DePuy Orthopaedics, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0631-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: January 5, 2022

Date Posted: February 16, 2022

Recall Number: Z-0631-2022

Event ID: 89454

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.

Status: Terminated

Product Quantity: 6 units

Code Information:

Lots: JH9651, JH9649 GTIN: 10603295383178

Distribution Pattern:

US Nationwide distribution in the states of TN, TX.

Voluntary or Mandated:

Voluntary: Firm initiated