CARDIOVIT® AT-180 Electrocardiographs
Brand(s)
Last updated
Summary
Product
CARDIOVIT® AT-180 Electrocardiographs
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Industry
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| CARDIOVIT® AT-180 | All lots. | 3.920570 |
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
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
Schiller AG
Altgasse 68, Baar, Zug, Switzerland, 6341
Published by
Health Canada
Audience
Healthcare
Industry
Recall class
Type II
Identification number
RA-75946
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