Official recall record
MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2026-07-13
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00763000404536
- Brand on record
- Medtronic MiniMed, Inc.
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-09-17.
Record last checked against the registry on 2026-09-17.
Other recalls from this brand
- 2026-07-13 · US FDA — Medical Devices
MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712; - 2026-07-13 · US FDA — Medical Devices
MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW - 2026-06-16 · US FDA — Medical Devices
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
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