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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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
The pumps can unintentionally over-deliver insulin when the unit is elevated relative to the infusion site. They can under-deliver insulin when the unit is lowered relative to the site. Over-delivery risks severe hypoglycemia, altered mental status, seizures, coma or death. Under-delivery risks severe hyperglycemia, dehydration, diabetic ketoacidosis or death.
No injuries or incidents have been reported.
1. Stop using the product. 2. Consult your healthcare provider and follow the manufacturer’s recall instructions. 3. Do not attempt to repair or modify the device. 4. For refunds or replacements, contact Medtronic MiniMed Recall Support. Refund contact details will be provided in the manufacturer notice.
Phone: Unknown Website: Unknown Hours: Unknown
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