Integra LifeSciences Corp. (NeuroSciences) recalls Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550
- Recalling company
- Integra LifeSciences Corp. (NeuroSciences)
- 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 the catheter's bullet shaped tip.
- Reason
- Out-of-specification endotoxin result that did not meet the acceptance criteria.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 10, 2026
- Reported
- May 20, 2026
- Distribution
- US Nationwide distribution in the states of Arizona (AZ), Arkansas (AR), California (CA), Connecticut (CT), Florida (FL), Kentucky (KY), Louisiana (LA), Michigan (MI), Minnesota (MN), Missouri (MO), North Carolina (NC), North Dakota (ND), Oklahoma (OK), Oregon (OR), Texas (TX), Washington (WA).
- Status
- Ongoing
- Quantity
- 40 packs (200 units)
- Lot / codes
- Product ID: 37.550.501. UDI-DI: 10381780530138. Lot Number: 45322.
- Company location
- Princeton, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2173-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2173-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.