FDA Device recall Z-2015-2023
Olympus BRONCHOVIDEOSCOPE, Model Numbers BF-Q170
- FDA Device
- Class I
- ongoing
- Published 2023-07-26
On 2023-07-26 the FDA classified a Class I recall of Olympus BRONCHOVIDEOSCOPE, Model Numbers BF-Q170 by Olympus, citing there have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2015-2023 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-06-08 |
| Published | 2023-07-26 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Olympus |
| Distribution | US |
Product
Olympus BRONCHOVIDEOSCOPE, Model Numbers BF-Q170
Reason
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Identifiers
| code_info | All serial numbers BF-Q170 BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 UDI: 04953170342912 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2015-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.