EVIS EXERA III Colonovideoscope-For endoscopy and endoscopic surgery… — Class II medical device recall Z-1132-2023
Ongoing recall by Olympus Corporation of the Americas, reported 2023-02-22, distributed nationwide. A single CF-Q180AL colonovideoscope was utilized in a veterinary endoscopy procedure in advance of being assig
| Recall number | Z-1132-2023 |
|---|---|
| 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 | 2022-12-21 |
| Classified | 2023-02-13 |
| Reported by FDA | 2023-02-22 |
| Distributed | Nationwide (US) |
| Quantity | 1 units |
| Reason classes | microbial contamination |
| UPC / GTIN / UDI-DI | 04953170202315 |
| Serial numbers | 2807443, CF-Q180AL |
Product
EVIS EXERA III Colonovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum, sigmoid colon, colon, and ileocecal valve) Model/Serial: CF-Q180AL
Reason for recall
A single CF-Q180AL colonovideoscope was utilized in a veterinary endoscopy procedure in advance of being assigned to a medical facility as a service loaner in error, potential for microbial contamination
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-1132-2023. 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.