FDANovember 29, 2017device

NEXGEN GSF POROUS FEMORAL LPS FLEX SIZE F, RIGHT¿ " These devices are indicated for patients with: - Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis. - Previous tibial condyle or plateau fractures with loss of anatomy or function. - Varus or valgus deformities. -...

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

00576201652

Recall history

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

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