Device recall
Z-0906-2012: AngioDynamics Morpheus Smart PICC CT 5F Dual Lumen w/ Reverse Taper 55cm --- Max…
FDA device recall · Class II · Angiodynamics Worldwide Headquarters
Key facts
| Recall number (Z-number) | Z-0906-2012 |
|---|---|
| Recall event | 60909 |
| Product | AngioDynamics Morpheus Smart PICC CT 5F Dual Lumen w/ Reverse Taper 55cm --- Max CT Flow Rate: 5mL/sec --- Catalog No.: 12110936 --- AngioDynamics, Inc., 603 Queensbury Avenue, Queensbury, NY 12804 --- Assembled and Packaged in the USA. indicated for short or long term peripheral access to the… |
| 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