Official recall record
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-06-16
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00199150038978
- Brand on record
- Medtronic MiniMed, Inc.
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-09-16.
Same barcode in other registries
The same EAN appears in 1 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2026-09-02 · US FDA — Medical Devices
Generic Name: MiniMed Go App Generic Name: MiniMed Go App Model/Catalog Number: MMT-8600 (iOS), MMT-8601 (Android) So
Other recalls from this brand
- 2026-09-11 · US FDA — Medical Devices
CareLink Clinic, REF: MMT-7350 - 2026-09-02 · US FDA — Medical Devices
Generic Name: MiniMed Go App Generic Name: MiniMed Go App Model/Catalog Number: MMT-8600 (iOS), MMT-8601 (An - 2026-08-20 · US FDA — Medical Devices
Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Pro
All 32 official recall notices naming Medtronic MiniMed, Inc. on this site →