Compare the complete identifiers. Name similarity alone is not a confirmed match.
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
| Product or model | Codes and lots | Quantity | Recall number |
|---|---|---|---|
| MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android) | 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 | 3,465 | Z-2778-2026 |
The agency's statement is shown without a site-authored severity score.
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.
Agency classification: Class II
Only instructions associated with this recall event qualify as an action.
Consumer action is not available in the associated official record. The site does not infer or generate a replacement.
The linked agency record controls if any information differs.
Official scope
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.
Distribution is context, not a confirmed item match. Compare the model, lot, UPC, NDC, or serial number above.
No material affected-item, risk, action, or status change has been recorded since this page entered the tracker.
