FDAMarch 28, 2024device

NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.

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

The hazard

Out of specification violation of devices that results in a gap existing within the fixture that presses the fiber metal pad to the substrate, causing the pad to not fully bond to the substrate.

What to do

FDA enforcement status: Ongoing

Brands named

zimmer

UPCs

0059520150100595201502005952015050059520150600889024207806008890242077900088902420781300889024207820

Recall history

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

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