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U.S. Department of Health and Human Services

Enforcement Report - Week of October 17, 2012

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Product Detail

Product Description Source Plasma
Recall Number B-2615-12
Classification Class II
Code Info 06IMOA7790; 06IMOA7228; 06IMOA6898; 06IMOA6322; 06IMOA6048
Product Distributed Qty 5 units
Reason For Recall Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.

Event Detail

Event Id 42262
Product Type Biologics
Status Terminated
Recalling Firm BioLife Plasma Services LP
City Independence
State MO
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2006-05-15
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern IL