Source: FDA | Recall date: 05/20/2026
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Affected 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
Summary: Out-of-specification endotoxin result that did not meet the acceptance criteria.
Hazard: Out-of-specification endotoxin result that did not meet the acceptance criteria.
Track your baby products and get automatic recall alerts when something may affect your family.
Learn more about the baby product recall tracker, baby product recall alerts, or recall monitoring plans.