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U.S. Department of Health and Human Services

Enforcement Report - Week of July 10, 2013

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Product Detail

Product Description Platelets Pheresis Leukocytes Reduced
Recall Number B-1657-13
Classification Class II
Code Info 4571232A; 4571232B; 4927022A; 4927022B; 4927021A; 4927021B.
Product Distributed Qty 6 units
Reason For Recall Blood Products, in which Antibody Screen Testing was performed incorrectly, were distributed.

Event Detail

Event Id 47926
Product Type Biologics
Status Terminated
Recalling Firm Northwest Florida Blood Center, Inc.
City Pensacola
State FL
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2008-01-16
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Distribution Pattern FL, AL
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