EVIS EXERA III Bronchovideoscope — Class II medical device recall Z-1559-2022
Terminated recall by Aizu Olympus Co., Ltd., reported 2022-08-31, distributed nationwide. The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare
| Recall number | Z-1559-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aizu Olympus Co., Ltd., Aizuwakamatsu, Japan |
| Recall initiated | 2022-07-20 |
| Classified | 2022-08-19 |
| Reported by FDA | 2022-08-31 |
| Terminated | 2025-01-22 |
| Distributed | Nationwide (US) |
| UPC / GTIN / UDI-DI | 04953170342134 |
| Serial numbers | 2911858 |
| Model numbers | BF-XP190 |
Product
EVIS EXERA III Bronchovideoscope
Reason for recall
The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.
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-1559-2022. 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.