Drug recall
Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo…
FDA recall event 98752 · Class II · Integra LifeSciences Corp. (NeuroSciences)
Key facts
| Event ID | 98752 |
|---|---|
| Recall numbers | Z-2173-2026 |
| Recalling firm | Integra LifeSciences Corp. (NeuroSciences) |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Out-of-specification endotoxin result that did not meet the acceptance criteria. |
| Initiation date | Apr 10, 2026 |
| Report date | May 20, 2026 |
| City | Princeton |
| State | NJ |
| Country | United States |
| FEI number | 3003418325 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: