Device recall
Z-0467-2012: MORPHEUS CT PICC with STYLET, 5F Dual Lumen 65 cm Insertion Kit, Catalog No./REF…
FDA device recall · Class III · Angiodynamics Worldwide Headquarters
Key facts
| Recall number (Z-number) | Z-0467-2012 |
|---|---|
| Recall event | 60590 |
| Product | MORPHEUS CT PICC with STYLET, 5F Dual Lumen 65 cm Insertion Kit, Catalog No./REF 1200923, STERILE, AngioDynamics Queensbury, NY 12804 USA --- COMMON/USUAL NAME: Percutaneous, implanted, long-term intravascular catheter; CLASSIFICATION NAME: Percutaneous, implanted, long-term intravascular catheter… |
| Product code | LJS |
| Recalling firm | Angiodynamics Worldwide Headquarters |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 27, 2012 |
| 510(k) numbers | K030415 |
| FEI number | 3008319439 |
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