Device recall
Z-0946-2009: Epicor LP Connecting Cable, CC-6-LP-CE, Catalog Number 12263, an accessory to…
FDA device recall · Class II · St. Jude Medical Inc
Key facts
| Recall number (Z-number) | Z-0946-2009 |
|---|---|
| Recall event | 50521 |
| Product | Epicor LP Connecting Cable, CC-6-LP-CE, Catalog Number 12263, an accessory to the Epicor Cardiac Ablation Control System, manufactured by St.Jude Medical, Sunnyvale, CA Disposable connecting cable, accessory to the Epicor Cardiac Ablation Control System. The cable is used to connect the Epicor… |
| Product code | OCL |
| Recalling firm | St. Jude Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 28, 2010 |
| 510(k) numbers | K080292 |
| FEI number | 2938836 |
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