Olympus Bronchovideoscope BF Type recall
Olympus BRONCHOVIDEOSCOPE BF Type, Model Numbers BF-P150, BF-1T150
Why was Olympus Bronchovideoscope BF Type recalled?
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
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?
All serial numbers BF-P150* BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 UDI: 04953170288876 BF-1T150 BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 UDI: 04953170288968
- Product
- Olympus BRONCHOVIDEOSCOPE BF Type, Model Numbers BF-P150, BF-1T150
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 9 units
- Distribution
- US Nationwide Distribution.
- Recall date
- July 26, 2023
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)