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U.S. Department of Health and Human Services

Enforcement Report - Week of December 19, 2012
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Product Detail

Product Description Source Plasma
Recall Number B-0148-13
Classification Class II
Code Info 4210323584; 4210304150; 4210303303; 4210297992; 4210293731; 4210291514; 4210289430; 4210288836; 4210285683; 4210283789; 4210281923; 4210279978; 4210279178; 4210276807; 4210271979; 4210271352; 4210263791; 4210262764; 4210259138; 4210256999; 4210255306; 4210254855; 4210252067; 4210250138; 4210248709; 4210247652; 4210245956; 4210244829; 4210243609; 4210242768; 4210228374; 4210227747; 4210225801; 4210224285; 4210222290; 4210220217; 4210218485; 4210217989; 4210216569; 4210215918; 4210214293; 4210209079; 4210208585.
Product Distributed Qty 43 Units
Reason For Recall Blood products, collected from a donor whose scheduled physical examination was incomplete, were distributed..

Event Detail

Event Id 54050
Product Type Biologics
Status Terminated
Recalling Firm CSL Plasma, Inc.
City Omaha
State NE
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2009-09-22
Initial Firm Notification of Consignee or Public Other
Distribution Pattern Illinois; Germany; Switzerland
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