FDAApril 28, 2017device

FEM IM NAIL 14MMDX30CM LEFT, FEM IM NAIL 14MMDX30CM RIGHT FEM IM NAIL 13MMDX32CM LEFT FEM IM NAIL 14MMDX32CM LEFT FEM IM NAIL 13MMDX32CM RIGHT FEM IM NAIL 14MMDX32CM RIGHT FEM IM NAIL 11MMDX34CM LEFT FEM IM NAIL 13MMDX34CM LEFT FEM IM NAIL 14MMDX34CM LEFT FEM IM NAIL 11MMDX34CM RIGHT FEM IM NAIL ...

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

The hazard

Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

002257300040022573001400225732003002257320040022573201300225732014002257340010022573400300225734004002257340110022573401300225734014

Recall history

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

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