Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic MiniMed is recalling the CareLink iPro Therapy...
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
CareLink iPro Version 1.10, Catalog No. MMT-7340 With data obtained from the iPro2 recorder and blood glucose meter, the CareLink iPro software retrospectively calibrates sensor data and provides reports of continuous glucose information. CareLink iPro reports show up to seven calendar days of study data. The reports are created in PDF format, so they can easily be printed or stored electronically.
Quantity: 33 units
Why Was This Recalled?
Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software due to a time stamp error.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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