Device recall
Z-0933-2007: St. Jude Medical-CPS Direct SL- slittable CRT lead delivery tool. -Model Numbers…
FDA device recall · Class II · St Jude Medical CRMD
Key facts
| Recall number (Z-number) | Z-0933-2007 |
|---|---|
| Recall event | 37818 |
| Product | St. Jude Medical-CPS Direct SL- slittable CRT lead delivery tool. -Model Numbers 410110, 410111, 410112, 410113, 410114, 410115, 410116, 410120,410121. 410122, 410123, 410124, 410125 and 410126. |
| Product code | MCX |
| Recalling firm | St Jude Medical CRMD |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 29, 2012 |
| 510(k) numbers | K053277 |
| FEI number | 2017865 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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