FDAFebruary 27, 2025device

NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis, Model Number 00-5962-042-10

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

The hazard

The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label does not match with the compatibility statements "USE WITH PLATE 5, 6" in the translations section of the same label.

What to do

FDA enforcement status: Ongoing

Brands named

zimmer

UPCs

0088902466621400596204210

Recall history

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

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