Device recall
Z-0759-2017: Weck Facial Closure Systems have application in laparoscopic procedures for…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0759-2017 |
|---|---|
| Recall event | 75693 |
| Product | Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing incision sites. |
| Product code | HCF |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2017 |
| 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