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FDASeptember 9, 2021device

ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001

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

The hazard

Packaging may include screws that are not intended to be used with the 5mm augments, may cause delay in surgery

What to do

FDA enforcement status: Terminated

Brands named

depuy orthopaedicsdepuy

UPCs

10603295057642

Recall history

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

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