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The 2010 DePuy Hip Replacement Recall was instituted when DePuy Orthopaedics, Inc., a division of Johnson and Johnson, recalled its ASR XL Acetabular metal-on-metal hip replacement system on August 24, 2010. [1] [2]
On August 24, 2010, DePuy, a subsidiary of American giant Johnson & Johnson, recalled its ASR (articular surface replacement) hip prostheses from the market. DePuy said the recall was due to unpublished National Joint Registry data showing a 12% revision rate for resurfacing at five years and an ASR XL revision rate of 13%.
The manufacturers or distributors of the product carry out most recalls of products regulated by FDA voluntarily. In some instances, a company discovers that one of its products is defective and recalls it entirely on its own. In others, FDA informs a company of findings that one of its products is defective and suggests or requests a recall.
November 15, 2023 at 10:33 AM. When Judith Gregory’s left eye became red, teary and painful last year, she made the first of many trips to her eye doctor to deal with complications. “At that ...
The recall affects 569,000 parts — this includes 105,000 that were previously recalled in August 2018 (at the time, the company advised customers to pause use and offered repair kits as a remedy).
Vitamix recalls almost 570,000 blender parts. Ramishah Maruf, CNN. June 20, 2024 at 6:34 PM. US Consumer Product Safety Commission. Parts of a pricey blender that can cost up to $990 can cause ...
Drug recall. A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug ...
January 10, 2023 at 11:59 AM. Tracy Glantz/tglantz@thestate.com. Veterans are being advised to stop using drugs produced by Lexington County-based Nephron Pharmaceuticals, according to the U.S ...