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FDA (Device enforcement)Recalled 2026-05-27class ii

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

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).

Details from the source

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). Distribution: International distribution to the countries of Spain, Great Britain, Netherlands, Italy. Quantity: 778 Lot/code info: 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

UPC codes

00763000521554, 00763000639273, 00199150035687, 00763000639235, 00763000384289, 00763000521530, 00763000521547, 00763000639228, 00199150035663, 00763000639266, 00199150035694, 00763000442194, 00763000521523

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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