Z-0631-2022 Class II Terminated

Recalled by DePuy Orthopaedics, Inc. — Warsaw, IN

Recall Details

Product Type
Devices
Report Date
February 16, 2022
Initiation Date
January 5, 2022
Termination Date
December 22, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
6 units

Product Description

ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154909003

Reason for Recall

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.

Distribution Pattern

US Nationwide distribution in the states of TN, TX.

Code Information

Lots: JH9651, JH9649 GTIN: 10603295383178