medical Class II Updated 2022-02-16

DePuy Orthopaedics, Inc. recalls ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as

Recalled Product

ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154706001


Hazard / Issue

May have adhesive residue on the posterior surface of the femoral augment, if undetected prior to implantation, soft tissue irritation and/or infection may occur.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lots: JJ3389 GTIN: 10603295382775
View official government recall

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