FDADecember 12, 2017device

PERSONA¿ THE PERSONALIZED KNEE SYSTEM "PSN TIB STM 5 DEG SZ D R" indicated for patients with severe knee pain and disability due to: - Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis.

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

The hazard

A complaint was received for Item 42-5320-067-02, lot 63236047. It was report that there was no set screw or taper plug included in the box. Complaint investigation confirmed that the entire lot of 63236047 was missing the set screw and taper plug.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

42532006702

Recall history

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

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