Device recall
Z-0183-2009: Bard Vacora Biopsy Vacuum Assisted Biopsy Probe; Catalog numbers VB10118 and…
FDA device recall · Class III · Bard Peripheral Vascular Inc
Key facts
| Recall number (Z-number) | Z-0183-2009 |
|---|---|
| Recall event | 49540 |
| Product | Bard Vacora Biopsy Vacuum Assisted Biopsy Probe; Catalog numbers VB10118 and VB10140. |
| Product code | KNW |
| Recalling firm | Bard Peripheral Vascular Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 19, 2012 |
| 510(k) numbers | K062832 |
| FEI number | 2020394 |
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