Device recall
Z-0491-03: Thoratec Sterile LVAD Pneumatic Lead 5''; Model/Product Number: 20010-0000-108
FDA device recall · Class III · Thoratec Corp
Key facts
| Recall number (Z-number) | Z-0491-03 |
|---|---|
| Recall event | 25262 |
| Product | Thoratec Sterile LVAD Pneumatic Lead 5'' ; Model/Product Number: 20010-0000-108 |
| Product code | DSQ |
| Recalling firm | Thoratec Corp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 21, 2003 |
| PMA numbers | P870072, P870072S012 |
| 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