Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22407 |
| Brand Name: | URF-V_Uretero-Reno Videoscope |
| Model: | |
| Affected: | URF-V2 Uretero-Reno Videoscope |
| Software version: | |
| Recalling Organisation: | Olympus (NZ) Ltd 15D Paul Matthews Road Albany Auckland |
| Contact Information: | 0508 659 6787 |
| Manufacturer: | Olympus Medical Systems Corporation |
| Brand Name: | Flexible Ureteroscope |
| Model: | |
| Affected: | URF-P6 Uretero-Reno Fiberscope. |
| Software version: | |
| Recalling Organisation: | Olympus (NZ) Ltd 15D Paul Matthews Road Albany Auckland |
| Contact Information: | 0508 659 6787 |
| Manufacturer: | Olympus Medical Systems Corporation |
| Issue: | The manufacturer has received a small number of adverse event reports for the URF-V2 associated with damage to the bending section. Further to the Safety Alert issued in December 2016, the manufacturer has modified the design of the bending section of the URF-V2 and URF-P6 to address any deficiencies. |
| Recall action type: | Recall |
| Recall action: | Product to be exchanged |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 22/12/2017 |
