Device recall
Z-2327-2026: CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930
FDA device recall · Class II · INSPIREMD Inc
Key facts
| Recall number (Z-number) | Z-2327-2026 |
|---|---|
| Recall event | 98922 |
| Product | CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930 |
| Product code | NIM |
| Recalling firm | INSPIREMD Inc |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P240029 |
| FEI number | 3032814119 |
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