Medtronic MiniMed recalls Go app versions 1.0.0 and 1.1.0 for iOS and Android devices. These versions may not trigger nighttime alerts when certain settings are disabled, risking missed insulin doses and hyperglycemia.
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated alerts will not be triggered during the nighttime. This could result in missed rapid-acting insulin doses without the user s knowledge, and may lead to delayed therapy and an increased risk of hyperglycemia.
Medtronic MiniMed is recalling its Go app versions 1.0.0 and 1.1.0 for iOS and Android devices. If nighttime alerts are turned off while missed dose or high glucose alerts are enabled, the app won't trigger nighttime alerts, which could lead to missed insulin doses and hyperglycemia.
When the 'Set day and night' feature is turned off and missed dose or high glucose alerts are enabled, the app stops sending nighttime alerts. This means users might miss insulin doses during the night without realizing it, increasing the risk of high blood sugar levels.
People using Medtronic MiniMed Go app versions 1.0.0 or 1.1.0 on iOS (MMT-8600) or Android (MMT-8601) devices are affected. Those with diabetes who rely on the app for nighttime alerts are most at risk.
Check your MiniMed Go app version by going to Settings > About. Affected versions are 1.0.0 and 1.1.0 for iOS (MMT-8600) and Android (MMT-8601) devices.
Go to Settings > About in the MiniMed Go app to see the version number.
Update to the latest version of the MiniMed Go app to fix the alert issue.
App versions 1.0.0 and 1.1.0 for iOS (MMT-8600) and Android (MMT-8601) devices.
The app may not trigger nighttime alerts when the 'Set day and night' feature is turned off and missed dose or high glucose alerts are enabled, which could lead to missed insulin doses and hyperglycemia.
No, but you should update to the latest version to fix the issue. The recall does not require immediate discontinuation.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-2778-2026 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-2778-2026 from Medtronic MiniMed. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
