Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23248 |
| Brand Name: | Vygon GmbH - catheter |
| Model: | |
| Affected: | Product code - VY-1261.153, Vy-1261.203, VY-1261.205, VY-1261.207, VY-1261.306 |
| Software version: | |
| Recalling Organisation: | Device Technologies New Zealand 47 Arrenway Drive Albany AUCKLAND 0632 |
| Contact Information: | 09 913 2000 |
| Manufacturer: | Vygon GmbH & Co KG |
| Issue: | The manufacturer would like to highlight to users the revised Instructions for Use (IFU) concerning the removal of the Stylet |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 28/6/2018 |
