MiniMed 620G Insulin Pump (O.U.S
Medical device recall Z-1352-2022. Published in FDA’s Enforcement Report on Jul 20, 2022.
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 Jul 20, 2022. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- 53 states named in where it went
- 2,287 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?
Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
MiniMed 620G Insulin Pump (O.U.S. version)
2,287 pumps, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Product Number/CFN (O.U.S. version) MiniMed 620G (MMT-1510, MMT-1710, MMT-1750) UDI Code: Pending Serial Numbers: NG1003917H NG1004461H NG1010799H NG1012557H NG1020680H NG1026110H NG1028941H NG1028949H NG1028952H NG1028973H NG1034230H…
Every code shown here, 1,995 characters
Product Number/CFN (O.U.S. version) MiniMed 620G (MMT-1510, MMT-1710, MMT-1750) UDI Code: Pending Serial Numbers: NG1003917H NG1004461H NG1010799H NG1012557H NG1020680H NG1026110H NG1028941H NG1028949H NG1028952H NG1028973H NG1034230H NG1034247H NG1034304H NG1034314H NG1034335H NG1034338H NG1034345H NG1034358H NG1034359H NG1034364H NG1034583H NG1034584H NG1034593H NG1034595H NG1034609H NG1035490H NG1035495H NG1035505H NG1035517H NG1035520H NG1035525H NG1035526H NG1035546H NG1035552H NG1035566H NG1035572H NG1035575H NG1035581H NG1035586H NG1035593H NG1035595H NG1035915H NG1035930H NG1035933H NG1035935H NG1036645H NG1036646H NG1036671H NG1036678H NG1036688H NG1036704H NG1036713H NG1036715H NG1036725H NG1036726H NG1036731H NG1036757H NG1036785H NG1036801H NG1036809H NG1036811H NG1036813H NG1036854H NG1039152H NG1040219H NG1040230H NG1040231H NG1040237H NG1040257H NG1040262H NG1040271H NG1040290H NG1040298H NG1040305H NG1040318H NG1040344H NG1040353H NG1040380H NG1040381H NG1040383H NG1040480H NG1040483H NG1040628H NG1040637H NG1040667H NG1040668H NG1040737H NG1040999H NG1041013H NG1041041H NG1041067H NG1041078H NG1041079H NG1041134H NG1041165H NG1041169H NG1041212H NG1041229H NG1041254H NG1041262H NG1043526H NG1043542H NG1043547H NG1043549H NG1043570H NG1043571H NG1043574H NG1043585H NG1043587H NG1043589H NG1043600H NG1043605H NG1043618H NG1043619H NG1043629H NG1043637H NG1043642H NG1043656H NG1043659H NG1048215H NG1051985H NG1051990H NG1052098H NG1054459H NG1054461H NG1055929H NG1055937H NG1055959H NG1055980H NG1055987H NG1056018H NG1056021H NG1056025H NG1057684H NG1057686H NG1057690H NG1059069H NG1059076H NG1059083H NG1059107H NG1059119H NG1059125H NG1059126H NG1059151H NG1059154H NG1059178H NG1059187H NG1059297H NG1059307H NG1059313H NG1059319H NG1059326H NG1059356H NG1059367H NG1059386H NG1059411H NG1059419H NG1059424H NG1059440H NG1060999H NG1066735H NG1066747H NG1066778H NG1066783H NG1066788H NG1066803H NG1066816H NG1066821H NG1066823H NG1066827H NG1066854H…
FDA’s list runs to 25,270 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.
U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VI, VT, WA, WI, WV, and WY O.U.S.: Not provided
The states and territories these words name
53 states and territories.
Every one of them
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- District of Columbia
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Puerto Rico
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- US Virgin Islands
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
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?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, 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 23, 2022.
- FDA classified it on Jul 8, 2022.
- FDA’s Enforcement Report published it on Jul 20, 2022.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Medtronic MiniMed, 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 25,270 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.