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U.S. Department of Health and Human Services

Enforcement Report - Week of June 20, 2012

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Product Detail

Product Description Source Plasma
Recall Number B-1712-12
Classification Class II
Code Info Date range: 03/19/2008 - 07/20/2009 4080364443 4080363688 4080362157 4080360178 4080359825 4080357806 4080353533 4080350379 4080332278 4080330772 4080330031 4080322922 4080291696 4080289640 4080284174 4080282498 4080280450 4080272644 4080272049 4080266378 4080264124 4080263652 4080260090 4080247540 4080246828 4080245487 4080244786 4080243413 4080241829 4080241323 4080239819 4080239326 4080237977 4080237292 4080235880 4080235289 4080233975 4080233403 4080231973 4080231300 4080229657 4080229072
Product Distributed Qty 43 units
Reason For Recall Blood products, collected from a donor who did not have a complete physical examination, were distributed.

Event Detail

Event Id 54059
Product Type Biologics
Status Terminated
Recalling Firm CSL Plasma, Inc.
City Dayton
State OH
Country US
Voluntary / Mandated
Recall Initiation Date 2009-09-30
Initial Firm Notification of Consignee or Public E-Mail
Distribution Pattern IL, IN
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