FDA Device recall Z-3288-2018
Bronchovideoscope F-1TQ180
- FDA Device
- Class II
- terminated
- Published 2018-10-10
On 2018-10-10 the FDA classified a Class II recall of Bronchovideoscope F-1TQ180 by Olympus, citing the attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrume….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3288-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-08-08 |
| Published | 2018-10-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Olympus |
| Distribution | US |
Product
Bronchovideoscope F-1TQ180
Reason
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
Identifiers
| code_info | all lot codes |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3288-2018%22
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