Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29715 |
| 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: | As previously communicated by the manufacturer, in July 2022, in these rare occurrences during initial programming, the Vanta CP App will display the Error Code 1502 message because the Vanta INS Reset Block ID log is full. Once the log is full, all subsequent interrogations with the affected device will not be possible. So the manufactuere performed an INS diagnostic and log reset, which enabled the Vanta INSs to be interrogated by the Vanta CP App and complete programming. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 8/12/2022 |
