Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version Recalled by Medtronic Inc. Due to Medtronic has identified a software anomaly that can...
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
MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected. Catalog Numbers for these insulin pumps are MMT-1510, MMT-1710, MMT-1711, MMT-1712.
Quantity: 42,215 units
Why Was This Recalled?
Medtronic has identified a software anomaly that can prevent the internal battery of the pump from charging. When the software anomaly occurs it leads to battery depletion and pump shutdown.
Where Was This Sold?
Europe, Australia, Japan, Singapore
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