Official recall record
CARDIOVIT® AT-180 Electrocardiographs
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-08-20
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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