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U.S. Department of Health and Human Services

Enforcement Report - Week of October 17, 2012
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Event Detail

Event ID 51349
Product Type Biologics
Status Terminated
Recalling Firm CSL Plasma, Inc
City Charlotte
State NC
Country US
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date 2009-01-09
Initial Firm Notification of
Consignee or Public		 Other
Distribution Pattern IL & Switzerland

Product Detail

Product Description Code Info Classification Reason for Recall Product Quantity Recall Number
Source Plasma 4180357508, 4180356223, 4180355586, 4180354295, 4180353710, 4180352509, 4180351968, 4180350287, 4180349041, 4180348511, 4180347274, 4180345499, 4180344657, 4180343823, 4180343000, 4180341053, 4180340360, 4180337642, 4180336133, 4180335468, 4180334421, 4180333841, 4180332742, 4180332015, 4180330994, 4180330361, 4180328295, 4180326367, 4180324587, 4180318627, 4180317614, 4180316239, 4180315098, 4180313340, 4180311686, 4180309998, 4180307699, 4180306098, 4180304902, 4180304275, 4180303246, 4180299690, 4180299081, 4180296193, 4180295467, 4180294037, 4180293389, 4180292056 Class II Blood products, collected from a donor whose routine physical examination was inadequately documented, were distributed. 48 units B-2157-12
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