Device recall
Z-0565-2016: RenovoCath RC 120; Temporary Intravascular Occluding Catheter Model number…
FDA device recall · Class II · RenovoRx, Inc.
Key facts
| Recall number (Z-number) | Z-0565-2016 |
|---|---|
| Recall event | 72810 |
| Product | RenovoCath RC 120; Temporary Intravascular Occluding Catheter Model number: MMRC120-DB-1111; Rx only. Cardiovascular: The RenovoCath RC120 Catheter is intended for the isolation of blood flow and delivery of fluids, including diagnostic and/or therapeutic agents, to selected sites in the peripheral… |
| Product code | MJN |
| Recalling firm | RenovoRx, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 29, 2016 |
| 510(k) numbers | K141175 |
| FEI number | 3011279674 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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