Evis Exera III Bronchovideoscope Olympus Bf-q190 recall
EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190
Why was Evis Exera III Bronchovideoscope Olympus Bf-q190 recalled?
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model No. BF-Q190; UDI: 4953170434792, 4953170335198; All Serial No.
- Product
- EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 916 units US; 1,402 units OUS
- Distribution
- US Nationwide Distribution.
- Recall date
- October 22, 2025
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)