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FDANovember 29, 2017device

LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT LPS POROUS FEM SIZE F-RT This device is indicated for patients with severe knee pain and disability

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

The hazard

The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

005990014020059900150200599201602

Recall history

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

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LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT LPS POROUS FEM SIZE F-RT This device is indicated for patients with severe knee pain and disability — Recall Details · AllClear