Official recall record

Generic Name: MiniMed Go App Generic Name: MiniMed Go App Model/Catalog Number: MMT-8600 (iOS), MMT-8601 (Android) Software Version: Soft

US FDA — Medical Devices · 2026-09-02 · United StatesClass II

Issuing authority: US FDA — Medical Devices
Recall initiated by firm: 2026-09-02
Country of alert: United States
Alert level: Class II
Alert type: recall
Barcode (EAN/GTIN): 00199150038978
Brand on record: Medtronic MiniMed, Inc.

What the authority reported

A software defect in which existing users who had previously configured and enabled the long-acting dose reminder feature in version 1.2.0 or earlier experienced failure of the long-acting dose reminder after updating their app to version 1.2.1. The long-acting dose reminder is an optional feature that, when enabled, triggers a notification at the scheduled time to remind users to take their long-acting insulin dose. The issue was caused by a type cast exception during database migration that occurs upon app update to version 1.2.1 causing a silent failure that prevented the creation of new alerts. Failure to receive the long-acting dose reminder may result in missed or delayed insulin doses, potentially leading to hyperglycemia. Conversely, if users are uncertain whether they took their dose due to the missing reminder, inadvertent duplicate dosing may occur, potentially resulting in hypoglycemia.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-11-13.

More recalls: US FDA — Medical Devices · United States · all filters

Same barcode in other registries

The same EAN appears in 1 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.

2026-06-16 · US FDA — Medical Devices
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)

Other recalls from this brand

2026-09-11 · US FDA — Medical Devices
CareLink Clinic, REF: MMT-7350
2026-08-20 · US FDA — Medical Devices
Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Pro
2026-07-13 · US FDA — Medical Devices
MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;

All 32 official recall notices naming Medtronic MiniMed, Inc. on this site →

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