Device recall
Z-2940-2011: RUSCH, GB: Robinson/Nelaton Catheter, All Purpose PVC 16 Fr. 40 cm, Distributed…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-2940-2011 |
|---|---|
| Recall event | 59356 |
| Product | RUSCH, GB: Robinson/Nelaton Catheter, All Purpose PVC 16 Fr. 40 cm, Distributed by Teleflex Medical, Research Triangle Park, NC. Product Usage: Catheter that is inserted through the urethra and used to pass fluids to or from the urinary tract. |
| Product code | KOD |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 29, 2014 |
| 510(k) numbers | K896729 |
| FEI number | 3005747797 |
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