Medtronic MiniMed recalled 13,811 MiniMed 700G insulin pumps sold worldwide through multiple retailers. The pumps can deliver too much or too little insulin when the pump height relative to the infusion site changes due to gravity. Consumers should stop using the device and follow recall instructions in the letter notice sent to affected users.
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 700G Insulin Pump. Models: MMT-1801, MMT-1805, MMT-1850, MMT-1851. Sold worldwide, including all US states listed in recall distribution. Recall date: 2026-02-13. Report date: 2026-04-08. Quantity recalled: 13,811 units. Manufacturer: Medtronic MiniMed, Inc. Country of origin: Unknown. Price: Unknown.
A design flaw causes unintended insulin delivery when the pump is elevated or lowered relative to the infusion site. Over-delivery can lead to severe hypoglycemia, altered mental status, seizures, coma or death. Under-delivery can cause severe hyperglycemia, dehydration, diabetic ketoacidosis or death.
No injuries or incidents have been reported.
1. Stop using the product. 2. Follow recall instructions provided by the manufacturer. 3. Contact Medtronic MiniMed or your healthcare provider for instructions. 4. Monitor for symptoms of hypo- or hyperglycemia and seek medical advice if needed. 5. For refunds or replacements, follow the recall notice instructions and contact Medtronic MiniMed for remedy details.
Recallnotice: Letter-based notification. For instructions and refunds or replacements, visit the FDA recall page or Medtronic recall resources. FDA enforcement page: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-1744-2026
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