DePuy Orthopaedics, Inc.: Medical Device Recall in 2021 - (Recall #: Z-0074-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 9, 2021

Date Posted: October 13, 2021

Recall Number: Z-0074-2022

Event ID: 88722

Reason for Recall:

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

Status: Terminated

Product Quantity: 10 units

Code Information:

Lot Number: J6304Z GTIN: 10603295057642

Distribution Pattern:

US Nationwide distribution in the states of CA, LA, MN, MO, NC, NE, OR, PA, WA, WI.

Voluntary or Mandated:

Voluntary: Firm initiated