Reported Sep 4, 2024 · Ongoing

CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570

Schiller, Ag

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Schiller, Ag · Altgasse 68 · Baar · N/A

Is this the product you have?

  • CARDIOVIT AT-180
  • Model Number0A.110000
  • Catalog number3.920570
Lot codes and dates
  • UDI-DI07613365002775. All serial numbers, all software versions
Amount recalled
1084 untis

Where it was sold

Why it was recalled

Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:39 PM UTC

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