Reported Jun 28, 2017 · Terminated

MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.

Medtronic Inc.

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 Inc. · 18000 Devonshire St · Northridge, CA · 91325-1219

Is this the product you have?

    • MiniMed 670G Insulin Infusion Pump
    • Catalog No. MMT-1580
    • MMT-1780
    • MMT-1782
    • MMT-1760
Lot codes and dates
  • Serial Number for
    • MMT-1580
    • NG1008774U
    • NG1008781U
    • NG1008787U
    • NG1008795U
    • NG1008804U
    • NG1008814U
    • NG1008817U
    • NG1008818U
    • NG1008838U
    • NG1008871U
    • NG1008872U
    • NG1008877U
    • NG1008885U
    • NG1008886U
    • NG1008899U
    • NG1008901U
    • NG1008902U
    • NG1008915U
    • NG1008916U
    • NG1008799U
    • NG1008806U
    • NG1008834U
    • NG1008906U
    Serial Number for

    220 of 220 codes

    • MMT-1780
    • NG1014265U
    • NG1014274U
    • NG1014275U
    • NG1014279U
    • NG1014270U
    • NG1014285U
    • NG1014286U
    • NG1014271U
    • NG1014264U
    • NG1014267U
    • NG1014289U
    • NG1014684U
    • NG1014682U
    • NG1014604U
    • NG1014650U
    • NG1014651U
    • NG1014613U
    • NG1014620U
    • NG1014639U
    • NG1014616U
    • NG1014618U
    • NG1014631U
    • NG1014636U
    • NG1014659U
    • NG1014605U
    • NG1014634U
    • NG1014665U
    • NG1014633U
    • NG1014662U
    • NG1014660U
    • NG1014624U
    • NG1014623U
    • NG1014610U
    • NG1014622U
    • NG1014635U
    • NG1014637U
    • NG1014640U
    • NG1014654U
    • NG1014661U
    • NG1014666U
    • NG1016855U
    • NG1016985U
    • NG1016976U
    • NG1016984U
    • NG1016978U
    • NG1016989U
    • NG1016966U
    • NG1016990U
    • NG1016975U
    • NG1016982U
    • NG1016967U
    • NG1016979U
    • NG1016812U
    • NG1016973U
    • NG1016969U
    • NG1016971U
    • NG1016974U
    • NG1016977U
    • NG1016981U
    Serial Number for
    • MMT-1782
    • NG1017073U
    • NG1017074U
    • NG1017075U
    • NG1017076U
    • NG1017078U
    • NG1017079U
    • NG1017080U
    • NG1017081U
    • NG1017082U
    • NG1017083U
    • NG1017084U
    • NG1017085U
    • NG1017086U
    • NG1017087U
    • NG1017088U
    • NG1017089U
    • NG1017090U
    • NG1017094U
    • NG1017095U
    • NG1017096U
    • NG1017097U
    • NG1017098U
    • NG1017099U
    • NG1017100U
    • NG1017101U
    • NG1017102U
    • NG1017103U
    • NG1017104U
    • NG1017105U
    • NG1017106U
    • NG1017107U
    • NG1017108U
    • NG1017110U
    • NG1017111U
    • NG1017112U
    • NG1017115U
    • NG1017116U
    • NG1017117U
    • NG1017118U
    • NG1017119U
    • NG1017120U
    • NG1017121U
    • NG1017122U
    Serial Number

    2,423 of 2,423 codes

    • NG1229842H
    • NG1229805H
    • NG1229756H
    • NG1229774H
    • NG1229846H
    • NG1229753H
    • NG1229751H
    • NG1229794H
    • NG1229763H
    • NG1229858H
    • NG1229823H
    • NG1229814H
    • NG1229775H
    • NG1229810H
    • NG1229877H
    • NG1229788H
    • NG1229860H
    • NG1229807H
    • NG1229806H
    • NG1229745H
    • NG1229820H
    • NG1229885H
    • NG1229840H
    • NG1229872H
    • NG1229894H
    • NG1229746H
    • NG1229875H
    • NG1229821H
    • NG1229744H
    • NG1229825H
    • NG1229826H
    • NG1229844H
    • NG1229882H
    • NG1229808H
    • NG1229764H
    • NG1229816H
    • NG1229830H
    • NG1229878H
    • NG1229750H
    • NG1229761H
    • NG1229772H
    • NG1229743H
    • NG1229737H
    • NG1229783H
    • NG1229769H
    • NG1229740H
    • NG1229887H
    • NG1229760H
    • NG1229893H
    • NG1229776H
    • NG1229780H
    • NG1229862H
    • NG1229863H
    • NG1229824H
    • NG1229891H
    • NG1229881H
    • NG1229856H
    • NG1229757H
    • NG1229765H
    • NG1229849H
Amount recalled
117,239 pumps

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Why it was recalled

Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jan 20, 2021 · Data as of Sep 19, 6:07 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.