FDA · Class II · August 26, 2026

Medtronic MiniMed recall: MiniMed

Medtronic MiniMed, Inc. is recalling MiniMed – 16; 7; 257. The U.S. Food and Drug Administration published the recall on August 26, 2026; it began on July 13, 2026. Distributed International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland..

Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.

Illustration: An FDA laboratory that tests medical devices – not the recalled product. Photo: U.S. Food and Drug Administration, public domain.

Product	MiniMed
Brand	Medtronic MiniMed
Company	Medtronic MiniMed, Inc.
Type	Medical devices
Classification	Class II
Recall date	July 13, 2026
Published by FDA	August 26, 2026
Quantity	16; 7; 257
Recall ID	99374

As listed by FDA

Recalled products (3)

MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;
FDA recall number
Z-2980-2026
Codes, lots and dates
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
Quantity
16
Classification
Class II
MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
FDA recall number
Z-2981-2026
Codes, lots and dates
Model/UDI-DI Serial Numbers: MMT-1781/00763000404536/NG2665223H, NG2748200H, NG2748664H, NG2755237H, NG2716176H, NG3547582H. MMT-1782/00763000404543/NG2768190H
Quantity
7
Classification
Class II
MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW
FDA recall number
Z-2982-2026
Codes, lots and dates
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, NG3153405H, NG3153788H, NG3153908H, NG3154527H, NG3151598H, NG2854971H, NG3155196H, NG3155202H, NG3155341H, NG3091491H, NG3155557H, NG3081498H NG3155688H, NG3155020H, NG3508565H, NG3155419H, NG3507536H, NG3091563H, NG3082036H, NG3154689H, NG3154995H, NG3508504H, NG3514345H, NG3509850H, NG3527505H, NG3514547H, NG3527469H, NG3504333H, NG3504598H, NG3505071H, NG3505220H, NG3505273H, NG3514617H, NG3506727H, NG3085044H, NG3507542H, NG3507547H, NG3514448H, NG3508303H, NG3508350H, NG3508371H, NG3514612H, NG3508511H, NG3508617H, NG3508698H, NG3508707H, NG3508757H, NG3508799H, NG3508903H, NG3509138H, NG3509295H, NG3509299H, NG3509452H, NG3509685H, NG3509689H, NG3509836H, NG3509914H, NG3509925H, NG3514375H, NG3514441H, NG3505246H, NG3505166H, NG3505283H, NG3151570H, NG3154948H, NG3514667H, NG3527165H, NG3527243H, NG3527298H, NG3527468H, NG3527480H, NG3527491H, NG3527580H, NG3527529H, NG3527543H, NG3527571H, NG3527574H, NG3092722H, NG3527581H, NG3527611H, NG3527637H, NG3527642H, NG3527672H, NG3527710H, NG3527737H, NG3527760H, NG3527865H, NG3527918H, NG3527961H, NG3527989H, NG3528017H, NG3528023H, NG3528036H, NG3528061H, NG3528120H, NG3528147H, NG3528156H, NG3528158H, NG3528180H, NG3528218H, NG3528226H, NG3528378H, NG3539964H, NG3539969H, NG3539970H, NG3539999H, NG3540001H, NG3540013H, NG3540029H, NG3540046H, NG3540053H, NG3540084H, NG3540191H, NG3540270H, NG3540310H, NG3540320H, NG3540581H, NG3540604H, NG3540628H, NG3540629H MMT-1886CLW/00763000442194, 00763000974381/NG2966956H, NG2970938H, NG2986362H, NG3013390H, NG3057910H, NG3167493H, NG3466128H, NG3098147H, NG3136398H, NG3137113H, NG3139432H, NG3143920H, NG3144721H, NG3145486H, NG3145488H, NG3471528H, NG3167609H, NG3147120H, NG3147035H, NG3430059H, NG3438451H, NG3464758H, NG3163796H, NG3166778H, NG3409587H, NG3167450H, NG3167623H, NG3167967H, NG3169694H, NG3170253H, NG3321081H, NG3409583H, NG3409611H, NG3409656H, NG3409680H, NG3409697H, NG3409716H, NG3409807H, NG3409825H, NG3409831H, NG3409854H, NG3409925H, NG3409959H, NG3410005H, NG3410053H, NG3410092H, NG3410111H, NG3410166H, NG3410189H, NG3410227H, NG3410233H, NG3410243H, NG3410279H, NG3410304H, NG3410389H, NG3410398H, NG3429103H, NG3429377H, NG3429485H, NG3429881H, NG3430107H, NG3430448H, NG3437945H, NG3437957H, NG3438394H, NG3470788H, NG3466185H, NG3466619H, NG3466620H, NG3467368H, NG3467586H, NG3468759H, NG3469430H, NG3469907H, NG3470728H, NG3168104H, NG3472157H, NG3169669H, NG3170079H, NG3430111H, NG3429099H, NG3437621H, NG3167969H, NG3465813H, NG3167397H
Quantity
257
Classification
Class II

Exactly as the agency lists them

Identifiers and details

FDA event ID: 99374
Initiated: Voluntary: Firm initiated
Status: Ongoing
Firm location: Northridge, CA, United States

Why it was recalled

The reason the FDA lists: “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.”

Where it was sold

Distribution as the FDA records it: “International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.”

What to do

Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.

Official notice: FDA Enforcement Report record (event 99374, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.

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FAQ

About this recall

Is Medtronic MiniMed MiniMed recalled?

Yes. Medtronic MiniMed, Inc. recalled it on July 13, 2026; FDA published it August 26, 2026 (Class II). Only the lots, dates or models listed on this page are included.

Why was it recalled?

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 should I do if I have it?

Where was it sold?

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

Recalls

More recalls

Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.