Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CareLink Clinic Recalled by Medtronic MiniMed, Inc. Due to Software error causing incorrect data to be displayed...
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 Clinic, REF: MMT-7350
Quantity: 12126
Why Was This Recalled?
Software error causing incorrect data to be displayed on the 24-hour Sensor Glucose Overview Graph, any potential therapy decisions were made based on the incorrect data displayed on the 24-hour sensor glucose overview graph may lead to hypoglycemia or hyperglycemia.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic MiniMed, Inc.
Medtronic MiniMed, Inc. has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report