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U.S. Department of Health and Human Services

Enforcement Report - Week of October 17, 2012
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Product Detail

Product Description Source Plasma/Liquid Plasma
Recall Number B-2169-12
Classification Class II
Code Info 4240203191; 4240202188; 4240201501; 4240200163; 4240199668; 4240198041; 4240196915; 4240196219; 4240195380; 4240194609; 4240193795; 4240193268; 4240192176; 4240191692; 4240190721; 4240190268; 4240189306; 4240189065; 4240188195; 4240187586; 4240186387; 4240185611; 4240184951; 4240183873; 4240183517; 4240182263; 4240181724; 4240180641; 4240180206; 4240179162; 4240178951; 4240177911; 4240177729; 4240176805; 4240176099; 4240175018; 4240174624; 4240173554; 4240172999; 4240172073; 4240171396; 4240170548; 4240169885; 4240168756; 4240168208; 4240167150; 4240166625; 4240165560; 4240165043; 4240164097; 4240163516; 4240162425; 4240161746; 4240160819
Product Distributed Qty 54 units
Reason For Recall Blood products, collected from a donor whose physical examination was incomplete, were distributed.

Event Detail

Event Id 48850
Product Type Biologics
Status Terminated
Recalling Firm Csl Plasma Inc
City Boca Raton
State FL
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2008-05-20
Initial Firm Notification of Consignee or Public E-Mail
Distribution Pattern Illinois, Switzerland, Germany
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