MiniMed 640G Insulin Infusion Pump
Medical device recall Z-2604-2017. Published in FDA’s Enforcement Report on Jun 28, 2017.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jun 28, 2017. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Not named no state, in where it went
- 117,239 pumps how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
MiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MMT-1752.
117,239 pumps, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Serial Number for MMT-1511 NG1009242U NG1009243U NG1009245U NG1009247U NG1009248U NG1009249U NG1009250U NG1009254U NG1009256U NG1009257U NG1009258U NG1009259U NG1009261U NG1009265U NG1009266U NG1009267U NG1009269U NG1009271U NG1009272U…
Every code shown here, 1,990 characters
Serial Number for MMT-1511 NG1009242U NG1009243U NG1009245U NG1009247U NG1009248U NG1009249U NG1009250U NG1009254U NG1009256U NG1009257U NG1009258U NG1009259U NG1009261U NG1009265U NG1009266U NG1009267U NG1009269U NG1009271U NG1009272U NG1009274U NG1009275U NG1009277U NG1009278U NG1009279U NG1009280U NG1009281U NG1009286U NG1009287U NG1009288U NG1009289U NG1009295U NG1009297U NG1009299U NG1009303U NG1009304U NG1009306U NG1009309U NG1009313U Serial Number for MMT-1711 NG1070644H NG1070700H NG1070655H NG1070689H NG1070665H NG1071450H NG1071495H NG1071520H NG1071531H NG1071367H NG1071067H NG1071076H NG1071086H NG1071097H NG1071105H NG1071133H NG1071156H NG1071170H NG1071151H NG1072180H NG1072237H NG1071273H NG1071334H NG1071338H NG1071279H NG1069437H NG1075802H NG1076744H NG1076746H NG1076747H NG1076381H NG1076722H NG1076725H NG1076726H NG1076730H NG1076716H NG1076718H NG1076727H NG1076739H NG1076719H NG1075617H NG1075642H NG1075713H NG1075747H NG1075753H NG1075777H NG1075790H NG1075815H NG1075781H NG1076743H NG1078606H NG1078607H NG1078609H NG1078610H NG1078602H NG1078084H NG1077009H NG1077019H NG1077027H NG1077031H NG1077033H NG1077754H NG1077768H NG1077786H NG1077796H NG1077800H NG1077849H NG1077810H NG1077838H NG1077862H NG1077856H NG1077861H NG1077017H NG1077025H NG1077030H NG1077777H NG1077752H NG1077782H NG1077787H NG1076717H NG1076753H NG1076758H NG1076754H NG1076769H NG1079272H NG1079307H NG1068070H NG1080697H NG1071976H NG1072055H NG1080704H NG1080725H NG1080672H NG1080676H NG1080680H NG1080685H NG1080674H NG1080677H NG1080678H NG1080679H NG1080683H NG1080717H NG1080709H NG1080723H NG1076742H NG1076772H NG1076764H NG1076768H NG1076773H NG1076745H NG1076755H NG1079310H NG1079316H NG1079319H NG1062601H NG1069261H NG1081602H NG1081615H NG1081683H NG1081686H NG1081695H NG1081698H NG1081703H NG1081715H NG1081727H NG1081735H NG1081736H NG1081759H NG1081764H NG1081678H NG1081687H NG1081718H NG1081728H NG1081749H NG1081665H NG1081657H NG1085801H NG1085816H…
FDA’s list runs to 1,404,367 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
US and OUS Angola Aruba Australia/NZ Austria Bahamas Bahrain Bangladesh Belgium Bolivia Botswana Bulgaria Cayman Islands Colombia Costa Rica Croatia Cyprus Czech Republic Denmark Dominican Republic El Salvador Estonia Faroe Islands Finland France Germany Greece Guadeloupe Guatemala Hong Kong Hungary Iceland India Iraq Ireland Israel Italy Japan Jordan Kazakhstan Kenya Korea Kuwait Latvia Lebanon Liechtenstein Lithuania Luxembourg Macedonia Malaysia Martinique Mauritius Morocco Namibia Nepal Netherlands New Caledonia Norway Oman Panama Paraguay Philippines Poland Portugal Qatar Reunion Romania San Marino Saudi Arabia Singapore Slovakia Slovenia South Africa Spain Sweden Switzerland Tanzania Thailand Trinidad and Tobago Turkey United Arab Emirates United Kingdom
These words name no state.
The words say it went outside the United States too.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on May 8, 2017.
- FDA classified it on Jun 20, 2017.
- FDA’s Enforcement Report published it on Jun 28, 2017.
- FDA terminated it on Jan 20, 2021.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Medtronic Inc., of Northridge, CA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 1,404,367 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.