FDA Device recall Z-0747-2016
Synthes Small Electric Drive (SED). For use in general traumatology
- FDA Device
- Class II
- terminated
- Published 2016-02-10
On 2016-02-10 the FDA classified a Class II recall of Synthes Small Electric Drive (SED). For use in general traumatology by The Anspach Effort, citing the affected Small Electric Drive (SED) may operate solely in reverse mode, not operate in reverse mode when intended, not function, or unintentionally start.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0747-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-08-14 |
| Published | 2016-02-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | The Anspach Effort |
| Distribution | US |
Product
Synthes Small Electric Drive (SED). For use in general traumatology.
Reason
The affected Small Electric Drive (SED) may operate solely in reverse mode, not operate in reverse mode when intended, not function, or unintentionally start.
Identifiers
| code_info | All Lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0747-2016%22
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