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FDASeptember 28, 2016device

Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Complaints have been reported that the handpiece is inoperable. The investigation found that the complaints were related to the lack of preventative maintenance contrary to what is recommended in the instructions for use included with the handpiece. An inoperable device may lead to a delay in surgery

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

00592704000

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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