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: Richmond Virginia Personal Injury LawyerYour Stryker Hip Implant Could be Defective
By Michael Phelan
According to an FDA Warning issued on November 28, 2007 and released to the public on January 15, 2008, some models of Stryker hip implants may be defective. The FDA has received numerous complaints concerning Stryker hip implants from patients experiencing fractures, pain, wear particles, fragments, and broached bones resulting in bone fractures. Many of these problems required revision surgery. This is the second stern warning issued in 2007 by the FDA to Stryker about its http://www.fda.gov/foi/warning_letters/s6627c.htmhip implants. The most recent warning letter followed an inspection by the FDA at Stryker's Mahwah, NJ plant which took place on June 12 and July 1, 2007.
Full post as published by Richmond Virginia Personal Injury Lawyer on January 17, 2008 (boomark / email).
DePuy Metal Hip Replacement
alleging defective product recall of ASR hip implant for health reasons.
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allegedly recalled implant stimulators due to malfunction.
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alleging sterilization practices can cause implant failure.
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