Medtronic MiniMed, Inc. is recalling approximately 26,851 MiniMed 780G insulin pumps, models MMT-1884 and MMT-1886, with software versions 6.60, 6.61, and 6.62. The recall was initiated because three specific software defects—Pump Error 53, BG check errors, and Critical Pump Errors—can cause the device to deliver the wrong amount of insulin or stop delivery entirely. These pumps were distributed nationwide and in Israel between January 2026 and the current recall date. Consumers should immediately contact their healthcare provider for guidance on managing their diabetes if their pump displays these specific error codes.
The software defects can lead to the under-delivery or over-delivery of insulin, or a complete cessation of insulin delivery without adequate warning. This poses a significant risk of hypoglycemia (dangerously low blood sugar) or hyperglycemia (dangerously high blood sugar), both of which can lead to serious medical complications or death.
healthcare provider or manufacturer consultation.
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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