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U.S. Department of Health and Human Services

Enforcement Report - Week of December 19, 2012

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Event Detail

Event ID 54971
Product Type Biologics
Status Terminated
Recalling Firm CSL Plasma, Inc.
City Kansas City
State MO
Country US
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date 2009-11-25
Initial Firm Notification of
Consignee or Public
Other
Distribution Pattern Illinois; Germany; Switzerland

Product Detail

Product Description Code Info Classification Reason for Recall Product Quantity Recall Number
Source Plasma 4100277850; 4100276582; 4100275333; 4100274081; 4100272722; 4100271544; 4100269970; 4100268693; 4100267245; 4100265930; 4100264695; 4100263580; 4100262073; 4100260749; 4100259294; 4100258041; 4100256558; 4100254300; 4100253637; 4100243130; 4100241888; 4100240692; 4100239324; 4100238183; 4100236832; 4100235771; 4100234597; 4100232998; 4100232190; 4100230520; 4100229264; 4100228088; 4100226938; 4100225617; 4100224715; 4100223221; 4100221952; 4100221045; 4100219439; 4100215576; 4100214281; 4100213246; 4100211933; 4100211056; 4100209898; 4100208871; 4100207555; 4100206958; 4100205556; 4100204906. Class II Blood products, collected from a donor whose scheduled physical examination was incomplete, were distributed. 50 Units B-0149-13
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