Device recall
Z-2450-2012: Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of…
FDA device recall · Class II · Abbott Vascular
Key facts
| Recall number (Z-number) | Z-2450-2012 |
|---|---|
| Recall event | 63092 |
| Product | Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of lesions in the vasculature. |
| Product code | LIT |
| Recalling firm | Abbott Vascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 15, 2013 |
| 510(k) numbers | K111899 |
| FEI number | 2024168 |
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