Mark S. Cornwall
Attorney and Counselor of Law
Use the form below to contact Mark Cornwall:

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Which DePuy device did you have implanted?*
Date DePuy device was implanted:*

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Please explain a little of the symptoms causing
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Have you had a chance to speak with your surgeon
about the effects of the recall?*
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If yes, what is the prognosis?*
Have you had your DePuy device already replaced by
a second surgery?*
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Have you been contacted by DePuy's insurance
company known as BROADSPIRE?*
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Have you signed their medical records
authorization?*
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you?*
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News and Updates
10.21.2010
This alert is to help those people who have been victimized, or will be victimized, by a failed hip surgery replacement implant from 2003 to the present. By letter dated Aug. 24, 2010, DePuy Orthopeadics, a subsidiary of Johnson & Johnson, recalled 93,000 defective implants on a so-called voluntary basis.

The two hip replacement devices recalled are known as the ASR Hip Recurring System and the ASR XL Acetabluor System, commonly referred to as ASR. According to a source...

08.27.2010
More than two years after the Food and Drug Administration began receiving complaints about the failure of a hip replacement implant made by the DePuy Orthopaedics unit of Johnson & Johnson, the company said Thursday that it was recalling two kinds of hip implants.

DePuy said that it had made the decision to withdraw the products because...