Medtronic MiniMed, Inc.

Frequent Recalls

15

Recalls

0

Units Recalled

0

Injuries

0

Deaths

1 category · 2026-04-01 to 2026-04-08

Date	Source	Product	Brand	Severity	Units
2026-04-08	FDA Device	FDA Recall: MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: MiniMed 620G Insulin Pump (MMT-1750)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Paradigm Insulin Pump (MMT-712, MMT-715)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: MiniMed 740G Insulin Pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: Paradigm REAL-Time Revel Insulin Pump (MMT-523, MMT-723)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: MiniMed 530G Insulin Pump (MMT-551, MMT-751)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-08	FDA Device	FDA Recall: MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)	Medtronic MiniMed, Inc.	Class II	N/A
2026-04-01	FDA Device	FDA Recall: MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61	Medtronic MiniMed, Inc.	Class II	N/A