FDAClass IIMay 25, 2022

Olympus Uretero-reno videoscope recall

Olympus Uretero-reno videoscope, Model No. URF-V2

Why was Olympus Uretero-reno videoscope recalled?

The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.

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?

1 unit, serial number 2825505F UDI 04953170343582

Product
Olympus Uretero-reno videoscope, Model No. URF-V2
Recalling firm
Olympus Corporation of the Americas
Quantity
1
Distribution
US Nationwide distribution in the state of AZ.
Recall date
May 25, 2022
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls