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U.S. Department of Health and Human Services

Enforcement Report - Week of August 7, 2013

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Product Detail

Product Description Source Plasma
Recall Number B-1972-13
Classification Class II
Code Info 4080319226 4080318753 4080316469 4080313795 4080300331 4080297687 4080258643 4080251284 4080250193 4080249518 4080247964 4080247099 4080245763 4080245107 4080243103 4080242441 4080240908 4080240294 4080238911 4080236960 4080235535 4080234863 4080233687 4080232326 4080231293 4080229645 4080228565 4080226946 4080225852 4080225233 4080223440 4080222876
Product Distributed Qty 32 units
Reason For Recall Blood products, collected from a donor whose physical was improperly documented, were distributed.

Event Detail

Event Id 52146
Product Type Biologics
Status Terminated
Recalling Firm ZLB Bioplasma, Inc.
City Dayton
State OH
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2009-02-28
Initial Firm Notification of Consignee or Public E-Mail
Distribution Pattern IL, Germany.
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