FDAApril 16, 2018device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There may be burrs on the extraction hole threads.

What to do

FDA enforcement status: Terminated

Brands named

depuy orthopaedicsdepuy

UPCs

10603295042280

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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ATTUNE Revision CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Implant, Knee — Recall Details · AllClear