Medtronic MiniMed recalled 95,704 MiniMed 770G insulin pumps worldwide after finding insulin delivery can misbehave when the pump height changes. Over-delivery can cause severe hypoglycemia and death; under-delivery can cause hyperglycemia and death. Stop using the device and follow the manufacturer’s recall instructions immediately.
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medtronic MiniMed, Inc. or your healthcare provider for instructions. Notification method: Letter
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This insulin pump delivers continuous subcutaneous insulin to people with diabetes. The MiniMed 770G and related pumps are used to automate insulin delivery.
The device’s height relative to the infusion site can alter insulin flow due to hydrostatic and hydrodynamic pressure changes. Over-delivery risks hypoglycemia and death; under-delivery risks hyperglycemia, dehydration, DKA, and death.
This recall is not stated as part of a broader industry pattern.
Consumers could face life-threatening diabetes complications if the device mis-delivers insulin. The recall involves a large, global population of users.
Look on the device label, user guide, and original packaging for model numbers and UDI. Manufacturer recall notices will detail next steps.
Refund or replacement processing will follow manufacturer instructions; typical recall timelines range from several weeks to a few months.
Keep the recall notice, your pump’s model and serial numbers, purchase receipts, and all communications with the manufacturer and healthcare providers.
Product: MiniMed 770G Insulin Pump Brand: Medtronic MiniMed Models: MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892 Distribution: Worldwide, including US states and international markets Original recall date: 2026-02-13 Recall number: Z-1742-2026 Quantity: 95,704 units Associated series: Paradigm, 600 series, BLE 700 series URL: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-1742-2026 Price: Unknown Sold since: Unknown
No injuries or incidents have been reported.
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