# FDA device recall: MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)

> recall · VERIFIED · 2026-06-16

Firm: Medtronic MiniMed, Inc. · Class II · 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 durin

- Company: Medtronic MiniMed, Inc.
- Sector: digital health
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.