FDA Device recall Z-2605-2017
MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760
- FDA Device
- Class II
- terminated
- Published 2017-06-28
On 2017-06-28 the FDA classified a Class II recall of MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760 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-2605-2017 |
| 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 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.
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-1580 NG1008774U NG1008781U NG1008787U NG1008795U NG1008804U NG1008814U NG1008817U NG10088…Serial Number for MMT-1580 NG1008774U NG1008781U NG1008787U NG1008795U NG1008804U NG1008814U NG1008817U NG1008818U NG1008838U NG1008871U NG1008872U NG1008877U NG1008885U NG1008886U NG1008899U NG1008901U NG1008902U NG1008915U NG1008916U NG1008799U NG1008806U NG1008834U NG1008906U Serial Number for MMT-1780 NG1014265U NG1014274U NG1014275U NG1014279U NG1014270U NG1014285U NG1014286U NG1014271U NG1014264U NG1014267U NG1014289U NG1014684U NG1014682U NG1014604U NG1014650U NG1014651U NG1014613U NG1014620U NG1014639U NG1014616U NG1014618U NG1014631U NG1014636U NG1014659U NG1014605U NG1014634U NG1014665U NG1014633U NG1014662U NG1014660U NG1014624U NG1014623U NG1014610U NG1014622U NG1014635U NG1014637U NG1014640U NG1014654U NG1014661U NG1014666U NG1016855U NG1016985U NG1016976U NG1016984U NG1016978U NG1016989U NG1016966U NG1016990U NG1016975U NG1016982U NG1016967U NG1016979U NG1016812U NG1016973U NG1016969U NG1016 |
|---|
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-2605-2017%22
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