Device recall
Z-0884-2012: AngioDynamics Morpheus Smart PICC CT 55cm 6F Dual Lumen with REVERSE TAPER…
FDA device recall · Class II · Angiodynamics Worldwide Headquarters
Key facts
| Recall number (Z-number) | Z-0884-2012 |
|---|---|
| Recall event | 60909 |
| Product | AngioDynamics Morpheus Smart PICC CT 55cm 6F Dual Lumen with REVERSE TAPER --- Max CT Flow Rate: 5mL/SEC --- Injector Pressure Limit: 300 PSI --- Catalog No. [REF] 12102617 --- Made in the USA --- [Manufacturing symbol] AngioDynamics, 603 Queensbury Avenue, Queensbury, NY USA 12804 indicated for… |
| Product code | LJS |
| Recalling firm | Angiodynamics Worldwide Headquarters |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2016 |
| 510(k) numbers | K093406 |
| FEI number | 3008319439 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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