Device recall
Z-2911-2026: Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with…
FDA device recall · Class II · Contego Medical, Inc
Key facts
| Recall number (Z-number) | Z-2911-2026 |
|---|---|
| Recall event | 99353 |
| Product | Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP System), REF: NG-0630-140-2, NG-0640-140-2, NG-0730-140-2, NG-0740-140-2, NG-NV-6-30, NG-NV-6-40, NG-NV-7-30, NG-NV-7-40 |
| Product code | NIM |
| Recalling firm | Contego Medical, Inc |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P240009 |
| FEI number | 3011471056 |
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