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Catheter, Ventricular (Containing Antibiotic Or Antimicrobial Agents)

FDA product code NHC · Class 2 · Neurology

2
Registered devices
44
Adverse events
2
Recalls
3
510(k) clearances

Devices with this code

Recent 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-threaten
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 twi

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.