Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
FDA device recall Z-2377-2018 · posted 2018-07-05 · Terminated
Recall details
- Recalling firm
- Medtronic Inc.
- 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.
- Action taken
- 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
- Status
- Terminated
- Product code
- FPA
- Quantity affected
- 239,859
- Distribution
- International only. No U.S. distribution
- Date initiated
- 2018-04-24
- Date posted
- 2018-07-05
- Date terminated
- 2022-05-02
- Location
- Northridge, CA
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