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Terminated

Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754

FDA Recall Z-2377-2018 · Posted 2018-07-05

Recalling FirmMedtronic Inc.
Recall StatusTerminated
Product CodeFPA
Date Initiated2018-04-24
Date Terminated2022-05-02
Product Quantity239,859

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.

Firm Action

Medtronic Inc. conducted this field corrective action via Urgent Field Safety Notification to customers: patients and health care providers.

Root Cause

Under Investigation by firm

Distribution Pattern

International only. No U.S. distribution

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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