FDA Device recall Z-2260-2015
MiniMed NGP 640G 1.8ml (mmol/L), Model No. MMT-1511
- FDA Device
- Class II
- terminated
- Published 2015-08-05
On 2015-08-05 the FDA classified a Class II recall of MiniMed NGP 640G 1.8ml (mmol/L), Model No. MMT-1511 by Medtronic Minimed, citing medtronic MiniMed is recalling the MiniMed 620G and 640G insulin pumps because there are certain scenarios where the set Bolus screen will not timeout, which could cause confusion….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2260-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-06-19 |
| Published | 2015-08-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Medtronic Minimed |
| Distribution | n/a |
Product
MiniMed NGP 640G 1.8ml (mmol/L), Model No. MMT-1511; NGP 640G 1.8ml (mg/dL), Model No. 1512; NGP 640G PLGM 3ml (mmol/L), Model No. MMT-1711; NGP 640G PLGM 3ml (mg/dL), Model No. MMT-1712.
Reason
Medtronic MiniMed is recalling the MiniMed 620G and 640G insulin pumps because there are certain scenarios where the set Bolus screen will not timeout, which could cause confusion by showing a bolus amount that is no longer appropriate.
Identifiers
| code_info | n/a |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2260-2015%22
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