Olympus OES BRONCHOFIBERSCOPE BF Type — Class I medical device recall Z-2011-2023
Ongoing recall by Olympus Corporation of the Americas, reported 2023-07-26, distributed nationwide. There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchosco
| Recall number | Z-2011-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Olympus Corporation of the Americas, Center Valley, PA, United States |
| Recall initiated | 2023-06-08 |
| Classified | 2023-07-17 |
| Reported by FDA | 2023-07-26 |
| Distributed | Nationwide (US) |
| Quantity | 1,535 units |
| UPC / GTIN / UDI-DI | 04953170055980, 04953170339264, 04953170339288 |
| Model numbers | BF-1T60, BF-MP60, BF-P60, BF-XT40 |
Product
Olympus OES BRONCHOFIBERSCOPE BF Type, Model Numbers BF-XT40, BF-P60, BF-MP60, BF-1T60
Reason for recall
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
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-2011-2023. 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.