Device recall
Z-2173-2026: Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product…
FDA device recall · Class II · Integra LifeSciences Corp. (NeuroSciences)
Key facts
| Recall number (Z-number) | Z-2173-2026 |
|---|---|
| Recall event | 98752 |
| Product | Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD Catheter is a 3.3 mm diameter (10 Fr.), 35 cm long polyurethane catheter for diverting cerebrospinal fluid (CSF) from the ventricles of the brain through a series of drainage holes near… |
| Product code | JXG |
| Recalling firm | Integra LifeSciences Corp. (NeuroSciences) |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K170599 |
| FEI number | 3003418325 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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