{"url_path":"/fda/device/recalls/Z-2778-2026","section_key":"summary","section_title":"DEVICE Recall: Medtronic MiniMed, Inc. — MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-06-16","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2778-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Medtronic MiniMed, Inc."},"word_count":173,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2778-2026\n\n**Recalling firm:** Medtronic MiniMed, Inc.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-06-16\n**Report date:** 2026-07-29\n\n## Product\nMiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)\n\n## Reason\nFor 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.\n\n## Affected lots\nModel/UDI-DI: MMT-8600/00199150038978(10)1.1.0, MMT-8601/00199150038985(10)1.1.0  Software Versions: 1.0.0, 1.1.0\n\n## Distribution\nWorldwide - 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."}