{"url_path":"/fda/device/recalls/Z-2173-2026","section_key":"summary","section_title":"DEVICE Recall: Integra LifeSciences Corp. (NeuroSciences) — 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.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-10","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2173-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Integra LifeSciences Corp. (NeuroSciences)"},"word_count":145,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2173-2026\n\n**Recalling firm:** Integra LifeSciences Corp. (NeuroSciences)\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-10\n**Report date:** 2026-05-20\n\n## Product\nCodman 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.\n\n## Reason\nOut-of-specification endotoxin result that did not meet the acceptance criteria.\n\n## Affected lots\nProduct ID: 37.550.501. UDI-DI: 10381780530138. Lot Number: 45322.\n\n## Distribution\nUS 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)."}