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U.S. Department of Health and Human Services

Enforcement Report - Week of December 12, 2012

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Product Detail

Product Description Source Plasma
Recall Number B-0160-13
Classification Class III
Code Info TQ192038
Product Distributed Qty 1 unit
Reason For Recall Blood product, collected from a donor for whom donor suitability was not adequately determined, was distributed.

Event Detail

Event Id 63435
Product Type Biologics
Status Terminated
Recalling Firm Knoxville Plasma Corporation
City Knoxville
State TN
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-09-10
Initial Firm Notification of Consignee or Public E-Mail
Distribution Pattern California
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