Device recall
Z-2782-2011: Site Rite Vision Ultrasound System, REF 9770032, Bard Access Systems, Inc…
FDA device recall · Class II · Bard Access Systems
Key facts
| Recall number (Z-number) | Z-2782-2011 |
|---|---|
| Recall event | 57012 |
| Product | Site Rite Vision Ultrasound System, REF 9770032, Bard Access Systems, Inc. Intended for diagnostic ultrasound imaging or fluid flow analysis of the human body. |
| Product code | IYN |
| Recalling firm | Bard Access Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 11, 2012 |
| 510(k) numbers | K100402 |
| FEI number | 3006260740 |
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