High Frequency Resection Electrodes — Class II medical device recall Z-2629-2017
Terminated recall by Olympus Corporation of the Americas, reported 2017-07-05, distributed nationwide. Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes.
| Recall number | Z-2629-2017 |
|---|---|
| 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 | 2017-04-19 |
| Classified | 2017-06-26 |
| Reported by FDA | 2017-07-05 |
| Terminated | 2018-10-01 |
| Distributed | Nationwide (US) |
| Quantity | 1,264 units |
| Lot numbers | 16123P03L001, 16124P03L001, 16131P03L001, 16139P03L001, 16140P03L001, 16144P03L001, 16144P03L002, 16144P03L003, 16155P03L001, 16169P03L001, 16173P03L001, 16174P03L001, 16174P03L002, 16195P04L001, 16215P04L001, 16223P03L001, 16224P03L001, 16236P03L001, P16X0001, P16X0002, P16X0003, P16X0004, P16Y0001, P16Y0002, P16Y0003, P16Y0004, P16Y0005, P16Y0006, P16Y0007, P16Z0001, P16Z0002, P16Z0003, P1710001, P1720001, P1720002 |
| Model numbers | A22201C, WA22037C |
Product
High Frequency Resection Electrodes, endoscope, ac-powered and accessories The electrodes are used for endoscopic diagnosis and treatment in urological and gynecological applications.
Reason for recall
Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes.
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-2629-2017. 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.