Device recall
Z-0604-2009: MassTRANSIT Infusion Catheter Kit, 605-731K & 605-780K, Cordis Neurovascular…
FDA device recall · Class II · Cordis Corporation
Key facts
| Recall number (Z-number) | Z-0604-2009 |
|---|---|
| Recall event | 50154 |
| Product | MassTRANSIT Infusion Catheter Kit, 605-731K & 605-780K, Cordis Neurovascular Intended to be used as a mechanism for the infusion of various diagnostic, embolic, and therapeutic agents into the Neurovascular, Peripheral Vascular and Coronary Vascular systems and for superselective angiography of… |
| Product code | KRA |
| Recalling firm | Cordis Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 2, 2009 |
| 510(k) numbers | K983003 |
| FEI number | 1016427 |
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