MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2 — Class II medical device recall Z-1890-2017
Terminated recall by Medtronic Inc., reported 2017-05-10. Medtronic has identified a software anomaly that can prevent the internal battery of the pump from charging. W
| Recall number | Z-1890-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Inc., Northridge, CA, United States |
| Recall initiated | 2017-01-31 |
| Classified | 2017-04-28 |
| Reported by FDA | 2017-05-10 |
| Terminated | 2017-05-04 |
| Countries outside the US | AU, JP, SG |
| Quantity | 42,215 units |
| Reason classes | software |
| Serial numbers | NG10, NG1000069H, NG1000070H, NG1000074H, NG1000077H, NG1000079H, NG1000080H, NG1000082H, NG1000085H, NG1000086H, NG1000088H, NG1000089H, NG1000090H, NG1000091H, NG1000093H, NG1000094H, NG1000097H, NG1000099H, NG1000101H, NG1000105H, NG1000107H, NG1000109H, NG1000110H, NG1000114H, NG1000116H and 475 more |
Product
MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected. Catalog Numbers for these insulin pumps are MMT-1510, MMT-1710, MMT-1711, MMT-1712.
Reason for recall
Medtronic has identified a software anomaly that can prevent the internal battery of the pump from charging. When the software anomaly occurs it leads to battery depletion and pump shutdown.
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-1890-2017. 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.