Uretero-reno fiberscope URF-P6RP6 recall
Uretero-reno fiberscope URF-P6RP6
Why was Uretero-reno fiberscope URF-P6RP6 recalled?
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 fiberscope URF-P6RP6
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 2399
- Distribution
- US Nationwide. Canada and Mexico
- Recall date
- August 1, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)