Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2377-2018 — Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754

U.S. FDA — Device Enforcement · United States · 2018-04-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2377-2018
Date of alert
2018-04-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Inc.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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