FDA Device recall Z-2734-2024
CARDIOVIT AT-180
- FDA Device
- Class II
- ongoing
- Published 2024-09-04
On 2024-09-04 the FDA classified a Class II recall of CARDIOVIT AT-180 by Schiller Ag, citing potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2734-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-07-24 |
| Published | 2024-09-04 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Schiller Ag |
| Distribution | FL |
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.
Identifiers
| code_info | UDI-DI: 07613365002775. All serial numbers, all software versions. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2734-2024%22
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