EVIS EXERA III Bronchovideoscope recall
EVIS EXERA III Bronchovideoscope
Why was EVIS EXERA III Bronchovideoscope recalled?
The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.
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?
UDI-DI: 04953170342134; Serial No. 2911858; Model No. BF-XP190.
- Product
- EVIS EXERA III Bronchovideoscope
- Recalling firm
- Aizu Olympus Co., Ltd.
- Distribution
- US Nationwide distribution in the states of FL, IL, NC, PA & TX.
- Recall date
- August 31, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)