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.
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Contact the company
📍Recalling firmMedtronic MiniMed, Inc.18000 Devonshire St · Northridge, CA 91325-1219
✎ GovInfoNow plain-language explainer
Medtronic MiniMed is recalling the MiniMed 780G insulin pump because a software timing issue can cause Pump Error 43 or Pump Error 41, which stops insulin from being delivered. This affects pumps with catalog numbers MMT-1884 and MMT-1886 that have software version 6.60 installed. The recall covers 577 units distributed in the U.S. and Israel. Read more at govinfonow.com/recall/50828-medtronic-minimed-780g-insulin-pump-software-version-6-60-recall.
“Medtronic MiniMed 780G Recall: Software Error Stops Insulin Delivery.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/50828-medtronic-minimed-780g-insulin-pump-software-version-6-60-recall. Based on FDA recall #Z-1238-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1238-2026%22&limit=1).
The FDA announced on Nov. 2, 2025, that Medtronic MiniMed, Inc. is recalling MiniMed 780G insulin pumps due to a software issue that may suspend insulin delivery. Owners should contact the company for a remedy.
How to tell if you have it
Brand: Medtronic
Product: MiniMed 780G Insulin Pump
Catalog Numbers: MMT-1884, MMT-1886
Software Version: 6.60
Units affected: 577
The hazard
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.
Context
GovInfoNow's records show Medtronic MiniMed, Inc. has 13 other recalls on record since 2023-11-15. Other recent recalls of similar products include Medtronic MiniMed 780G Insulin Pump Recall: Software Error Causes Insulin Stoppage (2026-05-27), Medtronic MiniMed Go App Version 1.0.0/1.1.0 May Cause Missed Insulin Doses (2026-06-16), and Medtronic MiniMed 670G Insulin Pump Recall: Risk of Incorrect Insulin Delivery (2026-07-13). FDA's MAUDE device-report database contains 108,633 reports in FDA's MAUDE database naming MiniMed 780G (product code OZP), received since November 2024, 18,425 of them marked serious and 94 listing a death.
How to tell if you have this one
Check if your device is a MiniMed 780G Insulin Pump with catalog number MMT-1884 or MMT-1886 and software version 6.60. You can verify the specific serial numbers affected by visiting the official recall notice, as there are hundreds of unique serial numbers listed for both U.S. and Israel distributions.
Brand
Medtronic MiniMed
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Your Device Details
Verify if your MiniMed 780G pump has catalog number MMT-1884 or MMT-1886 with software version 6.60.
Contact Medtronic for Remedy
The recall record does not specify the current remedy steps; contact Medtronic MiniMed directly for instructions on how to proceed with your specific unit.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 45 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA 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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-1238-2026 (November 2, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1238-2026 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 13, 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.