Reported May 20, 2026 · Ongoing

Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD…

Integra LifeSciences Corp. (NeuroSciences)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Integra LifeSciences Corp. (NeuroSciences) · 1100 Campus Rd · Princeton, NJ · 08540-6650

Is this the product you have?

  • Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets
  • Product ID37.550.501. 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
Lot codes and dates
  • Product ID37.550.501
  • UDI-DI10381780530138
  • Lot Number45322
Amount recalled
40 packs (200 units)

Where it was sold

Why it was recalled

Out-of-specification endotoxin result that did not meet the acceptance criteria.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 3:30 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.