HF Cable WA00014A — Class II medical device recall Z-0754-2017
Terminated recall by Olympus Corporation of the Americas, reported 2016-12-21, distributed nationwide. Software malfunction that results in incorrect generation or display of error codes.
| Recall number | Z-0754-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Olympus Corporation of the Americas, Center Valley, PA, United States |
| Recall initiated | 2016-11-03 |
| Classified | 2016-12-14 |
| Reported by FDA | 2016-12-21 |
| Terminated | 2019-02-06 |
| Distributed | Nationwide (US) |
| Quantity | 494 units |
| Reason classes | device malfunction, software |
| Lot numbers | 158W, 159W, 15XW, 15YW, 15ZW, 161W, 162W, 163W, 164W, 165W, 166W, 167W |
| Model numbers | WA00014A |
Product
HF Cable WA00014A, Endoscopic electrosurgical unit and accessories
Reason for recall
Software malfunction that results in incorrect generation or display of error codes.
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-0754-2017. 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.