Product Wiki · Recalls · Health Canada — Medical Devices

CARDIOVIT® AT-180 Electrocardiographs — recall 75946

Health Canada — Medical Devices · Canada · 2024-08-20 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
75946
Date of alert
2024-08-20
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Cardiovascular
Product type
Medical devices
Reported risk: 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
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/cardiovitr-180-electrocardiogr

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