Recall
FDAHealthJune 16, 2026

Medtronic MiniMed, Inc. — MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
June 16, 2026

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.

What's affected?

Product
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Lot code
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

Additional details

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

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 3,465.

View original FDA notice →

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