Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
Reported: August 1, 2018 Initiated: January 17, 2018 #Z-2518-2018
Product Description
Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R
Reason for Recall
Potential breakage of the endoscope s insertion tube bending section during surgical procedures
Details
- Recalling Firm
- Olympus Corporation of the Americas
- Units Affected
- 2548
- Distribution
- US Nationwide and Canada
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R. Recalled by Olympus Corporation of the Americas. Units affected: 2548.
Why was this product recalled? ▼
Potential breakage of the endoscope s insertion tube bending section during surgical procedures
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 1, 2018. Severity: Moderate. Recall number: Z-2518-2018.
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