EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V — Class II medical device recall Z-2467-2023
Ongoing recall by Olympus Corporation of the Americas, reported 2023-09-06, distributed nationwide. Recent reports of patient infection.
| Recall number | Z-2467-2023 |
|---|---|
| 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 | 2023-07-27 |
| Classified | 2023-08-28 |
| Reported by FDA | 2023-09-06 |
| Distributed | Nationwide (US) |
| Quantity | 6,426 units |
| UPC / GTIN / UDI-DI | 04953170405563 |
| Model numbers | TJF-Q190V |
Product
EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V
Reason for recall
Recent reports of patient infection.
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-2467-2023. 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.