Every recall we track for Medtronic MiniMed, Inc. — 42 in all — plus the complaints and injury reports the public filed about them.
Medtronic recalls MiniMed 640G insulin pumps with model numbers MMT-1711 and MMT-1712 that may have been damaged by improper cleaning, risking incorrect insulin delivery and health complications.
Medtronic recalls MiniMed 670G insulin pumps with specific model numbers due to potential cleaning issues causing insulin delivery errors. Affected users should contact Medtronic for details.
Medtronic recalls MiniMed 780G insulin pumps with specific model numbers due to potential damage from incompatible cleaning products, which could cause incorrect insulin delivery and health risks.
Medtronic MiniMed recalls Go app versions 1.0.0 and 1.1.0 for iOS and Android devices. These versions may not trigger nighttime alerts when certain settings are disabled, risking missed insulin doses and hyperglycemia.
Medtronic recalls MiniMed 780G insulin pumps with specific software versions due to a software anomaly that can cause insulin delivery to stop when paired with Instinct sensors, risking hyperglycemia or diabetic ketoacidosis.
Medtronic recalls MiniMed 670G insulin pumps (MMT-1760 to MMT-1782) due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia.
Medtronic recalls MiniMed 700G insulin pumps (MMT-1801, MMT-1805, MMT-1850, MMT-1851) due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia.
Medtronic recalls MiniMed 770G insulin pumps (MMT-1880-1892) due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia, hyperglycemia, or death.
Medtronic recalls MiniMed 630G insulin pumps (MMT-1714, MMT-1715, etc.) due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia.
Medtronic recalls MiniMed 640G insulin pumps (MMT-1711 to MMT-1752) due to potential insulin over/under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia.
Medtronic recalls MiniMed 780G insulin pumps (MMT-1884 to MMT-1896) due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia.
Medtronic recalls MiniMed 530G insulin pumps (MMT-551, MMT-751) due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia. Affected units may cause life-threatening blood sugar issues.
Medtronic recalls Paradigm REAL-Time Revel insulin pumps (MMT-523, MMT-723) due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia. Affected users should contact Medtronic for guidance.
Medtronic recalls MiniMed 740G insulin pumps (MMT-1811-1862) due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia. Affected users should contact Medtronic for guidance.
Medtronic recalls Paradigm insulin pumps (MMT-712, MMT-715) that may deliver incorrect insulin doses if moved up or down from the body, risking life-threatening blood sugar issues.
Medtronic recalls MiniMed 620G insulin pumps due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia. Affected units have specific serial numbers.
Medtronic recalls Paradigm REAL-Time Veo Insulin Pumps (MMT-554, MMT-754) due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia.
Medtronic recalls Paradigm REAL-Time Insulin Pumps (MMT-522, MMT-722) due to potential insulin over- or under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia.
Medtronic recalls MiniMed 720G insulin pumps (MMT-1809-1867) due to potential insulin over/under-delivery when pump height changes, risking severe hypoglycemia or hyperglycemia.
Medtronic MiniMed is a leading manufacturer of insulin pumps and diabetes management solutions. Their products help patients with diabetes manage their condition effectively.
Medtronic recalls InPen App version 7.5.0-8.0.0 for Android users. Uninstalling and reinstalling resets notification permissions, risking missed insulin alerts and hyperglycemia.
Medtronic recalls MiniMed 780G insulin pumps with software version 6.60 (catalog numbers MMT-1884 and MMT-1886) due to potential suspension of insulin delivery. Affected users should check their pump model and software version.
Medtronic recalls CareLink Clinic REF: MMT-7350 due to software error causing incorrect glucose data displays, which could lead to unsafe blood sugar levels. Affected users should check their device software version.
Medtronic MiniMed recalls InPen App for iOS and Android users with software versions 7.0.0-7.5.0 due to missed insulin dose reminders. This could lead to hyperglycemia if users don't receive alerts for high glucose levels. The device itself still works for insulin delivery and CGM data.
Medtronic recalls Simplera Sensor model MMT-5100JD1 due to potential infection from cap label not adhering to the sensor. Affected units sold with lot # HG81GLZ and GTIN 20763000649580.
Medtronic MiniMed recalls specific InPen smart insulin pens due to potential incorrect assembly causing insulin cartridge issues. Affected units may lead to temporary hyperglycemia without backup insulin.
Medtronic MiniMed insulin pumps (700G series) may deliver incorrect insulin during airplane takeoff or landing, risking severe hypoglycemia or death. Affected units include MMT-1801, MMT-1805, MMT-1850, MMT-1851 models.
Medtronic MiniMed insulin pumps (740G models) may deliver incorrect insulin during airplane takeoff or landing, risking severe hypoglycemia or death. Affected units include MMT-1811, MMT-1812, MMT-1861, MMT-1862.
Medtronic MiniMed 670G insulin pumps (model numbers MMT-1760 to MMT-1782) may deliver incorrect insulin during airplane takeoff or landing, risking severe hypoglycemia or hyperglycemia. Affected users should contact Medtronic for guidance.
Medtronic MiniMed recalls Paradigm insulin pumps (MMT-522, MMT-523, MMT-551, MMT-722, MMT-723, MMT-751) due to potential for abnormal insulin delivery during airplane take-off or landing, which could cause severe hypoglycemia or death.
Medtronic MiniMed recalls 640G insulin pumps (MMT-1711, MMT-1712, MMT-1751, MMT-1752) due to air pressure changes during flights causing insulin delivery issues that may lead to life-threatening blood sugar events.
Medtronic recalls Paradigm insulin pumps (all models) due to air pressure changes during flights causing potential insulin delivery issues. This could lead to severe hypoglycemia or hyperglycemia, risking life-threatening conditions. Affected users should contact Medtronic for guidance.
Medtronic MiniMed recalls insulin pumps (620G model) that may deliver incorrect insulin during airplane takeoff or landing, risking severe hypoglycemia or hyperglycemia. Affected units include all lot numbers with UDI numbers.
Medtronic MiniMed recalls Paradigm MMT-712 and MMT-715 pumps due to potential insulin delivery issues during airplane take-off or landing, which could cause severe hypoglycemia or hyperglycemia. Affected users should contact Medtronic for guidance.
Medtronic MiniMed recalls 720G insulin pumps (MMT-1809 to MMT-1867) due to air pressure changes during flights causing insulin delivery issues. This may lead to severe hypoglycemia or hyperglycemia, requiring immediate action.
Medtronic MiniMed insulin pumps (630G models) may deliver too much or too little insulin during airplane takeoff or landing, risking severe health issues. Affected units include specific model numbers and lot numbers.
Medtronic MiniMed insulin pumps (770G models) may deliver incorrect insulin during airplane takeoff or landing, risking severe hypoglycemia or hyperglycemia. Affected units include MMT-1880 to MMT-1892 series.
Medtronic recalls certain MiniMed 630G and 700G insulin pumps that may experience reduced battery life and premature shutdowns after being dropped or bumped, risking insulin delivery interruptions.
Medtronic recalls MiniMed 670G insulin pumps with certain serial numbers that may experience reduced battery life and shortened low battery alerts, potentially causing unexpected insulin delivery stops.
Medtronic recalls certain MiniMed insulin pumps that may experience reduced battery life and shortened low battery alerts after being dropped or bumped, potentially causing unexpected shutdowns and insulin delivery interruptions.
Medtronic recalls Guardian 4 Glucose Sensors with specific model numbers and lot codes due to potential glucose value errors that could cause hyperglycemia or hypoglycemia.
