FDAApril 17, 2020device

Knee Products: US154709 Knees Vanguard M Partial Knee System MonoBlock Tibial Tray, Right Medial/Left Lateral, B8 US154722 Knees Vanguard M Partial Knee System MonoBlock Tibial Tray, Left Medial/Right Lateral, D5 US154725 Knees Vanguard M Partial Knee System MonoBlock Tibial Tray, Right Medial/Le...

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

The hazard

Potential presence of elevated endotoxin levels that exceed the specification limit

What to do

FDA enforcement status: Terminated

Brands named

biomet

UPCs

008803041807030088030418083300880304180864008803041806660088030418068000880304180741008803041808020088030418081900880304180826008803041808400088030418088800880304180925

Recall history

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

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