FDAJanuary 11, 2016device

PRCT MIS CR MOB PLT prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing various sizes This device is indicated for patients with severe knee pain and disability due to: Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis. Collagen disorders,...

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

The hazard

LDPE bag containing the implant adheres to the highly polished implant surface.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

005930010010059300100200593002001005930020020059300300100593003002005930040010059300400200593004041005930040420059300500100593005002

Recall history

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

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