Wright Profemur Hip Replacement Docum...

Wright Profemur Hip Replacement Documents Subpoenaed By U.S. Attorney's Office

There are 3 comments on the The Beaumont Enterprise story from Aug 16, 2012, titled Wright Profemur Hip Replacement Documents Subpoenaed By U.S. Attorney's Office. In it, The Beaumont Enterprise reports that:

Wright Profemur Hip Replacement Documents Subpoenaed By U.S. Attorney's Office Wright Profemur hip replacement implants subject of subpoena sent to hip manufacturer, Wright Medical Technology, Inc., Bernstein Liebhard LLP reports.Wright Profemur hip replacement devices are the subject of a federal subpoena served upon Wright Medical Technology ... (more)

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Kat

Atlanta, GA

#1 Aug 31, 2012
People may need to be aware that in addition to the hip replacement devices failing and requiring revision surgery, there is also a risk for metal poisoning in the blood and surrounding tissues from all-metal implants. The metal parts grind against each other, causing toxic metal shavings to become dispersed in the body. The metal poisoning, metallosis, might increase the risk of kidney and bladder cancers. If you or a loved one have experienced any of the complications associated with metal hip replacement parts, you may find helpful information at http://www.depuypinnaclelawsuit.com .
Rhonda

Atlanta, GA

#2 Sep 14, 2012
Hip replacement surgery has been a consistent subject of medical news because of the infamous DePuy hip replacement recall. According to DePuy, It is important for all patients to have their hip evaluated by their doctor, though most patients will not need additional surgery as a result of this recall.
For more information about hip problems, refer to http://www.depuyhipreplacementlawsuit.com
Melena K

Phoenix, AZ

#3 Mar 1, 2013
There are several cases wherein patients experience so much pain after a hip replacement surgery. Other instances require a revision or second surgery. One reason is a defective hip device. In 2010, Johnson&Johnson issued a worldwide recall of two hip replacement devices (manufactured by its subsidiary DePuy Orthopaedics) because of hip replacement problems. These devices are the ASR XL Acetabular System and the ASR Hip Resurfacing System. The company cited early failure of the devices, resulting in approximately one out of eight patients’ requiring a “revision surgery." This surgery is often more difficult and painful than the original hip replacement procedure. The website depuysettlements. com provides a wide-ranging information on this.

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