Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number:… — Class II medical device recall Z-2377-2018
Terminated recall by Medtronic Inc., reported 2018-07-11. The MiniMed Paradigm Veo insulin pump has an error that impacts the Arabic language translation.This translati
| Recall number | Z-2377-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Inc., Northridge, CA, United States |
| Recall initiated | 2018-04-24 |
| Classified | 2018-07-05 |
| Reported by FDA | 2018-07-11 |
| Terminated | 2022-05-02 |
| Quantity | 239,859 |
| Serial numbers | 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 and 475 more |
| Model numbers | MMT-554, MMT-754 |
Product
Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2377-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.