FDA Device recall Z-2603-2017
MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755
- FDA Device
- Class II
- terminated
- Published 2017-06-28
On 2017-06-28 the FDA classified a Class II recall of MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755 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-2603-2017 |
| 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 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.
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-1715 NG1140728H NG1139298H NG1139381H NG1140796H NG1134567H NG1140699H NG1134599H NG11389…Serial Number for MMT-1715 NG1140728H NG1139298H NG1139381H NG1140796H NG1134567H NG1140699H NG1134599H NG1138989H NG1139013H NG1140756H NG1140754H NG1139436H NG1138977H NG1139321H NG1140735H NG1139306H NG1141105H NG1139051H NG1141017H NG1139356H NG1141025H NG1139089H NG1138990H NG1139344H NG1140994H NG1139190H NG1140781H NG1140693H NG1140785H NG1139390H NG1139103H NG1139023H NG1140987H NG1140959H NG1140743H NG1139131H NG1139349H NG1139377H NG1139338H NG1140773H NG1139316H NG1139285H NG1139144H NG1139308H NG1139347H NG1140766H NG1139266H NG1139031H NG1134462H NG1140997H NG1140981H NG1140973H NG1140998H NG1141044H NG1139348H NG1140757H NG1140719H NG1141024H NG1140723H NG1140718H NG1140967H NG1140999H NG1140731H NG1140770H NG1140957H NG1140762H NG1140784H NG1140720H NG1139339H NG1140708H NG1141003H NG1140901H NG1140880H NG1140811H NG1140747H NG1139290H NG1139352H NG1140710H NG1139293H NG1139312H NG1139301H |
|---|
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-2603-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.