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U.S. Department of Health and Human Services

Enforcement Report - Week of July 24, 2013

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Product Detail

Product Description Source Plasma
Recall Number B-1701-13
Classification Class III
Code Info 5250051627, 5250051321, 5250050643, 5250050422, 5250049708, 5250049571, 5250048584, 5250047966, 5250047708, 5250046985, 5250046641, 5250046068, 5250045742, 5250045161, 5250044825, 5250044144, 5250043890, 5250042937, 5250041894, 5250041609, 5250040334, 5250040089, 5250038529
Product Distributed Qty 23 units
Reason For Recall Source Plasma, collected from donors who did not have a complete medical history interview, was distributed.

Event Detail

Event Id 59509
Product Type Biologics
Status Terminated
Recalling Firm Octapharma Plasma, Inc.
City Charlotte
State NC
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2011-07-01
Initial Firm Notification of Consignee or Public E-Mail
Distribution Pattern Austria
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