FDAClass II · Medical device · Recalled July 15, 2026

MiniMed 780G Insulin Pump recall — Medtronic MiniMed, Inc.

Hazard: 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).

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2698-2026
Brand: Medtronic MiniMed
Classification: Class II
Units affected: 778
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Description

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

Affected products

MiniMed 780G Insulin Pump

Companies & origin

Recalling firm location: Northridge, CA, United States
Firm address: 18000 Devonshire St, N/A, 91325-1219

Identifying details (verbatim from the notice)

Product codes / lots: UDI-DI/GTIN: A7630006392701, 00763000521554, 00763000639273, A7630006392301, 00199150035687, A7630007325603, A7630007325601, 00763000639235, A7630007325604, 00763000384289, 00763000521530, A7630007325401, 00763000521547, A7630006392601, A7630006392201, 00763000639228, 00199150035663, 00763000639266, A7630007325404, 00199150035694, 00763000442194, A7630007325403, 00763000521523. Software version 6.62
Distribution: International distribution to the countries of Spain, Great Britain, Netherlands, Italy.
Firm notified the public via: N/A
FDA event ID: 99207
Recall initiated: May 27, 2026
FDA classified: July 8, 2026
FDA report date: July 15, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 24, 2026 at 12:00 AM UTC.

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