Device recall
Z-2538-2016: Weck EFx Classic Fascial Closure System, Rx Only, Sterile, The product is…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-2538-2016 |
|---|---|
| Recall event | 74683 |
| Product | Weck EFx Classic Fascial Closure System, Rx Only, Sterile, The product is intended to facilitate placement and withdrawal of suture loops to repair port side defects following laparoscopic surgery |
| Product code | HCF |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 25, 2020 |
| 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