FDA Device recall Z-2243-2013
Synthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile
- FDA Device
- Class II
- terminated
- Published 2013-09-25
On 2013-09-25 the FDA classified a Class II recall of Synthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile by Synthes Usa Hq, citing firm discovered that a nail that was within the scope of a previous Trauma Nail recall had been distributed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2243-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-04-18 |
| Published | 2013-09-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Synthes Usa Hq |
| Distribution | MA |
Product
Synthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile. Orthppedic implant device.
Reason
Firm discovered that a nail that was within the scope of a previous Trauma Nail recall had been distributed.
Identifiers
| code_info | Part Number 450.851S, Lot Number 7065061 |
|---|
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-2243-2013%22
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