Olympus Cystonephrofiberscope recall
Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5
Why was Olympus Cystonephrofiberscope recalled?
Incorrect adhesive used to secure the diopter ring and nameplate ring. Improperly connected diopter ring may result in the loss of adjustment function leading to a blurred field of vision and unintentional contact with the patients body and in rare cases perforation in the urinary tract/renal pelvis.
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?
UDI-DI: 04953170339417 Serial Number: 2456630 7171632 2769732 W501648A 2355088 2557155 2972060
- Product
- Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 7 units
- Distribution
- CA FL MA MD MI NJ OH PR WI
- Recall date
- June 22, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)