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U.S. Department of Health and Human Services

Enforcement Report - Week of December 5, 2012
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Product Detail

Product Description Source Plasma
Recall Number B-0090-13
Classification Class II
Code Info 07IMOD8365; 07IMOD8086; 07IMOD9626; 08IMOC2350; 08IMOC1236; 08IMOC0517; 08IMOB9411; 08IMOA7165; 07IMOF2982; 07IMOF1494; 07IMOE8541; 07IMOE8131; 07IMOE7029; 07IMOE5551; 07IMOE4790; 07IMOE2580; 07IMOE1607; 07IMOD9837; 07IMOD2723; 07IMOD3620; 07IMOD4070; 07IMOD5186; 07IMOD5575; 07IMOD6637; 07IMOD6938
Product Distributed Qty 25 units
Reason For Recall Blood products, collected from a donor who did not have a complete physical examination, were distributed.

Event Detail

Event Id 49304
Product Type Biologics
Status Terminated
Recalling Firm BioLife Plasma Services L.P.
City Independence
State MO
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2008-06-25
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern CA
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