Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Alive ECG App 2.1.2 ( a medical device application for Recalled by Alivecor SFO Due to Alive ECG App version 2.1.2 (intended to be...
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 Alivecor SFO directly.
Affected Products
Alive ECG App 2.1.2 ( a medical device application for the Apple iOS operating system, intended to be used with the AliveCor Heart Monitor. The AliveCor Heart Monitor is intended to record, store and transfer single-channel electrocardiogram (ECG) rhythms. The AliveCor Heart Monitor also displays ECG rhythms and detects the presence of atrial fibrillation and normal sinus rhythm (when prescribed or used under the care of a physician).
Quantity: 5600 active users with Alive ECG app for iOS .
Why Was This Recalled?
Alive ECG App version 2.1.2 (intended to be used with the AliveCor Heart Monitor) crashed upon use of the application.
Where Was This Sold?
Downloaded by Apple users - locations not shared by Apple.
About Alivecor SFO
Alivecor SFO has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report