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Ventriclear

COOK INCORPORATED · Model G32429 · UDI-DI 00827002324299

NHC Prescription
3
510(k) clearances
44
Adverse events (1 deaths)
2
Recalls
3
Facilities

Description

Ventriclear Ventricular Drainage Catheter Set with Cook Spectrum Antibiotic Impregnation

Recalls

DateFirmReason
2018-05-31Cook Inc.This lot of VentriClear failed endotoxin testing. Potential adverse events include immune responses ranging from non-specific febrile reaction to life-threatening systemic inflamm
2015-11-19Cook Inc.Cook Medical initiated a voluntary recall of specific lot numbers of the VentriClear II Ventricular Drainage Catheter Set due to the device being sterilized twice, which may result

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.