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Taperloc Complete Micro Primary Femoral

Biomet Orthopedics, LLC · Model 51-107180 · UDI-DI 00880304513594

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510(k) clearances

138,209

Adverse events (388 deaths)

203

Recalls

Facilities

Recalls

Date	Firm	Reason
2023-10-09	Biomet, Inc.	Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
2023-10-09	Biomet, Inc.	Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
2023-10-09	Biomet, Inc.	Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
2023-10-09	Biomet, Inc.	Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
2023-10-09	Biomet, Inc.	Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
2023-10-09	Biomet, Inc.	Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
2023-10-09	Biomet, Inc.	Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
2023-10-09	Biomet, Inc.	Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
2023-10-09	Biomet, Inc.	Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
2023-10-09	Biomet, Inc.	Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery

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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.