Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 27295 |
| Brand Name: | CVG - APV - Valiant Navion Stent Graft |
| Model: | |
| Affected: | Multiple Product numbers |
| Software version: | |
| Recalling Organisation: | Medtronic New Zealand Limited Unit 16 Mezzanine Level 5 Gloucester Park Road Onehunga AUCKLAND |
| Contact Information: | 0800 377 807 |
| Manufacturer: | Medtronic Inc |
| Brand Name: | CVG - APV - Valiant Navion Stent graft - US |
| Model: | |
| Affected: | Multiple Product numbers |
| Software version: | |
| Recalling Organisation: | Medtronic New Zealand Limited Unit 16 Mezzanine Level 5 Gloucester Park Road Onehunga AUCKLAND |
| Contact Information: | 0800 377 807 |
| Manufacturer: | Medtronic Inc |
| Issue: | Update: The manufacturer is currently working to further investigate and assess the cause of the events observed with the Valiant Navion Thoracic Stent Graft. To date, the root cause analysis suggests a loss of suture integrity, which could lead to separation of the longitudinal seam of the stent graft or stent ring detachment from the surface of the graft fabric. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 2/6/2022 |
