Device recall
Z-2661-2014: Rusch, Soft Rubber (Nelaton and Nelaton Robinson), Bladder Catheter, Sterile…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-2661-2014 |
|---|---|
| Recall event | 69182 |
| Product | Rusch, Soft Rubber (Nelaton and Nelaton Robinson), Bladder Catheter, Sterile. These catheters are indicated for the routine drainage of urine from the bladder. These catheters are not intended or designed for indwelling use. |
| Product code | KOD |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 22, 2017 |
| FEI number | 3005747797 |
At a glance
- None 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