Device recall
Z-1472-2013: Versaport Bladeless Optical Fixation Cannula - 5mm Product Code: ONBFCA5ST The…
FDA device recall · Class II · Covidien LP
Key facts
| Recall number (Z-number) | Z-1472-2013 |
|---|---|
| Recall event | 65093 |
| Product | Versaport Bladeless Optical Fixation Cannula - 5mm Product Code: ONBFCA5ST The Versaport" Bladeless Optical 5mm trocars are intended for use in a variety of gynecologic, general, thoracic and urologic endoscopic procedures to create and maintain a port of entry. |
| Product code | GCJ |
| Recalling firm | Covidien LP |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 12, 2014 |
| 510(k) numbers | K112349 |
| FEI number | 1219930 |
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