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U.S. Department of Health and Human Services

Enforcement Report - Week of July 24, 2013

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Event Detail

Event ID 50444
Product Type Biologics
Status Terminated
Recalling Firm Csl Plasma Inc
City Tempe
State AZ
Country US
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date 2008-10-07
Initial Firm Notification of
Consignee or Public
Letter
Distribution Pattern Illinois, Switzerland, Germany

Product Detail

Product Description Code Info Classification Reason for Recall Product Quantity Recall Number
Source Plasma 4270183014, 4270181851, 4270180003, 4270174788, 4270173161, 4270171887, 4270165471, 4270162492, 4270161125, 4270160357, 4270159126, 4270157892, 4270157329, 4270155736, 4270155211, 4270153782, 4270153425, 4270152091, 4270151567, 4270150167, 4270148507, 4270147032, 4270146491, 4270145367, 4270144221, 4270143653, 4270141052, 4270139728, 4270139214, 4270138216, 4270137713, 4270136676, 4270136156, 4270134929, 4270134542, 4270131147, 4270129852 Class II Blood products, collected from a donor who did not have a complete physical examination, were distributed. 37 units B-1629-13
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