FDAFebruary 22, 2021device

The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Usage: consists of multiple components intended to replace the femoral, tibial, and patellar articular surfaces of the knee joint.

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

The hazard

Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+) Tibial Bases due to potential damaged packaging. These implant components are utilized in Total Knee Arthroplasty. The affected tibial bases are designed to be used in cemented applications.

What to do

FDA enforcement status: Terminated

Brands named

depuy orthopaedicsdepuy

UPCs

1060329549215310603295492160106032954921771060329549218410603295492191

Recall history

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

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