Device recall
Z-3071-2011: Vortex MP Port Single Titanium Port with Attached (5Fr) Silicone Catheter…
FDA device recall · Class II · Angiodynamics, INC
Key facts
| Recall number (Z-number) | Z-3071-2011 |
|---|---|
| Recall event | 59680 |
| Product | Vortex MP Port Single Titanium Port with Attached (5Fr) Silicone Catheter, AngioDynamics, Inc., One Horizon Way, Manchester, GA 30816 Indicated for central venous placement (either peripheral or chest placement) when patient therapy requires repeated venous access for injection or infusion therapy… |
| Product code | LJT |
| Recalling firm | Angiodynamics, INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 12, 2012 |
| 510(k) numbers | K033473 |
| FEI number | 3017892510 |
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