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U.S. Department of Health and Human Services

Enforcement Report - Week of July 25, 2012

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Product Detail

Product Description Source Plasma
Recall Number B-1621-12
Classification Class II
Code Info 08AOHB2829
Product Distributed Qty 1 unit
Reason For Recall Blood product, collected from a donor whose scheduled physical examination was incomplete, was distributed.

Event Detail

Event Id 50336
Product Type Biologics
Status Terminated
Recalling Firm BioLife Plasma Services L.P.
City Athens
State OH
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2008-10-29
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern CA
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