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  2. 2010 DePuy Hip Recall - Wikipedia

    en.wikipedia.org/wiki/2010_DePuy_Hip_Recall

    The 2010 DePuy Hip Replacement Recall was instituted when DePuy Orthopaedics, Inc., a division of Johnson and Johnson, recalled its ASR XL Acetabular metal-on-metal hip replacement system on August 24, 2010.

  3. DePuy Synthes - Wikipedia

    en.wikipedia.org/wiki/DePuy_Synthes

    On August 24, 2010, DePuy recalled all ASR hip implant systems sold since 2003. The 2010 DePuy Hip Recall was issued after research released by the National Joint Registry (NJR) found high rates of hip replacement failure for the ASR XL Acetabular and ASR Hip Resurfacing systems.

  4. Hip replacement - Wikipedia

    en.wikipedia.org/wiki/Hip_replacement

    A total hip replacement (total hip arthroplasty or THA) consists of replacing both the acetabulum and the femoral head while hemiarthroplasty generally only replaces the femoral head. Hip replacement is one of the most common orthopaedic operations, though patient satisfaction varies widely.

  5. J&J Adds Eprex Anemia Drug to Recall Tally - AOL

    www.aol.com/2011/09/26/jj-adds-eprex-anemia-drug...

    Its DePuy division's recall of faulty hip-replacement devices has touched off thousands of patient lawsuits; J&J has set aside at least $922 million to cover litigation costs.

  6. Hip resurfacing - Wikipedia

    en.wikipedia.org/wiki/Hip_resurfacing

    The hip resurfacing devices are metal-on-metal articulating devices which differ from total hip replacement devices because they are more bone conserving and retain the natural geometry (so-called large ball THR devices share this trait).

  7. Philips shares surge on US recall settlement news - AOL

    www.aol.com/news/philips-pays-1-1-billion...

    The devices were recalled because of concerns that foam used in them could degrade and become toxic, carrying potential cancer risks. CEO Roy Jakobs declined to say whether the bill was smaller...

  8. US FDA identifies recall of Philips medical imaging devices ...

    www.aol.com/news/us-fda-identifies-recall...

    Philips was recalling some models of the Panorama 1.0T HFO device in the U.S. due to risk of explosion during a "quench procedure" caused by excessive buildup of helium gas.

  9. Metallosis - Wikipedia

    en.wikipedia.org/wiki/Metallosis

    DePuy hip replacement recall. In August 2010, DePuy recalled its hip replacement systems ASR XL Acetabular Hip Replacement System and ASR Hip Resurfacing System due to failure rates and side effects including metallosis.

  10. Johnson & Johnson - Wikipedia

    en.wikipedia.org/wiki/Johnson_&_Johnson

    On August 24, 2010, DePuy, a subsidiary of American giant Johnson & Johnson, recalled its ASR (articular surface replacement) hip prostheses from the market. DePuy said the recall was due to unpublished National Joint Registry data showing a 12% revision rate for resurfacing at five years and an ASR XL revision rate of 13%.

  11. Minimally invasive hip resurfacing - Wikipedia

    en.wikipedia.org/wiki/Minimally_invasive_hip...

    Minimally invasive hip resurfacing (MIS) is a total or partial hip surgery that can be carried out through an incision of less than 10 cm (4 inches) without imparting great forces on the anatomy or compromising component positioning.