Device recall
Z-0406-2010: Intelligent Delivery System, Straight, product code iDriveS; Intelligent…
FDA device recall · Class II · Surgical Devices/Covidien
Key facts
| Recall number (Z-number) | Z-0406-2010 |
|---|---|
| Recall event | 53694 |
| Product | Intelligent Delivery System, Straight, product code iDriveS; Intelligent Delivery System, Curved, product code iDriveC; Intelligent Delivery System, Flexible, product code iDriveF. |
| Product code | GDW |
| Recalling firm | Surgical Devices/Covidien |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 8, 2010 |
| 510(k) numbers | K073001 |
| FEI number | 1219930 |
At a glance
- 1–9 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