Patients With Defective DePuy ASR Hip Implants Should Consider The ARP Wave

In the wake of DePuy Orthopedics, Inc.’s recall of defective ASR hip implant devices, patients and their physicians have been searching for ways to mediate the potential health risks involved. With complications ranging from dislocation of the implant components and bone fractures at the hip, to metal poisoning, or metallosis, finding an accessible, effective treatment is imperative.
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Recall of Artificial Hip Causes Johnson & Johnson 2012 Earnings Forecast to Dip

The pharmaceutical giant, Johnson & Johnson, has been given a 2012 earnings forecast which is below the previous estimates present by financial analysts due to the number of DePuy hip replacements which were recalled. In fact, recent reports state Johnson & Johnson takes $3 billion charge for hip recall.
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Taking Charge: A Blueprint for DePuy Hip Implant Recipients to Follow for Successful Recovery

While the FDA began receiving complaints regarding the failure of hip replacement devices manufactured by DePuy Orthopedics (a subsidiary of Johnson & Johnson) for some time, there was not a DePuy hip extensive recall on the device until August of 2010.
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“Hip” Definitions: A Discussion of Medical Terms Every DePuy Hip Implant Recipient Should Know

July of 2003 saw the worldwide introduction of the metal-on-metal hip replacement by DePuy, although these devices were not used for hip replacement surgeries in the United States until 2005.
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Johnson & Johnson Takes $3 Billion Dollar Fourth Quarter Charge

Johnson & Johnson, the parent company of DePuy Orthopedics recently took a fourth quarter charge of over $3 billion dollars related primarily to their voluntary recall artificial hip implants—the DePuy ASR Acetabular System and the ASR Hip Resurfacing System.
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