Drug recall
CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570
FDA recall event 95074 · Class II · Schiller, Ag
Key facts
| Event ID | 95074 |
|---|---|
| Recall numbers | Z-2734-2024 |
| Recalling firm | Schiller, Ag |
| Product type | Devices |
| Products | CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs. |
| Initiation date | Jul 24, 2024 |
| Report date | Sep 4, 2024 |
| City | Baar |
| Country | Switzerland |
| FEI number | 3002808182 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: