Device recall
Z-0078-2013: Hem-o-lok Large Polymer Ligating Clips, REF #544240, Rx only, Sterile, Teleflex…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0078-2013 |
|---|---|
| Recall event | 63365 |
| Product | Hem-o-lok Large Polymer Ligating Clips, REF #544240, Rx only, Sterile, Teleflex Medical, Research Triangle Park, NC 27709. Teleflex Medicals Hem-o-lok polymer ligating clips are single use, sterile, non-absorbable medial devices that have been designed to ligate vessels and tissue structures during… |
| Product code | FZP |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 8, 2012 |
| 510(k) numbers | K993157 |
| 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