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Open, Classified

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

FDA Recall Z-2698-2026 · Posted 2026-07-08

Recalling FirmMedtronic MiniMed, Inc.
Recall StatusOpen, Classified
Product CodeQFG
Date Initiated2026-05-27
Product Quantity778

Reason for Recall

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).

Firm Action

On 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

Root Cause

Software design

Distribution Pattern

International distribution to the countries of Spain, Great Britain, Netherlands, Italy.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K251032MiniMed 780G insulin pumpMedtronic Minimed, Inc. · 2025-07-01

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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