Medtronic MiniMed recalls MiniMed Go App over alerts that may not sound at night
In MiniMed Go app versions 1.0.0 and 1.1.0, when Set day and night is turned OFF, missed dose or Correct high glucose alerts will not be triggered at night, which could mean missed rapid-acting insulin doses without the user knowing and a higher risk of hyperglycemia.
What to do
The notice does not give instructions. Read the official notice for details.
Do not stop taking a prescribed medicine, or stop using a device you rely on, until you have talked to your pharmacist or doctor.
Recall details
- Product
- MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
- Company
- Medtronic MiniMed, Inc.
- Hazard
- 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.
- Units
- 3,465
- Where sold
- Worldwide - US Nationwide distribution in the states and territories of PR, OH, WA, IL, NC, PA, VA, MN, ID, CA, UT, MI, NJ, MS, SC, CO, AZ, OR, AR, MO, TX, AL, FL, NY, IN, TN, IA, WI, MA, LA, OK, GA, KS, NM, CT, KY, NH, NV, MD and the countries of Australia, Switzerland, Germany, Denmark, Spain, Finland, Iceland, Norway, Sweden.
- FDA classification
- Class II · Ongoing
- Classified by FDA
- July 23, 2026
- Recall started
- June 16, 2026
- FDA enforcement report
- July 29, 2026
- Identifiers
- Codes: Model/UDI-DI: MMT-8600/00199150038978(10)1.1.0, MMT-8601/00199150038985(10)1.1.0 Software Versions: 1.0.0, 1.1.0
- FDA recall number: Z-2778-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- Product
- MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
- Reason for recall
- 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.
- Classification
- Class II (Ongoing)
- Distribution
- Worldwide - US Nationwide distribution in the states and territories of PR, OH, WA, IL, NC, PA, VA, MN, ID, CA, UT, MI, NJ, MS, SC, CO, AZ, OR, AR, MO, TX, AL, FL, NY, IN, TN, IA, WI, MA, LA, OK, GA, KS, NM, CT, KY, NH, NV, MD and the countries of Australia, Switzerland, Germany, Denmark, Spain, Finland, Iceland, Norway, Sweden.
- Quantity
- 3,465
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