FDA Device recall Z-1772-2021
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.…
- FDA Device
- Class II
- ongoing
- Published 2021-06-09
On 2021-06-09 the FDA classified a Class II recall of 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.… by Medtronic Minimed, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1772-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-03-15 |
| Published | 2021-06-09 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medtronic Minimed |
| Distribution | AR, CA, CO, CT, FL, GA, ID, MI, MN, TN, TX, WA |
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
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.
Identifiers
| code_info | Model #(CFN)/¿UDI-DI(GTIN): MMT-1740K/00763000258429;¿ MMT-1740KX/00763000408909;¿ MMT-1741KFX/00763000303556;¿ MMT…Model #(CFN)/¿UDI-DI(GTIN): 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/00763000408954;¿ MMT-1742KX/00763000408947; Serial Numbers: NG1522406H; NG1698348H; NG2078422H; NG1586805H; NG1997312H; NG1829832H; NG1662936H; NG2127163H; NG1899556H; NG1687796H; NG1830512H; NG1560426H; NG1998243H; NG1984224H; NG1556256H; NG1998843H; NG1522295H; NG1937812H; NG1541556H; NG1829747H; NG2062114H; NG1531199H; NG1570173H; NG1713497H; NG2006526H; NG2006970H; NG1733793H; NG2006078H; NG1703340H; NG2020531H; NG1898154H; NG1932186H; NG2001204H; NG1733151H; NG1700186H; NG1731830H; NG1831300H; NG1995586H; NG2003110H; NG1830451H; NG1900348H; NG1830644H; NG1686683H; NG1560375H; N |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1772-2021%22
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