Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa Recalled by Zimmer Biomet, Inc. Due to Fracture of the bolt connecting the insertion guide...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Biomet, Inc. directly.
Affected Products
Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa, Model#14-442093 Antegrade Femoral Connecting Bolt. orthopedic instrument
Quantity: 337 units
Why Was This Recalled?
Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Biomet, Inc.
Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report