FDA Device recall Z-0754-2017
HF Cable WA00014A, Endoscopic electrosurgical unit and accessories
- FDA Device
- Class II
- terminated
- Published 2016-12-21
On 2016-12-21 the FDA classified a Class II recall of HF Cable WA00014A, Endoscopic electrosurgical unit and accessories by Olympus, citing software malfunction that results in incorrect generation or display of error codes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0754-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-03 |
| Published | 2016-12-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Olympus |
| Distribution | US |
Product
HF Cable WA00014A, Endoscopic electrosurgical unit and accessories
Reason
Software malfunction that results in incorrect generation or display of error codes.
Identifiers
| code_info | Model Number: WA00014A Lot Numbers: 158W, 159W, 15XW, 15YW, 15ZW, 161W, 162W, 163W, 164W, 165W, 166W, 167W |
|---|
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-0754-2017%22
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