Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump

Recalling company

Medtronic MiniMed, Inc.

Product

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.

Reason

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.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

Nov 2, 2025

Reported

Feb 11, 2026

Distribution

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.

Status

Ongoing

Quantity

577 units

Lot / codes

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

Company location

Northridge, CA

Recall type

Voluntary: Firm initiated

Recall number

Z-1238-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-1238-2026 in the FDA Enforcement Report. Also see FDA recall press releases.