Uretero-reno videoscope URF-V2 Uretero-reno videoscope recall
Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
Why was Uretero-reno videoscope URF-V2 Uretero-reno videoscope recalled?
Potential breakage of the endoscope s insertion tube bending section during surgical procedures
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 Serial Numbers
- Product
- Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 2548
- Distribution
- US Nationwide and Canada
- Recall date
- August 1, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)