Device recall
Z-3224-2017: Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments is…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-3224-2017 |
|---|---|
| Recall event | 77974 |
| Product | Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips to soft tissue during laparoscopic… |
| Product code | GEI |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 6, 2020 |
| 510(k) numbers | K153063 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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