FDA Device recall Z-2377-2018
Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
- FDA Device
- Class II
- terminated
- Published 2018-07-11
On 2018-07-11 the FDA classified a Class II recall of Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754 by Medtronic, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2377-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-04-24 |
| Published | 2018-07-11 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medtronic |
| Distribution | n/a |
Product
Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
Reason
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.
Identifiers
| code_info | Lot Serial # PAR602720U PAR602721U PAR602727U PAR602734U PAR602736U PAR602739U PAR602740U PAR602741U PAR602743…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 PA |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2377-2018%22
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