FDA·Medical devices·August 26, 2026

Medtronic MiniMed recalls MiniMed 780G, 670G and 640G insulin pumps over loaner pumps cleaned with wrong products

Loaner insulin pumps may have been cleaned with products that do not mix safely with them, which could damage the case or keypad, let moisture in, and cause too much or too little insulin, leading to hypoglycemia, hyperglycemia, or diabetic ketoacidosis.

What to do

The notice does not give instructions. Read the official notice for details.

Do not stop taking a prescribed medicine, or stop using a device you rely on, until you have talked to your pharmacist or doctor.

Recall details

Product
MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW; MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;; MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;
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.
Units
257; 7; 16
Where sold
International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.
FDA classification
Class II · Ongoing
Classified by FDA
August 18, 2026
Recall started
July 13, 2026
FDA enforcement report
August 26, 2026
Identifiers
  • Codes: Model/UDI-DI Serial Numbers: MMT-1885CLW/00763000442187, 00763000974374/NG3150737H, NG3155194H, NG3151561H, NG3154693H, NG3151716H, NG3153547H, NG3153637H, NG3155407H, NG3152666H, NG3155788H, NG3081975H, NG2901117H, NG3080842H, NG3081463H, NG3153416H, NG3081894H, NG3153781H, NG3155944H, NG3081982H, NG3081525H, NG3155909H, NG3090722H, NG3154897H, NG3088436H, NG3088708H, NG3090073H, NG3155908H, NG3150720H, NG3092957H, NG3128715H, NG3128784H, NG3152774H, NG3153929H, NG3514566H, NG3150780H, NG3151290H, NG3151508H, NG3507161H, NG3508693H, NG3081976H, NG3151460H, NG3152051H, NG3152085H, NG3152344H, NG3153213H, NG3152772H, NG3155586H, NG3150786H, NG3153214H, NG3153385H, NG3151840H, NG3082019H…
  • FDA recall number: Z-2982-2026
  • Codes: Model/UDI-DI Serial Numbers: MMT-1781/00763000404536/NG2665223H, NG2748200H, NG2748664H, NG2755237H, NG2716176H, NG3547582H. MMT-1782/00763000404543/NG2768190H
  • FDA recall number: Z-2981-2026
  • Codes: Model/UDI-DI/Serial Numbers: MMT-1711/00763000404550/NG2660048H, NG2663343H, NG3015306H; MMT-1712/00763000404567/NG2628486H, NG2758213H, NG2999651H, NG3349198H, NG3351719H, NG2678842H, NG2831821H, NG2831546H, NG2932027H, NG3049657H, NG3033094H, NG2831538H, NG3738739H
  • FDA recall number: Z-2980-2026

The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.

Official notice

The notice's own wording from FDA.

Product
MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW | MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782; | MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;
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.
Classification
Class II (Ongoing)
Distribution
International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.
Quantity
257; 7; 16

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