Sulzer Hip Implant Recall
On December 8, 2000, Sulzer
Orthopedics recalled its Inter-Op acetabular shell for hip implants sold
primarily in the U.S. after October, 1999, with a small number of lots
sold after July, 1997. Approximately 17,500 patients were affected by the
recall.
The hip implant part is the
acetabular "shell" that is implanted into the upper part of the
hip called the acetabulum. Normally, the bone would form an integrated
bond with the shell; however, it appears that bone does not always bond
with shells when the lubricant residue is present. Loosening
of the shell may occur.
According to company
tests a number of patients who received the shell during their total hip
replacement have experienced loosening of the shell. Sulzer states that
there are specific hip symptoms associated with this problem.
If you have pain in
your inner thigh or groin, pain when arising from a seated position or
pain with standing and weight bearing, you may want to consult with your
doctor.
We handle
personal injuries claims from defective recalled hip implants for clients
across the nation.
If
you want to preserve a potential legal claim for a defective hip implant
product you believe you received, you should contact an attorney
immediately, since all states have mandatory time periods in which
lawsuits must be filed; otherwise, your case may be forever barred.
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