Bronchofiberscope BF-40 recall
Bronchofiberscope BF-40
Why was Bronchofiberscope BF-40 recalled?
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.
What should I do if I have this product?
Review the official FDA enforcement record for current 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 lot codes
- Product
- Bronchofiberscope BF-40
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 1347
- Distribution
- The products were distributed US nationwide and Canada.
- Recall date
- October 10, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)