DePuy Orthopaedics, Inc. recalls ATTUNE Revision CRS Femoral LT SZ 5 Cemented, Catalog No. 150440105, Femoral Revision Implant, Knee

Recalled May 16, 2018 · FDA recall Z-1703-2018 · DePuy Orthopaedics

Hazard

There may be burrs on the extraction hole threads. · FDA Class II

Units

2 units

Sold at

The products were distributed to the following US states: FL, MO, and PA.

Description

There may be burrs on the extraction hole threads.

Product

ATTUNE Revision CRS Femoral LT SZ 5 Cemented, Catalog No. 150440105, Femoral Revision Implant, Knee

Manufacturer(s)

DePuy Orthopaedics, Inc.

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