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.

Class II

Recalling firm: Integra LifeSciences Corp. (NeuroSciences)
Reason for recall: Out-of-specification endotoxin result that did not meet the acceptance criteria.
Affected products (lot / model / serial): Product ID: 37.550.501. UDI-DI: 10381780530138. Lot Number: 45322.
Units affected: 40 packs (200 units)
Distribution pattern: 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).
Firm location: Princeton, NJ, United States
Recall type: Voluntary: Firm initiated
How the firm notified customers: Letter
Product type: Devices
Status: Ongoing
Recall number: Z-2173-2026
Recall initiated: April 10, 2026
FDA classification date: May 13, 2026
FDA report date: May 20, 2026
FDA event ID: 98752
Last updated on HTM Vibe: July 24, 2026