Reported Jun 9, 2021 · Ongoing
MiniMed 670G Insulin Pump: Models: PUMP MMT-1740KX 670G V6.3 SF MG CLIN;¿ PUMP MMT-1740KX 670G V6.3 CLIN 020 MG;¿ PUMP…
Medtronic Minimed
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Minimed · 18000 Devonshire St · Northridge, CA · 91325-1219
Is this the product you have?
- 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¿
- Lot codes and dates
1,279 of 1,279 products
Products covered by this recall # Barcodes Product as published 1 00763000258429MMT-1740K/00763000258429 2 00763000408909¿ MMT-1740KX/00763000408909 3 00763000303556¿ MMT-1741KFX/00763000303556 4 00763000408930¿ MMT-1741KFX/00763000408930 5 00763000258436¿ MMT-1741KX/00763000258436 6 00763000408916¿ MMT-1741KX/00763000408916 7 00763000258443¿ MMT-1741KXS/00763000258443 8 00763000408923¿ MMT-1741KXS/00763000408923 9 00763000157456¿ MMT-1742KX/00763000157456 10 00763000250232¿ MMT-1742KX/00763000250232 11 00763000258467¿ MMT-1742KX/00763000258467 12 00763000408954¿ MMT-1742KX/00763000408954 13 00763000408947¿ MMT-1742KX/00763000408947 14 Serial Numbers: NG1522406H 15 NG1698348H 16 NG2078422H 17 NG1586805H 18 NG1997312H 19 NG1829832H 20 NG1662936H - Amount recalled
- U.S. Investigational Clinical Study = 1,266 devices
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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