MiniMed NGP 640G 1 — Class II medical device recall Z-2260-2015
Terminated recall by Medtronic MiniMed Inc., reported 2015-08-05. Medtronic MiniMed is recalling the MiniMed 620G and 640G insulin pumps because there are certain scenarios whe
| Recall number | Z-2260-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic MiniMed Inc., Northridge, CA, United States |
| Recall initiated | 2015-06-19 |
| Classified | 2015-07-24 |
| Reported by FDA | 2015-08-05 |
| Terminated | 2015-10-02 |
| Countries outside the US | AU, CZ, DK, FI, FR, GB, IE, NL, NO, SE |
| Quantity | 1,936 units |
| Model numbers | 1512, MMT-1511, MMT-1711, MMT-1712 |
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2260-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.