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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


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

New London:
504 W. Water Street
New London, WI 54961

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