Device recall
Z-0640-2012: LigaSure V 5 mm Dolphin Tip Laparoscopic 37 cm Sealer/Divider, LS1500, Sterile…
FDA device recall · Class II · Covidien, PLC
Key facts
| Recall number (Z-number) | Z-0640-2012 |
|---|---|
| Recall event | 60462 |
| Product | LigaSure V 5 mm Dolphin Tip Laparoscopic 37 cm Sealer/Divider, LS1500, Sterile EO, Manufactured for Valleylab, a division of Tyco Healthcare Group LP, Boulder, CO. Manufactured by Covidien Medical Products (Shanghai) Manufacturing LLC, Building No. 10, 789 Puxing Road, Shanghai 201114, P.R. Chin… |
| Product code | GEI |
| Recalling firm | Covidien, PLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 22, 2013 |
| 510(k) numbers | K031011 |
| FEI number | 1717344 |
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