MiniMed 780G Insulin Pump (O.U.S
Medical device recall Z-1359-2022. 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
- 83,398 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 780G Insulin Pump (O.U.S. Version)
83,398 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 780G (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896) UDI Codes: Pending Serial Numbers: U.S. (Clinical) NG2478545H NG2486895H NG2486985H NG2487001H NG2487055H NG2487108H NG2487112H…
Every code shown here, 1,998 characters
Product Number/CFN (O.U.S. Version) MiniMed 780G (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896) UDI Codes: Pending Serial Numbers: U.S. (Clinical) NG2478545H NG2486895H NG2486985H NG2487001H NG2487055H NG2487108H NG2487112H NG2487154H NG2487171H NG2487193H NG2487198H NG2487262H NG2487277H NG2487329H NG2487331H NG2487334H NG2487385H NG2487392H NG2487395H NG2487400H NG2487403H NG2487405H NG2487409H NG2487410H NG2487419H NG2487426H NG2487430H NG2487431H NG2487451H NG2487461H NG2487479H NG2487488H NG2487490H NG2487491H NG2487500H NG2487503H NG2487506H NG2487507H NG2487570H NG2487577H NG2487583H NG2487590H NG2487639H NG2487660H NG2487675H NG2487688H NG2487701H NG2487703H NG2487710H NG2487731H NG2487732H NG2487769H NG2487775H NG2487776H NG2487784H NG2487790H NG2487793H NG2487833H NG2487836H NG2487844H NG2487847H NG2487860H NG2487862H NG2487865H NG2487887H NG2487892H NG2487964H NG2488018H NG2488067H NG2488106H NG2488163H NG2491860H NG2491901H NG2491927H NG2491932H NG2491935H NG2491945H NG2491948H NG2491949H NG2491957H NG2491958H NG2491985H NG2492002H NG2492015H NG2492023H NG2492029H NG2492033H NG2492036H NG2492066H NG2492101H NG2492140H NG2492143H NG2492153H NG2492155H NG2492160H NG2492167H NG2492177H NG2492185H NG2492189H NG2492214H NG2492222H NG2492238H NG2492252H NG2492270H NG2492271H NG2492275H NG2492281H NG2492282H NG2492370H NG2492378H NG2492379H NG2492383H NG2492385H NG2492386H NG2492396H NG2492398H NG2492399H NG2492400H NG2492401H NG2492402H NG2492404H NG2492407H NG2492409H NG2492410H NG2492415H NG2492445H NG2492446H NG2492448H NG2492449H NG2492450H NG2492463H NG2492473H NG2492482H NG2492483H NG2492485H NG2492487H NG2492488H NG2492489H NG2492490H NG2492494H NG2492496H NG2492498H NG2492500H NG2492502H NG2492503H NG2492510H NG2492512H NG2492514H NG2492518H NG2492525H NG2492526H NG2492530H NG2492560H NG2492567H NG2492569H NG2492619H NG2492706H NG2492895H NG2586740H NG2586821H NG2586855H NG2586901H NG2589083H NG2589096H NG2589105H NG2591576H NG2591643H…
FDA’s list runs to 1,134,619 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 1,134,619 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.