Medtronic MiniMed, Inc. recalls
23 recalls.
- Generic Name: MiniMed Go App Generic Name: MiniMed Go App Model/Catalog Number: MMT-8600 recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported October 28, 2026 · A software defect in which existing users who had previously configured and enabled the long-acting dose reminder feature in version 1.2.0 or earlier... - CareLink Clinic recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported October 28, 2026 · CareLink Clinic software version 4.4A includes a software defect in the Settings Calculator feature in which the calculation logic fails to use custom values... - Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog... recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported October 14, 2026 · Some MiniMed Flex insulin pumps were released with missing (i.e., devices with no result or abort test results are presumed to have failed) or failed... - MiniMed 780G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported August 26, 2026 · Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result... - MiniMed 670G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported August 26, 2026 · Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result... - MiniMed 640G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported August 26, 2026 · Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result... - MiniMed Go App recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported July 29, 2026 · For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the... - MiniMed 780G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported July 15, 2026 · A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and... - Paradigm REAL-Time Veo Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed 530G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - Paradigm REAL-Time Revel Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - Paradigm REAL-Time Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - Paradigm Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed 620G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed 740G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed 720G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed 700G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed 640G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed 770G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed 780G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed 630G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed 670G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · 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... - MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61 recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 1, 2026 · Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61...