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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. [1] [2]
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).
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.
Older adults are catching up on missed hip and knee replacements and other non-urgent surgeries, a shift that will benefit medical device makers this year, Wall Street analysts said after...
Hip resurfacing, sometimes called hip shaving, is preferred over a total hip replacement for elite athletes, Su said, because it preserves more of the femur, uses a metal alloy made of cobalt...
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.
On August 24, 2010, DePuy recalled [4] 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.
Alec Baldwin underwent hip replacement surgery after suffering 'very intense chronic pain,' his wife, Hilaria, said in a Tuesday Instagram post.
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.
The documentary explores the FDA's 510(k) process which allows a medical device to be fast-tracked onto the market with less clinical study and human testing. The film also explores problems with hip replacement devices that can lead to cobalt poisoning and vaginal mesh devices that injured multiple women.