Device recall
Z-0999-2009: Viasys Healthcare, Sonora Transcranial Doppler (TCD) System. Model Sonara. Part…
FDA device recall · Class II · Cardinal Health, Inc
Key facts
| Recall number (Z-number) | Z-0999-2009 |
|---|---|
| Recall event | 50875 |
| Product | Viasys Healthcare, Sonora Transcranial Doppler (TCD) System. Model Sonara. Part Number of Units: 982A0470 Sonara Bilateral. The Sonara Transcranial Doppler system is a medical ultrasound device for noninvasively measuring the blood flow velocities in arteries and veins. |
| Product code | IYN |
| Recalling firm | Cardinal Health, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 3, 2012 |
| 510(k) numbers | K060421 |
| FEI number | 3010611950 |
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