Device recall
Z-0337-2011: RX ACCULINK Carotid Stent System 9 X 20mm, Part Number: 1011341-20, Lot Number…
FDA device recall · Class II · Abbott Vascular
Key facts
| Recall number (Z-number) | Z-0337-2011 |
|---|---|
| Recall event | 56973 |
| Product | RX ACCULINK Carotid Stent System 9 X 20mm, Part Number: 1011341-20, Lot Number: 0071361 The RX Acculink Carotid Stent System, used in conjunction with Abbott Vascular RX Accunet embolic protection system, is indicated for the treatment of patients at high risk for adverse events from carotid… |
| Product code | NIM |
| Recalling firm | Abbott Vascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 16, 2010 |
| PMA numbers | P040012 |
| FEI number | 2024168 |
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