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U.S. Department of Health and Human Services

Enforcement Report - Week of October 30, 2013

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Product Detail

Product Description Source Plasma
Recall Number B-2539-13
Classification Class II
Code Info 41500410323; 41500406367; 41500361365; 41500358115; 41500693300; 41500388963; 41500312432; 41500297930; 41500284769; 41500280653; 41500379899; 41500376284; 41500240900; 41500236326; 41500232070; 41500213506; 41500201433; 41500156302; 41500143085; 41500139916; 41500127245; 41500151472; 41500107990; 41500097816; 41500095140; 41500190279; 41500178190; 41500289375; 41500260193; 41500304660; 41500252214; 41500396330; 41500373606; 41500230550; 41500221354; 41500213282; 41500204335; 41500146729; 41500115252; 41500109127; 41500101395; 41500196970; 41500196267; 41500110144; 41500089445; 41500082374; 41500080424; 41500191837
Product Distributed Qty 48 Units
Reason For Recall Blood products, collected from a donor whose scheduled physical examination was incomplete, were distributed.

Event Detail

Event Id 60297
Product Type Biologics
Status Terminated
Recalling Firm Csl Plasma Inc
City Wichita
State KS
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2011-08-18
Initial Firm Notification of Consignee or Public E-Mail
Distribution Pattern Switzerland, Germany, IL, MA, CA
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