MiniMed 670G Insulin Pump (U.S
Medical device recall Z-1355-2022. 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
- 279,251 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 670G Insulin Pump (U.S. and O.U.S. Version)
279,251 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 670G (MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, MMT-1782, MMT-1760, MMT-1761, MMT-1762, MMT-1883, MMT-1893) UDI-DI Codes: 643169946040 763000278427 763000179649 643169946057 763000096984…
Every code shown here, 1,995 characters
Product Number/CFN (O.U.S. Version) MiniMed 670G (MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, MMT-1782, MMT-1760, MMT-1761, MMT-1762, MMT-1883, MMT-1893) UDI-DI Codes: 643169946040 763000278427 763000179649 643169946057 763000096984 763000190453 763000283445 763000395858 763000367084 643169939202 763000166526 763000256821 763000283506 763000283513 763000365882 643169939219 763000090203 763000190460 763000283520 763000393786 Serial Numbers: U.S. NG1839499H NG1383785H NG2337855H NG2574462H NG2148562H NG1139337H NG2507207H NG1737004H NG1259251H NG2164126H NG2591910H NG1774415H NG2450722H NG2341546H NG2394493H NG1268923H NG2059875H NG1241089H NG2909394H NG2716073H NG1188783H NG1332358H NG1805098H NG1187471H NG1928485H NG2154209H NG2562452H NG1980564H NG1844854H NG1993223H NG2208062H NG1256182H NG2108291H NG2773622H NG2840625H NG2287463H NG2116702H NG2747513H NG2006685H NG2499718H NG2256617H NG1708020H NG2473735H NG2871000H NG2031708H NG3039842H NG2843313H NG2059984H NG2440836H NG1775459H NG2154899H NG2962106H NG2844148H NG1504738H NG1777013H NG2522230H NG2783673H NG1810845H NG2787724H NG2397399H NG2752787H NG2126568H NG2003985H NG1847235H NG1639171H NG2284063H NG2613810H NG2004335H NG2112005H NG2372862H NG1596755H NG2496614H NG2640743H NG2242002H NG2344097H NG1820434H NG2035194H NG2083253H NG2583058H NG2458619H NG2383667H NG2354215H NG2253618H NG2781208H NG2244550H NG2105867H NG1965419H NG2712797H NG2491224H NG2185247H NG2581838H NG2363328H NG2603110H NG2809205H NG2463710H NG2498398H NG2497307H NG1250806H NG1451669H NG1268358H NG2514402H NG2298413H NG1276438H NG2236654H NG2159160H NG2855893H NG2860063H NG2218677H NG2113185H NG2843217H NG2713369H NG2726537H NG2823275H NG2063292H NG2495711H NG2205656H NG2514941H NG2767104H NG2180341H NG1909569H NG1926903H NG2456706H NG1130892H NG2549916H NG2546535H NG2769757H NG2811181H NG1550778H NG2321774H NG2071932H NG2264667H NG2633708H NG1795581H NG2400221H NG2293843H NG2642457H NG2542689H NG1358217H NG2878631H NG2533834H…
FDA’s list runs to 5,442,228 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 5,442,228 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.