FDA Device recall Z-1743-2026
MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752)
- FDA Device
- Class II
- ongoing
- Published 2026-04-08
On 2026-04-08 the FDA classified a Class II recall of MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752) by Medtronic Minimed, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1743-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-02-13 |
| Published | 2026-04-08 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Medtronic Minimed |
| Distribution | US |
Product
MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752)
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.
Identifiers
| code_info | Pump: UDI-DI(GTIN): User Guide Name(Part-Version): MiniMed 640G Insulin Pump: 643169999763, 763000002763, 763000002671…Pump: UDI-DI(GTIN): User Guide Name(Part-Version): MiniMed 640G Insulin Pump: 643169999763, 763000002763, 763000002671, 643169999770, 763000002886, 643169729353, 763000002657, 763000002688, 763000002664, 763000002749, 763000002817, 763000002787, 763000002800, 763000002756, 763000002848, 763000002794, 763000002695, 763000002725, 763000002701, 763000002633, 763000002862, 643169729360, 763000002879, 763000002824, 763000002732, 763000002640, 763000002770, 763000002855, 763000002718, 763000002831, 763000065195, 763000065201, 763000083441, 763000015510, 763000015541, 763000015480, 763000015589, 763000015497, 763000068998, 763000015381, 763000015435, 763000015336, 763000015367, 763000069001, 763000015374, 763000015398, 763000015350, 763000192228, 763000015572, 763000015343, 763000015411, 763000015428, 763000015404, 763000015442, 763000015459, 763000015534, 763000015503, 763000194383, 763000194222, 763000194444, 763000194390, 763000194239, 763000198596, 763000194406, 763000194369, 76300001559 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1743-2026%22
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