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FDA (Device enforcement)Recalled 2026-07-13class ii

Medtronic MiniMed, Inc.: MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;

Is my product affected?

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

  • UPC 00763000404536
  • UPC 00763000404543

Check against the official notice below — it lists the full affected range.

What happened

Medtronic MiniMed is recalling seven loaner insulin pumps (MiniMed 670G models MMT-1781 and MMT-1782) distributed internationally to Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, and Northern Ireland. These pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad and allow moisture to enter the device.

The potential damage from moisture intrusion could result in insulin over- or under-delivery, which may cause hypoglycemia (low blood sugar), hyperglycemia (high blood sugar), or diabetic ketoacidosis. The recall affects six specific serial numbers for model MMT-1781 and one for model MMT-1782. The source does not specify what remedy consumers should take.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

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.

Details from the source

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: 7 Lot/code info: Model/UDI-DI Serial Numbers: MMT-1781/00763000404536/NG2665223H, NG2748200H, NG2748664H, NG2755237H, NG2716176H, NG3547582H. MMT-1782/00763000404543/NG2768190H

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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