MiniMed 780G Insulin Pump
Medical device recall Z-1238-2026. Published in FDA’s Enforcement Report on Feb 11, 2026.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Feb 11, 2026. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- 45 states named in where it went
- 577 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
A software timing and processor communication issue in MiniMed” 780G software version 6.60 may trigger Pump Error 43 and/or Pump Error 41, resulting in suspension of insulin delivery.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump is indicated for use by patients age 7-80 years with Type 1 diabetes, whose total daily dose of insulin is 8 units per day or more. The MiniMed 780G system is intended for continuous delivery of basal insulin at selectable rates, and the administration of insulin boluses at selectable amounts for the management of type 1 diabetes mellitus in persons seven years of age and older requiring insulin. The system is also intended to continuously monitor glucose values in the fluid under the skin. The MiniMed 780G system includes SmartGuard technology, which can be programmed to automatically adjust insulin delivery based on continuous glucose monitoring (CGM) sensor glucose values and can suspend delivery of insulin when the SG value falls below or is predicted to fall below predefined threshold values.
577 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
MiniMed 780G MMT-1884 (US) UDI-DI codes: 00199150003686 00763000414344 00763000545604 00763000578640 00763000586195 00763000640095 00763000758547 00763000819378 00763000819385 00763000819392 00763000865665 00763000924089 00763000924102…
Every code shown here, 1,996 characters
MiniMed 780G MMT-1884 (US) UDI-DI codes: 00199150003686 00763000414344 00763000545604 00763000578640 00763000586195 00763000640095 00763000758547 00763000819378 00763000819385 00763000819392 00763000865665 00763000924089 00763000924102 00763000924119 76300075854701 76300081937801 76300081938501 76300096001801 76300096003201 76300096004901 Serial Numbers: NG3666779H NG3811803H NG3926926H NG3944480H NG4116699H NG4173817H NG3334724H NG3750453H NG3874105H NG3924178H NG3926632H NG3927673H NG3944520H NG4023801H NG4029254H NG4097850H NG4146571H NG4170515H NG4200310H NG4177489H NG4178626H NG2752574H NG3423286H NG3838934H NG3926282H NG3948645H NG4017463H NG4010052H NG4174745H NG4178395H NG3502087H NG3634564H NG3756694H NG3871741H NG3919620H NG3927825H NG4164005H NG3729206H NG3839883H NG3884748H NG3908444H NG3961353H NG4068853H NG4179772H NG3106884H NG3116129H NG3271492H NG3351525H NG3458389H NG3464645H NG3490545H NG3482017H NG3520991H NG3593959H NG3515336H NG3467707H NG3563980H NG3654085H NG3653614H NG3662418H NG3631555H NG3686291H NG3685575H NG3721941H NG3722374H NG3751345H NG3762687H NG3773707H NG3804837H NG3785876H NG3815941H NG3809816H NG3809672H NG3809900H NG3811760H NG3857851H NG3848444H NG3865466H NG3871979H NG3923251H NG3928992H NG3946093H NG3944898H NG3945847H NG3966122H NG3925413H NG3984252H NG4071539H NG3891538H NG4099361H NG4097100H NG3966344H NG4115711H NG4170457H NG4170650H NG4171411H NG4179308H NG4165581H NG4166028H NG4174665H NG4176618H NG4197135H NG4198605H NG4194835H NG4213027H NG2811465H NG2922632H NG3050369H NG2473989H NG3110782H NG3165546H NG3245352H NG3491506H NG3504053H NG3503998H NG3467406H NG3727425H NG3718393H NG3741705H NG3740402H NG3754549H NG3743216H NG3838750H NG3859322H NG3846048H NG3851889H NG3869122H NG3878439H NG3920428H NG3941436H NG3919322H NG3927745H NG3946295H NG3923212H NG3941150H NG3978427H NG3945129H NG3952217H NG4041650H NG4019446H NG4010956H NG4025469H NG4079778H NG4089972H NG4087937H NG4082944H NG4068836H NG4075347H NG4078121H…
FDA’s list runs to 6,782 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide - U.S. National distribution including in the states of AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV. The country of Israel.
The states and territories these words name
45 states and territories.
Every one of them
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
The words say it went outside the United States too.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Nov 2, 2025.
- FDA classified it on Feb 2, 2026.
- FDA’s Enforcement Report published it on Feb 11, 2026.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Medtronic MiniMed, Inc., of Northridge, CA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 6,782 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.