Device recall
Z-0159-2009: WECK Hem-o-lok Non-absorbable Polymer Ligation Clips, Rx Only, Sterile, Teleflex…
FDA device recall · Class II · Telefelx Medical
Key facts
| Recall number (Z-number) | Z-0159-2009 |
|---|---|
| Recall event | 49452 |
| Product | WECK Hem-o-lok Non-absorbable Polymer Ligation Clips, Rx Only, Sterile, Teleflex Medical, RTC, NC 27709. The use of the reusable Teleflex Medical metal ligating clips is transient, invasive and intended for the application of hemostatic clips during general open surgery. Ligation clips are… |
| Product code | FZP |
| Recalling firm | Telefelx Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 15, 2012 |
| 510(k) numbers | K021808 |
| 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