Medical DeviceFeb 25, 2015
Alivecor SFO Alive ECG App 2.1.2 recall — FDA Z-1125-2015
Alive ECG App version 2.1.2 (intended to be used with the AliveCor Heart Monitor) crashed upon use of the application.
Class IIIFDA: TerminatedAlivecor SFO
Recall history in this database
Classification mix: Class III: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Alivecor SFO as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.