Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 36598 |
| Brand Name: | INFUSION PUMP |
| Model: | MiniMed™ Paradigm™ Insulin Pumps (all models) |
| 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 MiniMed |
| Brand Name: | MiniMed DIB - 670G |
| Model: | 670G Insulin Pumps (all models) |
| 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 MiniMed |
| Brand Name: | MiniMed 700G series Pumps |
| Model: | 700G Insulin Pumps (all models) |
| 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 MiniMed |
| Brand Name: | MiniMed DIA - 780G pump |
| Model: | 780 Insulin Pumps (all models) |
| 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 MiniMed |
| Issue: | Due to environmental conditions, there may be slight variability in the amount of insulin delivered when the pump is worn at distances above or below the location of the infusion set. This variability may increase with increasing distances above or below the infusion set location. Placing the pump above the infusion site can cause over-delivery and placing it below your infusion site can cause under-delivery. The greatest variability in insulin delivery may occur at distances beyond 35.5 cm above or below the infusion set location. This variability in insulin delivery will not be captured in the pump's history or CareLink reports. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 18/3/2026 |
