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Health & beauty United States Recall (ongoing)

Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump

MiniMed 780G Insulin Pump (REF MMT-1885, MMT-1886, MMT-1895, MMT-1896; software version 6.62) is affected. Medtronic recalled the pumps because a software anomaly when paired with the Instinct sensor can cause the pump to unexpectedly stop delivering insulin and display Pump Error 53 immediately followed by Pump Error 23, which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA).

What's being recalled

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

Recalling firm: Medtronic MiniMed, Inc., Northridge, CA, United States.

How to identify it

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

The 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).

What to do

Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.

The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.

Where it was sold

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

The official notice

This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.

Read the official notice (opens in a new tab)

A little guidance

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