Medtronic MiniMed, Inc. has recalled 577 MiniMed 780G insulin pumps, including models MMT-1884 (US) and MMT-1886 (Israel), because a software timing error can cause the device to stop delivering insulin. Specifically, software version 6.60 may trigger a Pump Error 41 or 43, which suspends all insulin delivery. Consumers should check their device software version and serial number to see if their pump is affected.
A communication issue between internal processors causes the pump to stop delivering insulin, which can lead to high blood sugar (hyperglycemia) or diabetic ketoacidosis (DKA) if not addressed immediately. No injuries or deaths have been reported specifically in this data summary.
Units with Software Version 6.60
Units with Software Version 6.60
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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