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U.S. Department of Health and Human Services

Enforcement Report - Week of May 1, 2013

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Product Detail

Product Description Source Plasma
Recall Number B-1349-13
Classification Class II
Code Info 4170096945, 4170096061, 4170085861, 4170085417
Product Distributed Qty 4 units
Reason For Recall Blood products, collected from a donor who did not have a complete physical examination, were distributed.

Event Detail

Event Id 45071
Product Type Biologics
Status Terminated
Recalling Firm ZLB Bioplasma, Inc.
City Tulsa
State OK
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2009-11-30
Initial Firm Notification of Consignee or Public Other
Distribution Pattern IL, Switzerland
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