MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Medtronic MiniMed, Inc.
The hazard
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. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model Model/UDI-DI: MMT-8600/00199150038978(10)1.1.0Model MMT-8601/00199150038985(10)1.1.0 Software Versions: 1.0.0Model 1.1.0UPC 00199150038978UPC 00199150038985Would you have heard about this one?
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