Device recall
Z-1661-2013: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite System is a…
FDA device recall · Class II · DJO, LLC
Key facts
| Recall number (Z-number) | Z-1661-2013 |
|---|---|
| Recall event | 65493 |
| Product | VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite System is a compression pump used for the prevention of Deep Vein Thrombosis. |
| Product code | JOW |
| Recalling firm | DJO, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 13, 2014 |
| 510(k) numbers | K091700 |
| FEI number | 2020737 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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