MiniMed 620G Insulin Infusion Pump
Medical device recall Z-2602-2017. 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
- 6,573 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 620G Insulin Infusion Pump, Catalog No. MMT-1510, MMT-1710, MMT-1550, MMT-1750.
6,573 pumps, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Serial Number (MMT-1510) NG1010153U NG1010155U NG1010156U NG1010157U NG1010158U NG1010159U NG1010160U NG1010163U NG1010165U NG1010171U NG1010172U NG1010173U NG1010174U NG1010175U NG1010177U NG1010178U NG1010179U NG1010180U NG1010181U…
Every code shown here, 1,999 characters
Serial Number (MMT-1510) NG1010153U NG1010155U NG1010156U NG1010157U NG1010158U NG1010159U NG1010160U NG1010163U NG1010165U NG1010171U NG1010172U NG1010173U NG1010174U NG1010175U NG1010177U NG1010178U NG1010179U NG1010180U NG1010181U NG1010182U NG1010184U NG1010187U NG1010188U NG1010189U NG1010194U NG1010195U NG1010198U NG1010199U NG1010200U NG1010203U NG1010206U NG1010207U NG1010208U NG1010222U NG1010233U NG1010151U NG1010210U NG1010224U NG1010235U NG1010166U NG1010167U NG1010170U NG1010191U NG1010193U NG1010196U NG1010201U NG1010204U NG1010205U NG1010211U NG1010213U NG1010214U NG1010216U NG1010217U NG1010220U NG1010223U NG1010229U NG1010230U NG1010234U NG1010237U NG1010238U NG1010239U NG1010241U NG1010242U NG1010247U NG1010248U NG1010250U NG1010252U NG1010254U NG1010148U NG1010149U NG1010150U NG1010154U NG1010185U NG1010190U NG1010202U NG1010215U NG1010236U NG1010243U NG1010245U NG1010246U NG1010249U NG1010251U NG1010255U NG1010152U NG1010169U NG1010212U NG1010209U NG1010225U NG1010226U NG1010227U NG1010228U Serial No. for MMT-1550 NG1009635U NG1009754U NG1009767U NG1009748U NG1009702U NG1009742U NG1009745U NG1009708U NG1009743U NG1009765U NG1009747U NG1009768U NG1009763U NG1009752U NG1009762U NG1009764U NG1009744U NG1009665U NG1009727U NG1009719U NG1009739U NG1009700U NG1009707U NG1009735U NG1009728U NG1009740U NG1009741U NG1009667U NG1009687U NG1009732U NG1009712U NG1009722U NG1009675U NG1009678U NG1009718U NG1009679U NG1009713U NG1009736U NG1009677U NG1009688U NG1009674U NG1009729U NG1009690U NG1009698U NG1009691U NG1009714U NG1009703U NG1009676U NG1009750U NG1009710U NG1009701U NG1009715U NG1009898U NG1009897U NG1009902U NG1009891U NG1009896U NG1009892U NG1009916U NG1009917U NG1009914U NG1009887U NG1009893U NG1009911U NG1009904U NG1009905U NG1009890U Serial Number (MMT-1710) NG1035907H NG1035915H NG1035920H NG1035924H NG1035930H NG1035935H NG1035916H NG1035926H NG1035933H NG1035919H NG1035922H NG1003902H NG1004318H NG1003968H NG1004002H NG1004028H NG1009037H…
FDA’s list runs to 72,416 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 72,416 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.