MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With… — Class II medical device recall Z-1238-2026
Ongoing recall by Medtronic MiniMed, Inc., reported 2026-02-11, distributed in AL, AR, AZ, CA, CO, CT, DE, FL…. A software timing and processor communication issue in MiniMed" 780G software version 6.60 may trigger Pump Er
| Recall number | Z-1238-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic MiniMed, Inc., Northridge, CA, United States |
| Recall initiated | 2025-11-02 |
| Classified | 2026-02-02 |
| Reported by FDA | 2026-02-11 |
| Distributed | 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, WV |
| Countries outside the US | IL |
| Quantity | 577 units |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 00199150003686, 00763000414344, 00763000545604, 00763000578640, 00763000586195, 00763000640095, 00763000758547, 00763000819378, 00763000819385, 00763000819392, 00763000865665, 00763000924089, 00763000924102, 00763000924119 |
| Serial numbers | 503, NG2473989H, NG2752574H, NG2774486H, NG2811465H, NG2922632H, NG2961968H, NG2983018H, NG3050369H, NG3051461H, NG3106884H, NG3110782H, NG3114301H, NG3116129H, NG3147620H, NG3163771H, NG3165546H, NG3183875H, NG3184692H, NG3226459H, NG3243700H, NG3245352H, NG3246406H, NG3253416H, NG3271492H and 475 more |
| Model numbers | MMT-1884, MMT-1886 |
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1238-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.