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U.S. Department of Health and Human Services

Enforcement Report - Week of February 19, 2014

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Event Detail

Event ID 67068
Product Type Biologics
Status Ongoing
Recalling Firm Life Technologies Corporation
City Brown Deer
State WI
Country US
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date 2013-11-22
Initial Firm Notification of
Consignee or Public
Letter
Distribution Pattern Nationwide; NETHERLANDS, GREECE, RUSSIA, INDIA, SOUTH AFRICA, FRANCE, GERMANY, ITALY, TURKEY, UNITED KINGDOM, DUBAI, IRELAND, SWITZERLAND, NEW ZEALAND, SWEDEN, SPAIN, INDONESIA, SAUDI ARABIA, JAPAN, URUGUAY, CHINA, TAIWAN.

Product Detail

Product Description Code Info Classification Reason for Recall Product Quantity Recall Number
Invitrogen by Life Technologies: DRB1-15 SSP UniTray® Kit, 450102D; DRB1-15 SSP UniTray® Kit with Taq Polymerase, 450112D; AllSet+" Gold SSP HLA DRB1-15/16 High Res Kit, 54290D. 450102D: 010743202, 0111049955, 0111274159, 011872999 450112D 010743202807163, 010743202824730, 010743202847129, 010743202867121, 010743202904081, 01110499551314672, 01110499551273533, 01112741591345434, 01112741591377037, 011872999934454, 011872999943913, 011872999952219, 0118729991029899 54290D: 001769069, 001796673, 0021103796, 0021216660, 0021344999, 002905389, 002979632 Class II HLA typing assay, associated with false negative results, were distributed. 3 kits B-0284-14
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