# FDA recall Z-2734-2024

> **Schiller, Ag** · Class II · device recall initiated 2024-07-24.

## Product

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

## Reason for recall

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

## 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.

## Key facts

- **Recall number:** Z-2734-2024
- **Recalling firm:** Schiller, Ag
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-24
- **Report date:** 2024-09-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Baar, Switzerland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2734-2024

## Citation

> AI Analytics. FDA recall Z-2734-2024. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-2734-2024. Source: US FDA. Licensed CC0.

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