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U.S. Department of Health and Human Services

Enforcement Report - Week of September 25, 2013

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Product Detail

Product Description Source Plasma
Recall Number B-2296-13
Classification Class II
Code Info 07CIAM3734, 07CIAM3038, 07CIAM2132
Product Distributed Qty 3 units
Reason For Recall Blood products, collected from a donor with a history of hepatitis and fatty liver disease, were distributed.

Event Detail

Event Id 48373
Product Type Biologics
Status Terminated
Recalling Firm BioLife Plasma Services L.P.
City Cedar Rapids
State IA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2008-04-29
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern Austria
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