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U.S. Department of Health and Human Services

Enforcement Report - Week of October 3, 2012

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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

Product Detail

Product Description Code Info Classification Reason for Recall Product Quantity Recall Number
Source Plasma 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 Class II Blood products, collected from a donor whose scheduled physical examination was incomplete, were distributed. 53 units B-2336-12
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