Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 27160 |
| Brand Name: | CN - Intellis Implantable Neurostimulator 97716 |
| Model: | Model Numbers - 97715- 97716- 97725 |
| Affected: | |
| 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: | The manufacturer has received reports between January 2020 and November 24, 2020 where users encountered this validation error followed by a system error on the CT900 Clinician Programmer A710 Intellis Software Application version 1.3.80 indicating that the stimulator programming update could not be completed. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 15/1/2021 |
