Recall Z-2981-2026— Medtronic MiniMed, Inc.
Class II · Ongoing
Class II FDA medical device recall by Medtronic MiniMed, Inc., initiated 2026-07-13. FDA's recall record names no specific 510(k) clearance for this event. Product: MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;. Reason: Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis..
- Recalling firm
- Medtronic MiniMed, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-07-13
- Firm location
- Northridge, CA, United States
Product description
MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
Reason for recall
Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.
Data sourced from openFDA. This site is unofficial and independent of the FDA.