Device recall
Z-2313-2008: The St. Jude Medical Livewire TC" Ablation Catheter, 8mm Tip w/Thermocouple &…
FDA device recall · Class II · St. Jude Medical Cardiovascular Division
Key facts
| Recall number (Z-number) | Z-2313-2008 |
|---|---|
| Recall event | 48740 |
| Product | The St. Jude Medical Livewire TC" Ablation Catheter, 8mm Tip w/Thermocouple & Thermistor REF 402196, Length 115 cm, Lot 2056960, Manufacturer St. Jude Medical 14901 DeVeau Place, Minnetonka, MN 55345-2126 USA, Sterile EO The St. Jude Medical Livewire TC" Ablation Catheter is a flexible electrode… |
| Product code | LPB |
| Recalling firm | St. Jude Medical Cardiovascular Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 4, 2012 |
| PMA numbers | P960016 |
| FEI number | 2182269 |
At a glance
- None 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