FDAJanuary 11, 2016device

LPS-FLEX GSF OPT prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer Various sizes¿ Product Usage "" This device is indicated for patients with severe knee pain and disability due to: Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis. Co...

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

00576401351005764013520057640145100576401452005764015510057640155200576401651005764016520057640175100576401752

Recall history

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

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