Olympus ENDOEYE HD II Rigid Videoscope Catalog Numbers: WA50040A — Class II medical device recall Z-0697-2024
Ongoing recall by Olympus Corporation of the Americas, reported 2024-01-17, distributed nationwide. Reports of a pink or green coloration of the image. If the issue is encountered during a procedure, device exc
| Recall number | Z-0697-2024 |
|---|---|
| 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 | 2023-11-06 |
| Classified | 2024-01-10 |
| Reported by FDA | 2024-01-17 |
| Distributed | Nationwide (US) |
| UPC / GTIN / UDI-DI | 04042761074964, 04042761074971 |
| Model numbers | WA50040A, WA50042A |
Product
Olympus ENDOEYE HD II Rigid Videoscope Catalog Numbers: WA50040A, WA50042A -used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery within the thoracic and abdominal cavities including the female reproductive organs.
Reason for recall
Reports of a pink or green coloration of the image. If the issue is encountered during a procedure, device exchange could potentially result in prolonged surgery; potential visual impacts mucosal injury or bleeding may occur.
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-0697-2024. 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.