---
title: "CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570 — FDA record Z-2734-2024 | Is It on Recall"
description: "Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs."
url: https://isitonrecall.com/recall/fda-device-z-2734-2024-cardiovit-at-180-model-number-0a-110000-catalog-number-3-920570/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570 — FDA record Z-2734-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 24, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570
- **Reason**: Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.
- **Classification**: Class II
- **Recalling firm**: Schiller, Ag
- **Quantity**: 1084 untis
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2734-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2734-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: 07613365002775. All serial numbers, all software versions. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide - US distribution in the state of Florida and the countries of Austria, Belgium, Switzerland, Cyprus, Czechia, Germany, Spain, Finland, France, Great Britain, Ireland, Iceland, Italy, Luxembourg, Malta, The Netherlands, Norway, Portugal, Romania, Sweden, Slovenia, Australia, The United Arab Emirates, Bahrain, Canada, China, Israel, India, Jordan, Kuwait, Libya, Morocco, Malaysia, Qatar, Serbia, South Africa.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Florida](https://isitonrecall.com/state/florida/)

## Dates in the source

- **Report date**: Sep 4, 2024
- **Recall initiation date**: Jul 24, 2024
- **Center classification date**: Aug 27, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2734-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Schiller, Ag records](https://isitonrecall.com/brand/schiller-ag/)