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U.S. Department of Health and Human Services

Enforcement Report - Week of May 1, 2013

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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

Product Detail

Product Description Code Info Classification Reason for Recall Product Quantity Recall Number
Source Plasma 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 Class II Blood products, collected from a donor who was previously deferred, were distributed. 27 units B-1304-13
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