Schiller recalls Cardiovit AT-180 electrocardiographs due to potential high-frequency signal artifacts during ECG readings. Affected units have model 0A.110000 and catalog number 3.920570.
Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.
Schiller is recalling all Cardiovit AT-180 electrocardiographs with model number 0A.110000 and catalog number 3.920570 because they may cause signal artifacts during ECG readings. This could lead to inaccurate heart monitoring results.
The Cardiovit AT-180 may produce high-frequency signal artifacts during ECG acquisitions. This can cause inaccurate heart monitoring readings, potentially leading to incorrect medical decisions.
Healthcare professionals using the Cardiovit AT-180 electrocardiographs are most at risk. Patients receiving ECG monitoring with these devices may experience inaccurate results.
Check for model number 0A.110000 and catalog number 3.920570 on the device. All serial numbers and software versions are affected.
Identify the model number (0A.110000) and catalog number (3.920570) on your Cardiovit AT-180 electrocardiograph.
The recall is for potential signal artifacts during ECG readings, which could lead to inaccurate heart monitoring. However, no injuries have been reported, and the risk is considered low.
Check for model number 0A.110000 and catalog number 3.920570 on your Cardiovit AT-180 electrocardiograph. All serial numbers and software versions are affected.
The recall does not specify a remedy, so no action is required beyond checking if your device matches the affected model and catalog numbers.
We’ve drafted a message you can send Schiller to request your refund or repair — edit it as you like.
Subject: Recall Z-2734-2024 — Schiller Schiller Hello, I own a Schiller that is covered by recall Z-2734-2024 from Schiller. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
