FDA Device recall Z-1017-2016
Synthes Small Electric Drive (SED)
- FDA Device
- Class II
- ongoing
- Published 2016-03-02
On 2016-03-02 the FDA classified a Class II recall of Synthes Small Electric Drive (SED) by The Anspach Effort, citing may operate solely in reverse mode, not operate in reverse mode when intended, not function or an unintentionally start.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1017-2016 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2014-11-14 |
| Published | 2016-03-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | The Anspach Effort |
| Distribution | AR, AZ, CA, CO, FL, HI, ID, IL, KS, LA, MI, NC, NY, TX, VA, WA |
Product
Synthes Small Electric Drive (SED)
Reason
May operate solely in reverse mode, not operate in reverse mode when intended, not function or an unintentionally start.
Identifiers
| code_info | All lots from production launch |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1017-2016%22
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