BF-1TQ180: EVIS EXERA II Bronchovideoscope recall
BF-1TQ180: EVIS EXERA II Bronchovideoscope
Why was BF-1TQ180: EVIS EXERA II Bronchovideoscope recalled?
Bronchofiberscope Updated instructions on the use of certain chemicals to be used for reprocessing, conditions for ETO gas sterilization, rinsing steps after high-level disinfection, and a recommendation on using sterilization
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. UDI: 04953170339349
- Product
- BF-1TQ180: EVIS EXERA II Bronchovideoscope
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 242 units
- Distribution
- US Nationwide distribution.
- Recall date
- May 18, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)