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Zimmer Biomet, Inc. recalls 14-442000S Antegrade Femoral Nail Instrument Kit, orthopedic instrument
Recalled March 7, 2018 · FDA recall Z-0774-2018 · Zimmer Biomet
Hazard
Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail. · FDA Class II
Units
337 total
Sold at
Distribution includes US Nationwide.
Description
Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
Product
14-442000S Antegrade Femoral Nail Instrument Kit, orthopedic instrument
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →