Official recall record
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 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.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-09-16.
Record last checked against the registry on 2026-09-16.
Other recalls from this brand
- 2026-07-13 · US FDA — Medical Devices
MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782; - 2026-07-13 · US FDA — Medical Devices
MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712; - 2026-07-13 · US FDA — Medical Devices
MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.