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U.S. Department of Health and Human Services

Enforcement Report - Week of October 17, 2012

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Product Detail

Product Description Source Plasma
Recall Number B-1996-12
Classification Class II
Code Info 5080238043; 5080237145; 5080235642; 5080235128; 5080234049; 5080233479; 5080232406; 5080225818; 5080224961; 5080223129; 5080221982; 5080215743; 5080214633; 5080213587;
Product Distributed Qty 14
Reason For Recall Blood products, collected from a donor whose physical examination was incomplete, were distributed.

Event Detail

Event Id 62446
Product Type Biologics
Status Terminated
Recalling Firm Octapharma Plasma, Inc.
City Norfolk
State VA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-05-16
Initial Firm Notification of Consignee or Public E-Mail
Distribution Pattern Austria
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