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VANGUARD

Biomet Orthopedics, LLC · Model 32-360506 · UDI-DI 00880304516144

MBVJWH Prescription
1
510(k) clearances
163
Adverse events
1
Recalls
31
Facilities

Recalls

DateFirmReason
2012-11-15Biomet, Inc.Biomet investigation identified that the square end of the offset tibial tray adaptor locking insert is oversized and may not engage insert tool screwdriver. This could cause a p

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.