Medtronic MiniMed Paradigm Veo Insulin Pump Product
Medical device recall Z-2377-2018. Published in FDA’s Enforcement Report on Jul 11, 2018.
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 11, 2018. 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
- 239,859 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?
The MiniMed Paradigm Veo insulin pump has an error that impacts the Arabic language translation.This translation error occurs in the Predictive Alerts setting screen, which allows user to program alerts that will sound if users are predicted to reach their pre-set low or high sensor glucose values.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
239,859, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Lot Serial # PAR602720U PAR602721U PAR602727U PAR602734U PAR602736U PAR602739U PAR602740U PAR602741U PAR602743U PAR602746U PAR602747U PAR602748U PAR602750U PAR602751U PAR602755U PAR602758U PAR602759U PAR602897U PAR604895U PAR604907U…
Every code shown here, 1,993 characters
Lot Serial # PAR602720U PAR602721U PAR602727U PAR602734U PAR602736U PAR602739U PAR602740U PAR602741U PAR602743U PAR602746U PAR602747U PAR602748U PAR602750U PAR602751U PAR602755U PAR602758U PAR602759U PAR602897U PAR604895U PAR604907U PAR604917U PAR607172U PAR607201U PAR607235U PAR608710U PAR608715U PAR608724U PAR615861U PAR615862U PAR615866U PAR615869U PAR615870U PAR615871U PAR615873U PAR615878U PAR615889U PAR615894U PAR615903U PAR780320H PAR780365H PAR780392H PAR780396H PAR785836H PAR785915H PAR785925H PAR786247H PAR786265H PAR786338H PAR786340H PAR791069H PAR796167H PAR797220H PAR797230H PAR797859H PAR797907H PAR797912H PAR800371H PAR800376H PAR800392H PAR800919H PAR800934H PAR802059H PAR806151H PAR806153H PAR806157H PAR806158H PAR806159H PAR806160H PAR806162H PAR825168H PAR827543H PAR843509H PAR843510H PAR843511H PAR843512H PAR843522H PAR843525H PAR843530H PAR843531H PAR843534H PAR843535H PAR843538H PAR843539H PAR843547H PAR843551H PAR843555H PAR843556H PAR843557H PAR843580H PAR843592H PAR843593H PAR843594H PAR843595H PAR843596H PAR843597H PAR843599H PAR843601H PAR843602H PAR843603H PAR843604H PAR843605H PAR843607H PAR843610H PAR843611H PAR843612H PAR843728H PAR843739H PAR843741H PAR843749H PAR843758H PAR844361H PAR844362H PAR844365H PAR844367H PAR844368H PAR844371H PAR844372H PAR844373H PAR844375H PAR844378H PAR844381H PAR844387H PAR844477H PAR844482H PAR844484H PAR844488H PAR844494H PAR844501H PAR844971H PAR845708H PAR845785H PAR845789H PAR845792H PAR845793H PAR845795H PAR845796H PAR845797H PAR845799H PAR845800H PAR845803H PAR845805H PAR845810H PAR845811H PAR845813H PAR845817H PAR845820H PAR845826H PAR845828H PAR845831H PAR845834H PAR845837H PAR845839H PAR845840H PAR845841H PAR845844H PAR846178H PAR846179H PAR846189H PAR846208H PAR846416H PAR846425H PAR846435H PAR846472H PAR847477H PAR847480H PAR847491H PAR847492H PAR847494H PAR847500H PAR847511H PAR847512H PAR847513H PAR847515H PAR847516H PAR847518H PAR847521H PAR847524H PAR847525H PAR847533H PAR847534H…
FDA’s list runs to 46,021 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.
International only. No U.S. distribution
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 Apr 24, 2018.
- FDA classified it on Jul 5, 2018.
- FDA’s Enforcement Report published it on Jul 11, 2018.
- FDA terminated it on May 2, 2022.
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 46,021 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.