PlainRecalls
FDA Devices Moderate Class II Terminated

ATTUNE Revision CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Implant, Knee

Reported: May 16, 2018 Initiated: April 16, 2018 #Z-1704-2018

Product Description

ATTUNE Revision CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Implant, Knee

Reason for Recall

There may be burrs on the extraction hole threads.

Details

Recalling Firm
DePuy Orthopaedics, Inc.
Units Affected
1 unit
Distribution
The products were distributed to the following US states: FL, MO, and PA.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
ATTUNE Revision CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Implant, Knee. Recalled by DePuy Orthopaedics, Inc.. Units affected: 1 unit.
Why was this product recalled?
There may be burrs on the extraction hole threads.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 16, 2018. Severity: Moderate. Recall number: Z-1704-2018.