Device recall
Z-0403-2010: Sterile Sheath, product code SS01.
FDA device recall · Class II · Surgical Devices/Covidien
Key facts
| Recall number (Z-number) | Z-0403-2010 |
|---|---|
| Recall event | 53694 |
| Product | Sterile Sheath, product code SS01. |
| Product code | GDW |
| Recalling firm | Surgical Devices/Covidien |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 8, 2010 |
| FEI number | 1219930 |
At a glance
- None Linked 510(k)s
- 10–99 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