Device recall
Z-0015-2007: Thoratec brand Sealed Arterial Cannula for use with the Thoratec Vascular Assist…
FDA device recall · Class II · Thoratec Corp
Key facts
| Recall number (Z-number) | Z-0015-2007 |
|---|---|
| Recall event | 36138 |
| Product | Thoratec brand Sealed Arterial Cannula for use with the Thoratec Vascular Assist Device System, Model Number(s): Catalogue numbers: #100118-- Short, 14mm graft; #100121-- Long, 14mm graft; #100129-- Long, 18mm graft. Manufactured by Thoratec Corporation, 6035 Stoneridge Drive, Pleasanton, CA 94588 |
| Product code | DSQ |
| Recalling firm | Thoratec Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 27, 2007 |
| PMA numbers | P870072, P920014 |
| 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