Device recall
Z-0412-2007: Thoratec Dual Drive Console a drive component of the Thoratec Ventricular Assist…
FDA device recall · Class II · Thoratec Corp
Key facts
| Recall number (Z-number) | Z-0412-2007 |
|---|---|
| Recall event | 36154 |
| Product | Thoratec Dual Drive Console a drive component of the Thoratec Ventricular Assist Device, Model Numbers, 10025-2600-005, 10025-2601-007, 10025-2602-006, Thoratec Corporation, 6035 Stoneridge Drive, Pleasanton, CA 94588 |
| Product code | DSQ |
| Recalling firm | Thoratec Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 18, 2008 |
| PMA numbers | P870072 |
| FEI number | 2916596 |
At a glance
- None 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