Device recall
Z-1898-2009: SmartPort CT Port Access System, Catalog number CT80STPD, AngioDynamics…
FDA device recall · Class II · Angiodynamics, INC
Key facts
| Recall number (Z-number) | Z-1898-2009 |
|---|---|
| Recall event | 52762 |
| Product | SmartPort CT Port Access System, Catalog number CT80STPD, AngioDynamics Incorporated The SmartPort CT Port Access System is indicated for any patient requiring repeated access of the vascular system or other selected body site, for delivery of medications, nutritional supplementation, fluids, blood… |
| Product code | LJT |
| Recalling firm | Angiodynamics, INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 27, 2010 |
| 510(k) numbers | K081472 |
| 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