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FDADecember 21, 2018device

Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766

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

The hazard

Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

00880304434349

Recall history

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

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