Device recall
Z-2253-2020: Multifire VersaTrack Auto Suture Hernia Stapler, 4.8mm, Part No. 174023…
FDA device recall · Class II · Covidien Llc
Key facts
| Recall number (Z-number) | Z-2253-2020 |
|---|---|
| Recall event | 85689 |
| Product | Multifire VersaTrack Auto Suture Hernia Stapler, 4.8mm, Part No. 174023 - Product Usage: has application in endoscopic general surgery procedures for fixation of mesh in the repair of hernial defects and in other surgical specialties for approximation of tissue(s). |
| Product code | GCI |
| Recalling firm | Covidien Llc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K912097 |
| FEI number | 1282497 |
At a glance
- 1–9 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