Device recall
Z-0744-04: Acuson Cypress Echocardiography System
FDA device recall · Class III · Siemans Medial Solutions USA, Inc
Key facts
| Recall number (Z-number) | Z-0744-04 |
|---|---|
| Recall event | 28393 |
| Product | Acuson Cypress Echocardiography System |
| Product code | IYN |
| Recalling firm | Siemans Medial Solutions USA, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 19, 2004 |
| 510(k) numbers | K021497 |
| FEI number | 3002626007 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database