FDA Device recall Z-1049-2022
BF-1TQ180: EVIS EXERA II Bronchovideoscope
- FDA Device
- Class II
- ongoing
- Published 2022-05-18
On 2022-05-18 the FDA classified a Class II recall of BF-1TQ180: EVIS EXERA II Bronchovideoscope by Olympus, citing bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfecti….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1049-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-03-08 |
| Published | 2022-05-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Olympus |
| Distribution | US |
Product
BF-1TQ180: EVIS EXERA II Bronchovideoscope
Reason
Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization
Identifiers
| code_info | All serial numbers. UDI: 04953170339349 |
|---|
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-1049-2022%22
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