HF Resection Electrodes — Class II medical device recall Z-0424-2023
Ongoing recall by Olympus Corporation of the Americas, reported 2022-12-14, distributed nationwide. An incompatible HF cable may be packaged with the HF Resection Electrodes. This cable cannot be connected to t
| Recall number | Z-0424-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Olympus Corporation of the Americas, Center Valley, PA, United States |
| Recall initiated | 2022-11-04 |
| Classified | 2022-12-07 |
| Reported by FDA | 2022-12-14 |
| Distributed | Nationwide (US) |
| UPC / GTIN / UDI-DI | 14042761085127, 14042761085134, 14042761085172, 14042761085301 |
| Lot numbers | 1000080316, 1000090824, 1000092201, 1000092202, WA22602S, WA22603S, WA22621S, WA22657S |
| Model numbers | WA22602S, WA22603S, WA22621S, WA22657S |
Product
HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S
Reason for recall
An incompatible HF cable may be packaged with the HF Resection Electrodes. This cable cannot be connected to the electrosurgical generator and may lead to delay or cancellation of the surgical procedure.
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-0424-2023. 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.