DePuy Orthopaedics Inc., a division of Johnson & Johnson, issued a recall on its ASR XL Acetabular System (a hip socket used in traditional hip replacement surgery) and ASR Hip Resurfacing System (a partial hip replacement that involves placing a metal cap on the ball of the femur) – both of which have been used in hip replacement surgery.

Both hip replacement products have been recalled by the manufacturer from hospitals, surgeons, and patients because they have been linked to a high failure rate. The products also have the possibility to release high levels of metal ion into patients. Pain, swelling, problems walking, and other complaints were noted by the company according to CNN Money. The FDA has received about 300 complaints about the ASR line of hip replacement devices since 2008 and after more than two years the company issued a release that it was recalling the two types of hip replacements.

About 93,000 of these devices have been implanted worldwide, the New York Times reported in March 2010. Patients who have had the ASR line of hip replacement products have needed additional “revision” or secondary surgeries to replace these devices. The medical procedure is what is known as a “revision surgery” or “secondary surgery.” These “revision surgeries” or “secondary surgeries” can become very expensive and are painful procedures which could have been avoided had the hip replacement device not been marketed as potentially defective.

If you have suffered injury from the ASR hip replacement system, please contact our Columbus personal injury lawyers by filling out our contact form or calling us at (888) 880 – HURT (4878).