Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
Reported: July 11, 2018 Initiated: April 24, 2018 #Z-2377-2018
Product Description
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.
Details
- Recalling Firm
- Medtronic Inc.
- Units Affected
- 239,859
- Distribution
- International only. No U.S. distribution
- Location
- Northridge, CA
Frequently Asked Questions
What product was recalled? ▼
Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754. Recalled by Medtronic Inc.. Units affected: 239,859.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 11, 2018. Severity: Moderate. Recall number: Z-2377-2018.
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