Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T,…
Medical device recall Z-0107-2018. Published in FDA’s Enforcement Report on Nov 29, 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 Nov 29, 2017. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Not named no state, in where it went
- 3,971,030 units 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(TM) Infusion Sets have the potential for over-delivery of Insulin.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)
3,971,030 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Lot Numbers: 5179671 5179672 5179675 5179676 5179678 5179680 5174468 5174471 5185640 5185642 5185643 5185645 5185647 5185648 5185650 5176067 5176070 5176073 5176074 5176079 5176082 5176085 5185660 5185663 5185666 5185669 5185672 5185673…
Every code shown here, 1,997 characters
Lot Numbers: 5179671 5179672 5179675 5179676 5179678 5179680 5174468 5174471 5185640 5185642 5185643 5185645 5185647 5185648 5185650 5176067 5176070 5176073 5176074 5176079 5176082 5176085 5185660 5185663 5185666 5185669 5185672 5185673 5176224 5176050 5176052 5176054 5176056 5189836 5189838 5189839 5173751 5173752 5189378 5189379 5189380 5174455 5174457 5174459 5174461 5189358 5189359 5189362 5189364 5189366 5185736 5174481 5174483 5174485 5174487 5189386 5189388 5189390 5189392 5189394 5189395 5179685 5179686 5179687 5179688 5179689 5170715 5170823 5170825 5170827 5173463 5174300 5173470 5173471 5173472 5173473 5173474 5173475 5173476 5173477 5170133 5170134 5170135 5179710 5179711 5179712 5179713 5179714 5179715 5179716 5179717 5179718 5179719 5179720 5179721 5179722 5179723 5179724 5179725 5179726 5179727 5179728 5170153 5170154 5170155 5179690 5179691 5179692 5179693 5179694 5179695 5179696 5179697 5179698 5179699 5179700 5179701 5179702 5179703 5179704 5179705 5175939 5175940 5176014 5176015 5176016 5176017 5176018 5176019 5176020 5176021 5176022 5176023 5176024 5176025 5180499 5180500 5180501 5180502 5180503 5180504 5180505 5180506 5180507 5180508 5180509 5180510 5180511 5180512 5180513 5180514 5180515 5180516 5180517 5180518 5185600 5185601 5185602 5185603 5185604 5185605 5185606 5185607 5185608 5185609 5185610 5185611 5185612 5185613 5185614 5185615 5185616 5185617 5185618 5185619 5188097 5188098 5188099 5188100 5188101 5188102 5188103 5188104 5188105 5188106 5188107 5188108 5188109 5188110 5188111 5188112 5188113 5188114 5188115 5189846 5189847 5189852 5189853 5171629 5171630 5171631 5171632 5171633 5171634 5171635 5171636 5171637 5171638 5171639 5171640 5171641 5171642 5171643 5171644 5171645 5171646 5171647 5171648 5176026 5176027 5176028 5176029 5176030 5176031 5176032 5176033 5176034 5176035 5176036 5176037 5176038 5176039 5176040 5176041 5176042 5176043 5176044 5176045 5179790 5179791 5179792 5179793 5179794 5179795 5179796 5179797 5179798 5179799…
FDA’s list runs to 4,204 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.
Worldwide
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?
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 Sep 10, 2017.
- FDA classified it on Nov 18, 2017.
- FDA’s Enforcement Report published it on Nov 29, 2017.
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: Press Release.
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 4,204 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.