MiniMed 780G Insulin Pump — Class II medical device recall Z-2698-2026
Ongoing recall by Medtronic MiniMed, Inc., reported 2026-07-15. A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, th
| Recall number | Z-2698-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic MiniMed, Inc., Northridge, CA, United States |
| Recall initiated | 2026-05-27 |
| Classified | 2026-07-08 |
| Reported by FDA | 2026-07-15 |
| Countries outside the US | ES, GB, IT, NL |
| Quantity | 778 |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 00199150035663, 00199150035687, 00199150035694, 00763000384289, 00763000442194, 00763000521523, 00763000521530, 00763000521547, 00763000521554, 00763000639228, 00763000639235, 00763000639266, 00763000639273, 07630007325603 |
| Model numbers | MMT-1885, MMT-1886, MMT-1895, MMT-1896 |
Product
MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
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).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2698-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.