FDA Device recall Z-2604-2017
MiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MMT-1752
- FDA Device
- Class II
- terminated
- Published 2017-06-28
On 2017-06-28 the FDA classified a Class II recall of MiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MMT-1752 by Medtronic, citing medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2604-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-05-08 |
| Published | 2017-06-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medtronic |
| Distribution | n/a |
Product
MiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MMT-1752.
Reason
Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
Identifiers
| code_info | Serial Number for MMT-1511 NG1009242U NG1009243U NG1009245U NG1009247U NG1009248U NG1009249U NG1009250U NG10092…Serial Number for MMT-1511 NG1009242U NG1009243U NG1009245U NG1009247U NG1009248U NG1009249U NG1009250U NG1009254U NG1009256U NG1009257U NG1009258U NG1009259U NG1009261U NG1009265U NG1009266U NG1009267U NG1009269U NG1009271U NG1009272U NG1009274U NG1009275U NG1009277U NG1009278U NG1009279U NG1009280U NG1009281U NG1009286U NG1009287U NG1009288U NG1009289U NG1009295U NG1009297U NG1009299U NG1009303U NG1009304U NG1009306U NG1009309U NG1009313U Serial Number for MMT-1711 NG1070644H NG1070700H NG1070655H NG1070689H NG1070665H NG1071450H NG1071495H NG1071520H NG1071531H NG1071367H NG1071067H NG1071076H NG1071086H NG1071097H NG1071105H NG1071133H NG1071156H NG1071170H NG1071151H NG1072180H NG1072237H NG1071273H NG1071334H NG1071338H NG1071279H NG1069437H NG1075802H NG1076744H NG1076746H NG1076747H NG1076381H NG1076722H NG1076725H NG1076726H NG1076730H NG1076716H NG1076718H NG1076727H NG1076739H NG1076719H NG1075 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2604-2017%22
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