Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CareLink iPro2 Reports Recalled by Medtronic MiniMed Inc. Due to Medtronic MiniMed is recalling 19 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 MiniMed Inc. directly.
Affected Products
CareLink iPro2 Reports, Model No. MMT-7340 is software intended to retrospectively calibrates sensor data and provides reports of continuous glucose information
Quantity: 20
Why Was This Recalled?
Medtronic MiniMed is recalling 19 CareLink iPro Therapy Management reports because the CareLink iPro reports were created using the Pacific Standard Time zone as the time reference, although the patients and their sensor data were subject to the Central Standard Time zone. The CareLink iPro2 Professional CGM (continuous glucose monitor) data uploading error that resulted in an inaccurate time zone being applied to 19 CareLink iPro reports.
Where Was This Sold?
This product was distributed to 1 state: MN
About Medtronic MiniMed Inc.
Medtronic MiniMed Inc. has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report