# FDA recall Z-2377-2018

> **Medtronic Inc.** · Class II · device recall initiated 2018-04-24.

## 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.

## Distribution

International only. No U.S. distribution

## Key facts

- **Recall number:** Z-2377-2018
- **Recalling firm:** Medtronic Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-04-24
- **Report date:** 2018-07-11
- **Termination date:** 2022-05-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northridge, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2377-2018

## Citation

> AI Analytics. FDA recall Z-2377-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2377-2018. Source: US FDA. Licensed CC0.

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