Use caution Medical device recall · FDA · Published July 13, 2026

Medtronic MiniMed 670G Insulin Pump Recall: Risk of Incorrect Insulin Delivery

Medtronic recalls MiniMed 670G insulin pumps with specific model numbers due to potential cleaning issues causing insulin delivery errors. Affected users should contact Medtronic for details.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2981-2026Medical device Medtr: MiniMed ›

Use caution until it’s fixed

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.

✎ GovInfoNow plain-language explainer

Medtronic is recalling MiniMed 670G insulin pumps with model numbers MMT-1781 and MMT-1782. These pumps may have been cleaned with products that could cause incorrect insulin delivery, leading to dangerous blood sugar levels. Read more at govinfonow.com/recall/697892-medtronic-minimed-670g-insulin-pump-recall-risk-of-incorrect-insulin.

Source Summary by GovInfoNow · govinfonow.com/recall/697892-medtronic-minimed-670g-insulin-pump-recall-risk-of-incorrect-insulin · Updated September 14, 2026 · FDA enforcement record: FDA #Z-2981-2026

Cite this page

“Medtronic MiniMed 670G Insulin Pump Recall: Risk of Incorrect Insulin Delivery.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/697892-medtronic-minimed-670g-insulin-pump-recall-risk-of-incorrect-insulin. Based on FDA recall #Z-2981-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2981-2026%22&limit=1).

The FDA announced on July 13, 2026, that Medtronic MiniMed is recalling seven loaner MiniMed 670G insulin pumps due to potential damage from incompatible cleaning products. The agency said the hazard could result in insulin over- or under-delivery.

How to tell if you have it

Brand: Medtronic MiniMed
Product: MiniMed 670G Insulin Pump
Model: MMT-1781, MMT-1782
Serial Numbers (MMT-1781): NG2665223H, NG2748200H, NG2748664H, NG2755237H, NG2716176H, NG3547582H
Serial Number (MMT-1782): NG2768190H
Distribution: Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland

The hazard

According to the FDA, loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad. This damage could allow moisture ingress and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.

Context

GovInfoNow's records show Medtronic MiniMed has had 13 other recalls since November 15, 2023. Recent brand recalls include a June 16, 2026 issue with the MiniMed Go App Version 1.0.0/1.1.0 and a May 27, 2026 software error in the MiniMed 780G Insulin Pump. Other recent recalls of similar products include an Insulet Omnipod DASH Pod recall on May 20, 2026, an ICU Medical Plum Duo IV Pump recall on April 29, 2026, and an Insulet Omnipod 5 Pods recall on May 20, 2026.

How to tell if you have this one

Check your pump's model number on the device or label. The affected models are MMT-1781 and MMT-1782 with specific serial numbers listed in the recall notice.

Brand
Medtr: MiniMed
Category
Medical device

FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.

Recall number	Product, codes & lots	Quantity
Z-2980-2026	MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;; 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	16
Z-2981-2026	MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;; Model/UDI-DI Serial Numbers: MMT-1781/00763000404536/NG2665223H, NG2748200H, NG2748664H, NG2755237H, NG2716176H, NG3547582H. MMT-1782/00763000404543/NG2768190H	7
Z-2982-2026	MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW; 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	257

Based on the official FDA remedy

What to do — step by step

Check Pump Model
Look for the model number on your pump's device or label to confirm if it's MMT-1781 or MMT-1782.
Contact Medtronic
Reach out to Medtronic directly for guidance on next steps and potential remedies.

How this recall unfolded

Recall timeline

FDA published this recall 44 days after the firm started it.

Jul 13, 2026Firm started the recall
Aug 18, 2026FDA classified it Class II
Aug 26, 2026Published in FDA’s Enforcement Report
Sep 8, 2026Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

Similar recalls

Other Medtr: MiniMed recalls

Latest medical device recalls

Keep exploring

More Medtr: MiniMed recalls

Link to this recall

<a href="https://govinfonow.com/recall/697892-medtronic-minimed-670g-insulin-pump-recall-risk-of-incorrect-insulin">Medtronic MiniMed 670G Insulin Pump Recall: Risk of Incorrect Insulin Delivery (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2981-2026 (July 13, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2981-2026 to see it in context.
Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.