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device recall
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Medtronic MiniMed, Inc. device recall (Cls II)

February 13, 2026updated 5mo ago
community read0 votes

MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851) — Reason: 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. — Status: Ongoing

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same company · ±60 days · 6

  • device recallMedtronic MiniMed, Inc. device recall (Cls II)Feb 13, 2026
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  • device recallMedtronic MiniMed, Inc. device recall (Cls II)Feb 13, 2026
  • device recallMedtronic MiniMed, Inc. device recall (Cls II)Feb 13, 2026

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