MiniMed Go MMT-8601Recalls & reported problems
Medtronic Minimed, Inc. · SW MMT-8601 MINIMED GO US ANDROID · Class 2
All models of MiniMed Go (2)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Jun 16, 2026Class IIOpen, Classified
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.
Z-2778-2026 · Root cause: Software design · Recall details · FDA record ↗
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- inpen™ MMT-105ELPKNAMedtronic Minimed, Inc. · Calculator, drug dose1 recall0 reports
- MiniMed Go MMT-8600Medtronic Minimed, Inc. · Calculator, drug dose1 recall0 reports
- inpen™ MMT-105ELBLNAMedtronic Minimed, Inc. · Calculator, drug dose1 recall0 reports
- inpen™ MMT-105NNGYNAMedtronic Minimed, Inc. · Calculator, drug dose1 recall0 reports
- InPen MMT-8061Medtronic Minimed, Inc. · Calculator, drug dose1 recall0 reports
- Glucommander NoneGlytec, LLC · Calculator, Drug Dose2 deaths9 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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