Device recall
Z-0007-2014: Bard LifeStent Solo Vascular Stent, Item Numbers: EX062001CL, EX072001CL…
FDA device recall · Class I · Bard Peripheral Vascular Inc
Key facts
| Recall number (Z-number) | Z-0007-2014 |
|---|---|
| Recall event | 66374 |
| Product | Bard LifeStent Solo Vascular Stent, Item Numbers: EX062001CL, EX072001CL, EX062003CL, EX072003CL. The LifeStent Solo Vascular Stent System is intended to improve luminal diameter in the treatment of symptomatic de-novo or restenotic lesions up to 240 mm in length in the native superficial femoral… |
| Product code | NIP |
| Recalling firm | Bard Peripheral Vascular Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Feb 5, 2014 |
| PMA numbers | P070014, P070014S032 |
| FEI number | 2020394 |
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