DePuy Hip Implant Recall Lawyers

If you or a loved one have been injured or required revision surgery for a defective hip implant contact us or call toll free 1-800-448-0883 for a free consultation and case evaluation by our product liability lawyers.

On August 24, 2010, DePuy Orthopedics recalled its ASRTM XL Acetabular System (hip implant) and ASRTM Hip Resurfacing System. Recent data from the National Joint Registry of England and Wales indicated a higher than expected revision rate at five years. Specifically, the data showed that the five-year revision rate for ASRTM XL Acetabular System was approximately 12% and for ASRTM Hip Resurfacing System was approximately 13%. The revision rate was highest with ASRTM head sizes below 50 mm in diameter and among female patients.

DePuy is a unit of Johnson & Johnson. ASRTM XL Acetabular System has been used in the U.S. and worldwide since 2004. The recall means that patients who received an ASRTM XL Acetabular System hip implant will need additional testing, monitoring and potentially additional surgeries. The data showed that 1 in 8 would need a revision.

Symptoms related to the reported problems with the hip implants are as follows:
  • Pain and swelling
  • Clicking
  • Problems walking
  • Loosening (when the implant does not stay attached to the bone)
  • Fracture
  • Dislocation

If you have had a hip replacement and received an ASRTM XL Acetabular System (hip implant) or ASRTM Hip Resurfacing System contact us for a free case consultation and evaluation. Fleming | Nolen | Jez, L.L.P. has experience in medical device litigation.

DePuy Hip Implant Recall Lawyers

If you or a loved one have been injured or required revision surgery for a defective hip implant contact us or call toll free 1-800-448-0883 for a free consultation and case evaluation by our product liability lawyers.

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