Notice names this product. Integra LifeSciences (NeuroSciences)’s Codman CerebroFlo EVD Catheter with Endexo Technology is named in FDA Class II recall Z-2173-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Out-of-specification endotoxin result that did not meet the acceptance criteria. Identifying details: Product ID: 37.550.501. UDI-DI: 10381780530138. Lot Number: 45322.. Units affected: 40 packs (200 units). Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
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.
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
Out-of-specification endotoxin result that did not meet the acceptance criteria.
Company / brand: Integra LifeSciences (NeuroSciences) recalls
Affected product: Codman CerebroFlo EVD Catheter with Endexo Technology recall status
Official ID Z-2173-2026 · Official record ↗
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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.