Medtronic MiniMed Infusion Pumps
Medtronic MiniMed recalls Paradigm, 600, and BLE 700 series pumps over insulin delivery errors that can cause severe hypoglycemia or hyperglycemia.
Contact Medtronic MiniMed immediately to receive a replacement pump and instructions for safe use. Do not stop using your pump without consulting your healthcare provider; monitor blood glucose closely and seek emergency care for symptoms of severe hypoglycemia or hyperglycemia.
Why it was recalled
Medtronic MiniMed is recalling all Paradigm, 600 series, and BLE 700 series infusion pumps because unintended over- or under-delivery of insulin can occur when the pump is elevated or lowered relative to the infusion site due to gravitational pressure changes. Over-delivery may cause severe hypoglycemia, seizure, coma, or death; under-delivery may cause severe hyperglycemia, diabetic ketoacidosis, or death.
Is mine affected?
This recall covers 14 products. Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
| Product | UPC | Recall # |
|---|---|---|
| Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754) | 00613994717801, 00613994713834, 00613994713841, 00613994870414, 00613994870377, 00613994870407, 00643169378636, 00613994924957, 00613994717672, 00613994715531, 00613994715555, 00613994715562, 00613994409423, 00613994951502, 00643169026131, 00613994622600, 00613994407740, 00643169077737, 00643169464537, 00643169305038 | Z-1752-2026 |
| MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867) | 763000854768, 763000505196, 763000505219, 763000505318, 763000505257, 763000505295, 763000505233, 763000505370, 763000505325, 763000505332, 763000505394, 763000505356, 763000505387, 763000505349, 763000505400, 763000505226, 763000505271, 763000638016, 763000531171, 763000854751 | Z-1745-2026 |
| Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722) | 00613994409423, 00613994622600, 613994622747, 613994407733, 00613994407740, 00613994136374, 00613994271600, 00613994106476, 00613994373120, 00613994409478, 00613994312426, 00613994151780, 00885074419831, 00613994622747, 00613994951502, 00613994622648, 00643169026100, 00613994622624, 00613994622556, 00613994402011 | Z-1749-2026 |
| MiniMed 620G Insulin Pump (MMT-1750) | 643169559745, 643169721319, 763000375461, 763000253189 | Z-1747-2026 |
| Paradigm Insulin Pump (MMT-712, MMT-715) | 643169999770, 643169729360, 763000065201, 763000069001, 763000192228, 763000198602, 763000155346, 763000192143, 763000258344, 763000317140, 763000404567, 763000317188, 763000317195, 763000367046, 763000317157, 00613994470492, 00643169496262, 643169577664, 643169577688, 643169577695 | Z-1748-2026 |
| MiniMed 740G Insulin Pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862) | 763000504908, 763000504915, 763000505073, 763000484637, 763000505042, 763000504861, 763000629984, 763000504946, 763000504878, 763000559557, 763000504960, 763000505080, 763000505066, 763000629991, 763000505004, 763000504922, 763000504892, 763000505059, 763000504977, 763000505028 | Z-1746-2026 |
| MiniMed 530G Insulin Pump (MMT-551, MMT-751) | 00643169507784, 00643169736061, 00643169736092, 00643169736085, 00643169933224, 00763000161170 | Z-1751-2026 |
| MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896) | 763000411541, 763000441449, 763000523305, 763000521530, 763000521516, 763000533861, 763000544317, 763000734459, 763000758530, 763000758547, 763000578688, 763000734435, 763000504762, 763000734466, 763000924102, 763000924089, 763000454296, 763000854829, 763000411411, 763000411503 | Z-1741-2026 |
+6 more affected products. See the full list at the official source below.
Where it was sold
Distributed nationwide.
Official source
Other recent recalls from Medtronic MiniMed, Inc.
Editorial summary by Recall Canary · last updated 2026-07-28 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification