Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554 Recalled by Medtronic Inc. Due to The MiniMed Paradigm Veo insulin pump has an...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Inc. directly.
Affected Products
Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
Quantity: 239,859
Why Was This 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.
Where Was This Sold?
International only. No U.S. distribution
About Medtronic Inc.
Medtronic Inc. has 85 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report