OES Bronchofiberscope Olympus BF Type P60 recall
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60
Why was OES Bronchofiberscope Olympus BF Type P60 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-P60; UDI: 4953170339196; All Serial No.
- Product
- OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 1,007 units US; 5,443 units OUS
- Distribution
- US Nationwide Distribution.
- Recall date
- October 22, 2025
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)