Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29716 |
| Brand Name: | NMD - Vanta™ with AdaptiveStim™ Neurostimulator System |
| Model: | A71200: Vanta Clinician Programmer Application (CP App) |
| Affected: | |
| Software version: | v2.0.2455 |
| 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: | The manufacturer has identified a potential communication issue in which the Vanta™ Clinician Programmer Application (CP App) A71200 v2.0.2455 may be unable to connect with a Vanta™ Implantable Neurostimulator (INS) Model 977006 when a patient is implanted with more than one (1) neurostimulator.The manufacturer has made available the new software version for the Vanta CP App A71200 (v2.0.2465) to address this issue. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 8/12/2022 |
