FDA Device recall Z-1559-2022
EVIS EXERA III Bronchovideoscope
- FDA Device
- Class II
- terminated
- Published 2022-08-31
On 2022-08-31 the FDA classified a Class II recall of EVIS EXERA III Bronchovideoscope by Aizu Olympus, citing the recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1559-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-07-20 |
| Published | 2022-08-31 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Aizu Olympus |
| Distribution | US |
Product
EVIS EXERA III Bronchovideoscope
Reason
The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.
Identifiers
| code_info | UDI-DI: 04953170342134; Serial No. 2911858; Model No. BF-XP190. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1559-2022%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.