Infusion Pump
- Recalling firm
- Medtronic New Zealand Limited
- Product
- INFUSION PUMP. [Device]. Model: MiniMed™ Paradigm™ Insulin Pumps (all models); 670G Insulin Pumps (all models); 700G Insulin Pumps (all models); 780 Insulin Pumps (all models). Also covers: MiniMed DIB - 670G; MiniMed 700G series Pumps; MiniMed DIA - 780G pump
- Reason
- 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...
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-03-18
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/279928f0-b847-458b-8bbe-cb118eb3cedb