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U.S. Department of Health and Human Services

Enforcement Report - Week of December 5, 2012

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Event Detail

Event ID 55397
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 2010-01-12
Initial Firm Notification of
Consignee or Public
Other
Distribution Pattern Illinois; North Carolina; Germany; Switzerland

Product Detail

Product Description Code Info Classification Reason for Recall Product Quantity Recall Number
Source Plasma 0111149111; 0111147834; 0111146858; 0111145398; 0111144544; 0111140295; 0111139418; 0111137586; 0111136853; 0111135164; 0111132473; 0111110562; 0111108783; 0111108007; 0111105480; 0111104143; 0111103129; 0111101609; 0111100446; 0111098621; 0111097833; 0111096140; 0111094912; 0111093305; 0111092212; 0111090898; 0111089695; 0111086002; 0111084770; 0111083520; 0111082406; 0111081158; 0111079979; 0111078736; 8750013927; 8750012649; 8750011299; 8750009785; 8750008278; 8750007210; 8750005857; 8750003894; 8750000361; 0111072791; 0111070491; 0111069856; 0111066340; 0111065204; 0111062461; 0111061817; 0111057970; 0111056553; 0111053550; 0111052886. Class II Blood products, which were collected from a donor in which donor suitability were not adequately determined, were distributed 54 Units B-0093-13
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