Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device. Recalled by Zimmer, Inc. Due to A single distributed ZNN Greater Trochanter Femoral Nail...
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, Inc. directly.
Affected Products
ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device.
Quantity: 8
Why Was This Recalled?
A single distributed ZNN Greater Trochanter Femoral Nail may have been dented. Potential for fatigue of implant prior to sufficient fracture healing, which may result in need for implant removal and revision of fracture fixation to assure proper healing and avoid fracture malunion or nonunion.
Where Was This Sold?
This product was distributed to 2 states: AK, NC
About Zimmer, Inc.
Zimmer, Inc. has 437 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report