MiniMed 670G Insulin Pump: Models: PUMP MMT-1740KX 670G V6 — Class II medical device recall Z-1772-2021
Ongoing recall by Medtronic Minimed, reported 2021-06-09, distributed in AR, CA, CO, CT, FL, GA, ID, MI…. Due to a software design issue, under certain conditions, a software fault is detected when a large bolus deli
| Recall number | Z-1772-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Minimed, Northridge, CA, United States |
| Recall initiated | 2021-03-15 |
| Classified | 2021-06-01 |
| Reported by FDA | 2021-06-09 |
| Distributed | AR, CA, CO, CT, FL, GA, ID, MI, MN, TN, TX, WA |
| Countries outside the US | AT, BE, BH, CH, CL, CZ, DE, DK, EG, ES, FI, FR, GB, GR, HR, HU, IE, IL, IS, IT, LU, MT, NL, NO, PL, QA, RO, SE, SI, TR, ZA |
| Quantity | 1,266 devices |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 00763000157456, 00763000250232, 00763000258429, 00763000258436, 00763000258443, 00763000258467, 00763000303556, 00763000408909, 00763000408916, 00763000408923, 00763000408930, 00763000408947, 00763000408954 |
| Serial numbers | NG1514619H, NG1515091H, NG1515163H, NG1515522H, NG1516074H, NG1516509H, NG1517002H, NG1517803H, NG1518170H, NG1518215H, NG1518290H, NG1518680H, NG1519002H, NG1519067H, NG1519095H, NG1519563H, NG1519637H, NG1519670H, NG1519932H, NG1520477H, NG1520492H, NG1521103H, NG1521244H, NG1521322H, NG1521399H and 475 more |
| Model numbers | MMT-1740K/00763000258429, MMT-1740KX/00763000408909, MMT-1741KFX/00763000303556, MMT-1741KFX/00763000408930, MMT-1741KX/00763000258436, MMT-1741KX/00763000408916, MMT-1741KXS/00763000258443, MMT-1741KXS/00763000408923, MMT-1742KX/00763000157456, MMT-1742KX/00763000250232, MMT-1742KX/00763000258467, MMT-1742KX/00763000408947, MMT-1742KX/00763000408954 |
Product
MiniMed 670G Insulin Pump: Models: PUMP MMT-1740KX 670G V6.3 SF MG CLIN;¿ PUMP MMT-1740KX 670G V6.3 CLIN 020 MG;¿ PUMP MMT-1741KFX 670G V6.3 SF MG CLIN FR;¿ PUMP MMT-1741KFX 670G V6.3 CLIN 020 MG;¿ PUMP MMT-1741KX 670G V6.3 SF MG CLIN GER;¿ PUMP MMT-1741KX 670G V6.3 CLIN 020 MG;¿ PUMP MMT-1741KXS 670G V6.3 SF MG CLIN IS;¿ PUMP MMT-1741KXS 670G V6.3 CLIN 020 MG;¿ PUMP MMT-1742KX 670G V6.1 MM CLIN;¿ PUMP MMT-1742KX 670G V6.3 SF MM CLIN;¿ PUMP MMT-1742KX 670G V6.3 SF MM CLIN SLO;¿ PUMP MMT-1742KX 670G V6.3 CLIN 020 MM;¿ PUMP MMT-1742KX 670G V6.3 CLIN 020 EU MM;¿
Reason for recall
Due to a software design issue, under certain conditions, a software fault is detected when a large bolus delivery at quick bolus speed completes. if the user is not aware of the amount of active insulin and delivers an additional bolus, there is a risk of insulin over delivery.
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-1772-2021. 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.