Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21255 |
| Brand Name: | Medtronic CN - DBS Lead, Model 3389 |
| Model: | |
| Affected: | 3387, 3389 and 3391 Deep Brain Stimulation Lead Kits |
| 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 complaints from physicians reporting that the DBS depth stop did not adequately secure to the lead. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 28/3/2017 |
