Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the rework process for the April 17,...
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
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 460MM
Quantity: 638 units
Why Was This Recalled?
During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
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