ripped Tabs TR. The Food And Drug Administration (FDA) has notified IDS Sports that the recalled products contain the … [Read more...]

Filed Under: FDA Press Releases

GMP Herbal Products Recalls Weight Loss Supplement Found to Contain Undeclared Drug Ingredients

November 14, 2009 By The FDA Leave a Comment

GMP Herbal Products, Inc. has been informed by the Food and Drug Administration (FDA) that Pai You Guo, a weight loss dietary supplement, sold and marketed by the firm contains undeclared drug ingredients. FDA lab analyses of dietary supplements distributed by the company were found to contain undeclared sibutramine, an FDA-approved drug used as … [Read more...]

Filed Under: FDA Press Releases

Hospira Recalls Certain Lots of Liposyna and Propofol Products: May Contain Particulate Matter

November 10, 2009 By The FDA Leave a Comment

Hospira, Inc. (NYSE: HSP), a global specialty pharmaceutical and medication delivery company, is voluntarily recalling 85 lots of Liposynâ?¢ II 10%, Liposyn II 20%, Liposyn III 10%, Liposyn III 20%, Liposyn III 30% and 73 lots of Propofol Injectable Emulsion 1% products that begin with the lot numbers 79 and 80 because some of the containers may … [Read more...]

Filed Under: FDA Press Releases

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Economic Consulting

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

New Grains Gluten Free Bakery Issues Allergy Alert on Undeclared Eggs, Soy, and Milk in Bakery Products

May 7, 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

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Sanven Technology Recalls Vevor Cable Railing Kits Due to Entrapment Hazard

May 7, 2025 By The CPSC

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

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

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

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Recent Posts

  • Advantage Health Matters Inc Recalls “Organic Jumbo Pumpkin Seeds” Because of Possible Health Risk
  • New Grains Gluten Free Bakery Issues Allergy Alert on Undeclared Eggs, Soy, and Milk in Bakery Products
  • 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
-- See More Recall News

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