DePuy Orthopaedics, Inc.: Medical Device Recall in 2018 - (Recall #: Z-1703-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 16, 2018

Date Posted: May 16, 2018

Recall Number: Z-1703-2018

Event ID: 79818

Reason for Recall:

There may be burrs on the extraction hole threads.

Status: Terminated

Product Quantity: 2 units

Code Information:

Lot Number HC1179, GTIN Number 10603295042181; Lot Number HC1183, GTIN Number 10603295042181

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated