Device recall
Z-2186-2012: TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical…
FDA device recall · Class III · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-2186-2012 |
|---|---|
| Recall event | 62598 |
| Product | TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body. |
| Product code | GBW |
| Recalling firm | Teleflex Medical |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 12, 2015 |
| FEI number | 3005747797 |
At a glance
- None 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