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U.S. Department of Health and Human Services

Enforcement Report - Week of January 9, 2013

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Product Detail

Product Description Source Plasma
Recall Number B-0347-13
Classification Class II
Code Info 06FMOD0209
Product Distributed Qty 1 unit
Reason For Recall Blood product, identified as unsuitable due to a donor screening deviation, was distributed.

Event Detail

Event Id 45721
Product Type Biologics
Status Terminated
Recalling Firm BioLife Plasma Services L.P.
City Springfield
State MO
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2007-09-25
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern CA
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