FDAFebruary 14, 2022device

BIOMET Trauma, [Item # 13182-22-26, DVR CROSSLOCK EXTRA LONG PLATE LEFT], [Item # 1318-12-126, DVR CROSSLOCK EXTRA LONG PLATE RIGHT], [Item # 1318-12-176, DVR CROSSLOCK EXTRA EXTRA LONG PLATE RIGHT]. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropr...

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

The hazard

Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgical intervention, and/or extension of surgery to find another part.

What to do

FDA enforcement status: Terminated

Brands named

biomet

UPCs

008878684461910088786844620700887868446313

Recall history

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

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