Device recall
Z-2108-2017: WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-2108-2017 |
|---|---|
| Recall event | 77102 |
| Product | WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin closure of lacerations on the outer layer of the dermis for a wide range of general, thoracic, obstetric, gynecological, orthopedic, cardiovascular, urological, and plastic… |
| Product code | GDT |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Completed |
| 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