Device recall
Z-0056-2012: 8F Smart Port CT, Catalog number: CT80STPD and CT80STPD-NF; AngioDynamics, INC…
FDA device recall · Class II · Angiodynamics, INC
Key facts
| Recall number (Z-number) | Z-0056-2012 |
|---|---|
| Recall event | 59526 |
| Product | 8F Smart Port CT, Catalog number: CT80STPD and CT80STPD-NF; AngioDynamics, INC. The Smart Port CT Implantable Port is a Single Titanium Port System with Attachable 8.0 Fr. Polyurethane Catheters and 8Fr. Introducer Kit. |
| Product code | DYB |
| Recalling firm | Angiodynamics, INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 7, 2012 |
| 510(k) numbers | K062414 |
| 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