# FDA recall Z-2778-2026

> **Medtronic MiniMed, Inc.** · Class II · device recall initiated 2026-06-16.

## 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.

## 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.

## Key facts

- **Recall number:** Z-2778-2026
- **Recalling firm:** Medtronic MiniMed, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-16
- **Report date:** 2026-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northridge, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2778-2026

## Citation

> AI Analytics. FDA recall Z-2778-2026. Retrieved 2026-09-03 from https://api.ai-analytics.org/recall/Z-2778-2026. Source: US FDA. Licensed CC0.

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