ClearanceBrief
Recall Z-2698-2026 ยท QFG Alternate Controller Enabled Insulin Infusion Pump

Medtronic MiniMed, Inc.

MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896

DateJul 8, 2026 (initiated May 27, 2026)
StatusOpen, Classified
ReasonA 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).
Root causeSoftware design
ActionOn 5/27/2026, field safety notices were emailed to customers who were asked to do the following: 1) Update insulin pump software to version 6.63. The update may take up to 3 hours to complete. 2) Reply to this email to confirm that you have read and understood this notification and, where applicable, completed the required action. If you have questions, contact the firm at 01923 205167
Quantity778
DistributionInternational distribution to the countries of Spain, Great Britain, Netherlands, Italy.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K251032MiniMed 780G insulin pump
Medtronic Minimed, Inc., Jul 1, 2025