Device recall
Z-0975-03: Acuson Cypress Echocardiography System. Imaging System
FDA device recall · Class II · Siemans Medial Solutions USA, Inc
Key facts
| Recall number (Z-number) | Z-0975-03 |
|---|---|
| Recall event | 26456 |
| Product | Acuson Cypress Echocardiography System. Imaging System |
| Product code | IYN |
| Recalling firm | Siemans Medial Solutions USA, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 16, 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