CARDIOVIT AT-180 — Class II medical device recall Z-2734-2024
Ongoing recall by Schiller, Ag, reported 2024-09-04, distributed in FL. Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-
| Recall number | Z-2734-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Schiller, Ag, Baar, Switzerland |
| Recall initiated | 2024-07-24 |
| Classified | 2024-08-27 |
| Reported by FDA | 2024-09-04 |
| Distributed | FL |
| Countries outside the US | AE, AT, AU, BE, BH, CA, CH, CN, CY, CZ, DE, ES, FI, FR, GB, IE, IL, IN, IS, IT, JO, KW, LU, MA, MT, MY, NL, NO, PT, QA, RO, RS, SE, SI, ZA |
| Quantity | 1,084 untis |
| UPC / GTIN / UDI-DI | 07613365002775 |
| Model numbers | 0A.110000, 3.920570 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2734-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.