Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25200 |
| Brand Name: | TJF Duodenovideoscope |
| Model: | |
| Affected: | TJF-140R, TJF-160R, TJF-240 and JF-140R duodenoscope |
| 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 been made aware of an event where fraying elevator wires of the TJF-140R, TJF-160R, TJF-240 and JF-140R can occur. In an effort to mitigate potential risk to patient and staff health, the manufacturer has provided additional Instructions for safe use. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 11/10/2019 |
