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U.S. Department of Health and Human Services

Enforcement Report - Week of October 3, 2012

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Product Detail

Product Description Source Plasma
Recall Number B-2336-12
Classification Class II
Code Info 7020569758;7020569243;7020561213;7020560515;7020559510;7020558871;7020557589;7020556923;7020555960;7020554644;7020554249;7020551927;7020549396;7020548750;7020546254;7020545607;7020543963;7020542709;7020541769;7020541080;7020540134;7020537340;7020536579;7020535741;7020534950;7020533777;7020532633;7020531792;7020530859;7020530108;7020528828;7020528109;7020527346;7020526610;7020525530;7020525122;7020522123;7020521031;7020518895;7020518020;7020516872;7020516410;7020514961;7020514002;7020505987;7020504543;7020501835;7020501348;7020500269;7020499825;7020496782;7020496011;7020495192
Product Distributed Qty 53 units
Reason For Recall Blood products, collected from a donor whose scheduled physical examination was incomplete, were distributed.

Event Detail

Event Id 38672
Product Type Biologics
Status Terminated
Recalling Firm ZLB Bioplasma, Inc.
City Aurora
State CO
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2007-04-20
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern IL, IN, Germany, Switzerland
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