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U.S. Department of Health and Human Services

Enforcement Report - Week of May 1, 2013

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Product Detail

Product Description Source Plasma
Recall Number B-1304-13
Classification Class II
Code Info 5020156275, 5020157029, 5020157686, 5020158548, 5020159159, 5020160229, 5020160746, 5020161804, 5020162349, 5020162989, 5020164038, 5020164411, 5020165651, 5020165875, 5020167671, 5020171649, 5020172098, 5020172873, 5020173290, 5020174072, 5020174413, 5020175052, 5020175504, 5020176255, 5020176753, 5020177456, 5020178050
Product Distributed Qty 27 units
Reason For Recall Blood products, collected from a donor who was previously deferred, were distributed.

Event Detail

Event Id 59720
Product Type Biologics
Status Terminated
Recalling Firm Octapharma Plasma, Inc.
City Omaha
State NE
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2011-07-18
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern California
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