Home › Zimmer GmbH › Fitmore® Hip Stem

Fitmore® Hip Stem

Zimmer GmbH · Model 01.00551.202 · UDI-DI 00889024281165

KWA JDI JDL KWL Prescription

510(k) clearances

138,209

Adverse events (388 deaths)

203

Recalls

Facilities

Description

Fitmore Hip Stem B, Size 2

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

Query this across every FDA database — by API.

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

Get your free API key Read the docs

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.