Device recall
Z-0418-05: Weck Electrosurgical Coagulation Suction Tube (with stylet), REF 809600, Cannula…
FDA device recall · Class III · Weck
Key facts
| Recall number (Z-number) | Z-0418-05 |
|---|---|
| Recall event | 30639 |
| Product | Weck Electrosurgical Coagulation Suction Tube (with stylet), REF 809600, Cannula 6'' 11 French, Rx Only, Sterile, Weck A Teleflex Company, Manufactured for: Weck Closure Systems, 2917 Weck Drive, Research Triangle park, NC 27709, USA. |
| Product code | GDO |
| Recalling firm | Weck |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 31, 2005 |
| FEI number | 3005747797 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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