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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-0080-13
Classification Class II
Code Info 4100356139; 4100352050; 4100349660; 4100348615; 4100347189; 4100344881; 4100343098; 4100341929; 4100340798; 4100339619; 4100337254; 4100335779; 4100334476; 4100333203; 4100332004; 4100330362; 4100329365; 4100327908; 4100327047; 4100325518; 4100324794; 4100322468; 4100319907; 4100309110; 4100306283; 4100299035; 4100269941; 4100261168; 4100258592; 4100255865; 4100253193; 4100250678; 4100249217; 4100248010; 4100244455; 4100241666; 4100204861; 4100203016; 4100201527.
Product Distributed Qty 39 Units
Reason For Recall Blood products, collected from a donor whose scheduled physical examination was incomplete, were distributed.

Event Detail

Event Id 54210
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 2009-11-06
Initial Firm Notification of Consignee or Public Other
Distribution Pattern Illinois
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