DePuy Orthopaedics, Inc. recalls ATTUNE REVISION CEMENTED STEM 16X80MM-intended for use in total knee arthroplasty Part Number: 1512-16-080

Recalled September 1, 2021 · FDA recall Z-2348-2021 · DePuy Orthopaedics

Hazard

Package labeled as 16mm x 80mm contained a 16mm x 130mm stem instead and result in obtaining a replacement · FDA Class II

Units

7 units

Sold at

International distribution in the countries of Canada, France.

Description

Package labeled as 16mm x 80mm contained a 16mm x 130mm stem instead and result in obtaining a replacement

Product

ATTUNE REVISION CEMENTED STEM 16X80MM-intended for use in total knee arthroplasty Part Number: 1512-16-080

Manufacturer(s)

DePuy Orthopaedics, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →