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Zimmer Biomet, Inc. recalls Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa, Model#14-442093 Antegrade Femoral Connecting Bolt.
Recalled March 7, 2018 · FDA recall Z-0773-2018 · 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 units
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
Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa, Model#14-442093 Antegrade Femoral Connecting Bolt. orthopedic instrument
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →