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Medtronic MiniMed, Inc. recalls MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Recalled July 29, 2026 · FDA recall Z-2778-2026 · Medtronic MiniMed
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. · FDA Class II
Units
3,465
Sold at
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.
Description
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.
Product
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Manufacturer(s)
Medtronic MiniMed, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →