Toney Law Offices SC
CALL US TODAY (800)924-6366
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
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 WisconsinCall: 1-800-924-6366
CONTACT INFORMATION
Toney Law Offices SC
Steven L. Toney, Attorney
Toll Free: 800-924-6366
New London:
920-982-6366
504 W. Water Street
New London, WI 54961
