Reported Jul 29, 2026 · Ongoing · Updated Sep 16, 2026
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Medtronic MiniMed, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic MiniMed, Inc. · 18000 Devonshire St · Northridge, CA · 91325-1219
Is this the product you have?
- MiniMed Go App
- Model
MMT-8600 (iOS)MMT-8601 (Android)
- Lot codes and dates
- Model/UDI-DI
MMT-8600/00199150038978(10)1.1.0MMT-8601/00199150038985(10)1.1.0
- Software Versions
1.0.01.1.0
- Model/UDI-DI
- Amount recalled
- 3,465
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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