⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a
very recent recall may be missing. Everything shown is accurate as of the last checked time on this page —
for anything time-critical, confirm with the official sources linked below.
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
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 23, 2026 at 11:04 PM UTC.
Report a data error on this page