Back to RecallTracker
Health Canada Medical devices

CARDIOVIT® AT-180 Electrocardiographs

Issued August 20, 2024
Issue
Occasionally high-frequency signal artifacts are recorded during an ECG acquisition performed by CARDIOVIT® AT-180 electrocardiographs. It has been observed that these high-frequency artifacts have been occasionally incorrectly identified as pacemaker spikes by the electrocardiograph. Recall start date: July 24, 2024
Hazard description
Performance
Product
Product name
CARDIOVIT® AT-180 Electrocardiographs
Reference
ID
RA-75946