FDA Device recall Z-2060-2015
ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device
- FDA Device
- Class II
- terminated
- Published 2015-07-22
On 2015-07-22 the FDA classified a Class II recall of ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device by Zimmer, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2060-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-06-17 |
| Published | 2015-07-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer |
| Distribution | AK, NC |
Product
ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device.
Reason
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.
Identifiers
| code_info | Part 47-2492-320-10; lot 62763724 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2060-2015%22
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