MiniMed 630G Insulin Infusion Pump
Medical device recall Z-2603-2017. 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
- 65,959 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 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.
65,959 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-1715 NG1140728H NG1139298H NG1139381H NG1140796H NG1134567H NG1140699H NG1134599H NG1138989H NG1139013H NG1140756H NG1140754H NG1139436H NG1138977H NG1139321H NG1140735H NG1139306H NG1141105H NG1139051H NG1141017H…
Every code shown here, 1,996 characters
Serial Number for MMT-1715 NG1140728H NG1139298H NG1139381H NG1140796H NG1134567H NG1140699H NG1134599H NG1138989H NG1139013H NG1140756H NG1140754H NG1139436H NG1138977H NG1139321H NG1140735H NG1139306H NG1141105H NG1139051H NG1141017H NG1139356H NG1141025H NG1139089H NG1138990H NG1139344H NG1140994H NG1139190H NG1140781H NG1140693H NG1140785H NG1139390H NG1139103H NG1139023H NG1140987H NG1140959H NG1140743H NG1139131H NG1139349H NG1139377H NG1139338H NG1140773H NG1139316H NG1139285H NG1139144H NG1139308H NG1139347H NG1140766H NG1139266H NG1139031H NG1134462H NG1140997H NG1140981H NG1140973H NG1140998H NG1141044H NG1139348H NG1140757H NG1140719H NG1141024H NG1140723H NG1140718H NG1140967H NG1140999H NG1140731H NG1140770H NG1140957H NG1140762H NG1140784H NG1140720H NG1139339H NG1140708H NG1141003H NG1140901H NG1140880H NG1140811H NG1140747H NG1139290H NG1139352H NG1140710H NG1139293H NG1139312H NG1139301H NG1139330H NG1140846H NG1140979H NG1140704H NG1140694H NG1139346H NG1139371H NG1141015H NG1141011H NG1139174H NG1140974H NG1139313H NG1140721H NG1139353H NG1139329H NG1139263H NG1139420H NG1140985H NG1140733H NG1139397H NG1140966H NG1139322H NG1141026H NG1140726H NG1140697H NG1139167H NG1140970H NG1139304H NG1140806H NG1139265H NG1141012H NG1139182H NG1139279H NG1138905H NG1139439H NG1139288H NG1138983H NG1140993H NG1139171H NG1139159H NG1139358H NG1140782H NG1140763H NG1140774H NG1140771H NG1140963H NG1140729H NG1139296H NG1140765H NG1140790H NG1140792H NG1140740H NG1141033H NG1140705H NG1141010H NG1139320H NG1139319H NG1139345H NG1139196H NG1139282H NG1140951H NG1139317H NG1140698H NG1139379H NG1139362H NG1140724H NG1140761H NG1140727H NG1139354H NG1140700H NG1140703H NG1140938H NG1140707H NG1139026H NG1140701H NG1140709H NG1140702H NG1140713H NG1140760H NG1140742H NG1140744H NG1140715H NG1141023H NG1141064H NG1140714H NG1141062H NG1140730H NG1140956H NG1140725H NG1139307H NG1134491H NG1140984H NG1140780H NG1140989H NG1134602H NG1140769H NG1140983H NG1140949H…
FDA’s list runs to 788,871 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 788,871 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
-
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.