CAREFUSION 2420-0500

Adverse Event reported on 1/25/2013

Device Attributes
AttributeValue
ManufacturerCAREFUSION
Brand NameCAREFUSION
Device TypeINFUSION SET
Product CodeFPA
Model Number2420-0500
Catalog Number2420-0500
Device Operator0HP
CAREFUSION CAREFUSION INFUSION SET   Back to Search Results
Model Number 2420-0500
Event Date 01/20/2013
Event Type  Malfunction  
Event Description

Secondary i. V. Fluid noticeably by passed the in-line check valve and entered the drip chamber as well as the primary i. V. Fluid bag.

 
Source: FDA