Reported Jul 15, 2026 · Ongoing
MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
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 Insulin Pump
- REF
MMT-1885MMT-1886MMT-1895MMT-1896
- Lot codes and dates
- UDI-DI/GTIN
A76300063927010076300052155400763000639273A763000639230100199150035687A7630007325603A763000732560100763000639235A76300073256040076300038428900763000521530A763000732540100763000521547A7630006392601A7630006392201007630006392280019915003566300763000639266A76300073254040019915003569400763000442194A763000732540300763000521523. Software version 6.62
- UDI-DI/GTIN
- Amount recalled
- 778
Why it was recalled
A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA).
This product could cause temporary or reversible health problems — stop using it.
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