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As of 2018, J&J committed to working with the Indian government to support all Indian ASR patients. In late 2018, an Indian government report, the accuracy of which has been disputed by J&J, proposed that each patient who had a faulty implant should receive a lump sum payment of ₹2 million ( US$27,812 ).
At 120,000 square feet (11,000 m 2), this facility occupies a fraction of the J&J campus, which encompasses 69 acres (280,000 m 2) in total. Manufacturing at JJM began in February 2008. On August 24, 2010, DePuy recalled [4] all ASR hip implant systems sold since 2003.
In recent decades, the most successful and common form of arthroplasty is the surgical replacement of a joint or joint surface with a prosthesis. For example, a hip joint that is affected by osteoarthritis may be replaced entirely (total hip arthroplasty) with a prosthetic hip.
J&J's Ethicon unit confirmed serious injuries to two patients, related to the use of the recalled product, the FDA said https://bit.ly/2Ef29CR. U.S. FDA labels J&J surgical staplers' recall as ...
The 2010 Johnson & Johnson children's product recall involved 43 over-the-counter children's medicines announced by McNeil Consumer Healthcare, a subsidiary of Johnson & Johnson, on April 30, 2010. Medications in the recall included liquid versions of Tylenol, Tylenol Plus, Motrin, Zyrtec, and Benadryl. The products were recalled after it was ...
The U.S. health regulator said it had received reports of pediatric and adult patients suffering burn injuries when the tools, sold under the brand names MEGA 2000 and MEGA SOFT Reusable Patient ...
The affected batches were sold in South Africa, Eswatini, Rwanda, Kenya, Tanzania and Nigeria, the statement added. The recall follows a report by the regulator's Nigerian counterpart on Wednesday ...