Reported Apr 1, 2026 · Ongoing

MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61

Medtronic MiniMed, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medtronic MiniMed, Inc. · 18000 Devonshire St · Northridge, CA · 91325-1219

Is this the product you have?

  • MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61
Lot codes and dates
  • MiniMed 780G Model NumberMMT-1884
  • UDI-DI code763000414344
  • Serial Numbers

    554 of 554 codes

    • NG2445689H
    • NG2445778H
    • NG2455039H
    • NG2461527H
    • NG2461608H
    • NG2471389H
    • NG2471573H
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    • NG2576778H
    • NG2579113H
    • NG2579956H
    • NG2580323H
  • NG3076597H NG3078872H UDI-DI code763000439859
  • Serial Numbers
    • NG2521143H
    • NG2583395H
    • NG2617162H
    • NG2629426H
    • NG2629644H
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    • NG2630635H
    • NG2640853H
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    • NG2724308H
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    • NG2961005H
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    • NG2981500H
    • NG2981639H
    • NG3001480H
    • NG3039155H
    • NG3039437H
    • NG3039662H
    • NG3039860H
    • NG3051945H
    • NG3052291H
    • NG3052464H
    • NG3056782H
    • NG3065697H
    • NG3075841H
    • NG3076011H
    • NG3076138H
    • NG3078541H
    • NG3078685H
    • NG3078710H
  • NG3078719H NG3078922H UDI-DI code763000545604
  • Serial Numbers

    1,303 of 1,303 codes

    • NG3104959H
    • NG3105146H
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    • NG3105212H
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    • NG3105487H
    • NG3105501H
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    • NG3105755H
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    • NG3106131H
    • NG3106145H
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    • NG3106258H
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    • NG3106396H
    • NG3106549H
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    • NG3106695H
    • NG3106726H
    • NG3106755H
    • NG3106763H
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    • NG3106808H
    • NG3106873H
    • NG3106884H
    • NG3106891H
    • NG3110328H
    • NG3110411H
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    • NG3110782H
    • NG3110804H
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    • NG3110867H
  • NG3569799H NG3570451H UDI-DI code763000640095
  • Serial Numbers

    100 of 100 codes

    • NG3104580H
    • NG3104789H
    • NG3110101H
    • NG3116173H
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    • NG3163071H
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    • NG3184720H
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    • NG3194657H
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  • NG3441974H NG3442442H UDI-DI code763000758547
  • Serial Numbers

    927 of 927 codes

    • NG3454210H
    • NG3454243H
    • NG3454278H
    • NG3454293H
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    • NG3454383H
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    • NG3454878H
    • NG3455790H
    • NG3455818H
    • NG3455830H
    • NG3455832H
    • NG3455838H
    • NG3455845H
    • NG3455851H
    • NG3455857H
    • NG3455884H
    • NG3455950H
    • NG3455951H
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    • NG3455992H
    • NG3455994H
    • NG3456393H
    • NG3456399H
    • NG3456400H
    • NG3456426H
    • NG3456455H
    • NG3456470H
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    • NG3456520H
    • NG3456628H
    • NG3456669H
    • NG3456684H
    • NG3456703H
    • NG3456714H
    • NG3456721H
    • NG3456769H
    • NG3456847H
    • NG3456889H
    • NG3456894H
    • NG3456930H
    • NG3457031H
    • NG3457075H
Amount recalled
26,851 pumps

Where it was sold

Why it was recalled

Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61, and 6.62), which could result in a risk of hypoglycemia or hyperglycemia due to inaccuracies in insulin delivery (either under-delivery, over-delivery, or cessation of delivery).

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 3:31 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.