Device recall
Z-0826-2015: WECK Hemoclip Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0826-2015 |
|---|---|
| Recall event | 69918 |
| Product | WECK Hemoclip Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended for use in procedures involving vessels or anatomic structures for which the surgeon determines ligating clips are the best choice. |
| Product code | FZP |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 24, 2017 |
| 510(k) numbers | K800079 |
| FEI number | 3005747797 |
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