Class II

Medical Device Recall: MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;

Medtronic MiniMed, Inc. · July 13, 2026

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.

Distribution

International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.

Quantity Affected

7

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2981-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.