ZNN Antegrade Femoral Nail — Class II medical device recall Z-2060-2015
Terminated recall by Zimmer, Inc., reported 2015-07-22, distributed in AK, NC. A single distributed ZNN Greater Trochanter Femoral Nail may have been dented. Potential for fatigue of implan
| Recall number | Z-2060-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2015-06-17 |
| Classified | 2015-07-13 |
| Reported by FDA | 2015-07-22 |
| Terminated | 2016-03-15 |
| Distributed | AK, NC |
| Countries outside the US | DE, JP, TW |
| Quantity | 8 |
| Reason classes | device malfunction |
| Lot numbers | 62763724 |
| Model numbers | 47-2492-320-10 |
Product
ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2060-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.