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Zimmer Recall

A hip implant may be recalled by the manufacturer for a number of reasons. If your hip implant is recalled, this does not necessarily mean that the implant needs to be removed and replaced. In some cases the recall recommends different or more frequent monitoring. It is important to discuss the reason for the recall with your orthopaedic surgeon to determine the most appropriate course of action.

Zimmer Durom® Acetabular Component

On July 22, 2008, there was a voluntary recall of the Zimmer Durom® Acetabular Component ("Durom Cup") because the instructions for use/surgical technique instructions were inadequate.

The reason for this voluntary recall was determined by the FDA as "MISBRANDING: Labeling False and Misleading". See the attached link. Class 2 Device Recall Durom cup


Helping Defective Hip Replacement Recipients In Wisconsin

Call: 1-800-924-6366

CONTACT INFORMATION

Toney Law Offices SC
Steven L. Toney, Attorney
Toll Free: 800-924-6366

Madison:
608-838-6366
2810 Crossroads Drive, Suite 4000
Madison, WI 53718

New London:
920-982-6366
315 Burton Rd.
New London, WI 54961









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