FDAJanuary 11, 2016device

CR Flex GSF Precoat Fem Natural Knee GSF NP Flex Natural Knee GSF POR Flex Natural Knee GSM NP Flex Natural Knee GSM POR Flex prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer various sizes Components with CSTi porous coating are indicated for uncemented or ...

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

005410014010054100140200541001501005410015020054100160100541001602005410017010054100170200541001801005410018020054120140200541201501

Recall history

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

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CR Flex GSF Precoat Fem Natural Knee GSF NP Flex Natural Knee GSF POR Flex Natural Knee GSM NP Flex Natural Knee GSM POR Flex prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer various sizes Components with CSTi porous coating are indicated for uncemented or ... — Recall Details · AllClear