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U.S. Department of Health and Human Services

Enforcement Report - Week of September 12, 2012

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Product Detail

Product Description Fresh Frozen Plasma
Recall Number B-2177-12
Classification Class II
Code Info 003KT21845, 003KT22093, 003KT21844, 003KT21846, 003KP40859, 003KT22248, 003KF32591, 003KT23823, 003KF30043, 003KJ21806, 003KJ21790, 003KP40848, 003KP40870, 003KF30502, 003KJ21312, 003KJ21314, 003KT23926, 003KJ21345, 003KJ21727, 003KJ21729, 003KT21947, 003KT21814, 003KP40853, 003KJ21368, 003KJ21372, 003KT23988, 003KT24059, 003KT24152, 003KT24159, 003KP47200, 003KT24275, 003KT24288, 003KT24318, 003KJ21821, 003KP40829, 003KP40832, 003KP40858, 003KT24112, 003KT21927, 003KT23932, 003KT23928, 003KT23941, 003KT24281, 003KT21808, 003KT21831, 003KT21931, 003KP40866, 003KP40872, 003KF30085, 003KT22261, 003KT22262, 003KF32600, 003KQ40068, 003KT23894, 003KT23897, 003KT23940, 003KT23945, 003KP46744, 003KP46750, 003KJ21375, 003KJ21395, 003KJ21435, 003KQ40330, 003KT24018, 003KT24021, 003KT24114, 003KT24116, 003KT24145, 003KT24269, 003KT24286, 003KT24302, 003KF30497, 003KF30500, 003KF30530, 003KT22122, 003KT22128, 003KT22135, 003KT24171, 003KT24247, 003KT21200, 003KT21201, 003KT21204, 003KT24291, 003KT21821, 003KT21843, 003KP40837, 003KP40862, 003KP40871, 003KF3000, 003KF30139, 003KT22110, 003KF30504, 003KT22132, 003KT22133, 003KT22136, 003KT23831, 003KJ21351, 003KJ21392, 003KJ21427, 003KJ21436, 003KT23991, 003KT24051, 003KJ21699, 003KT24283, 003KT24301, 003KT24311, 003KT24315, 003KJ21804, 003KJ21850, 003KT21836, 003KT21842, 003KP40840, 003KT21981, 003KF30007, 003KF30073, 003KF30197, 003KT22131, 003KT22134, 003KT24118, 003KT21938, 003KJ21782, 003KT21849, 003KQ40059, 003KT21834, 003KQ40067, 003KJ21616, 003KJ21859, 003KJ21861, 003KT24014, 003KT21820, 003KT21824, 003KT21825, 003KT21827, 003KT21830, 003KT21837, 003KT21840, 003KP40838, 003KP40839, 003KF30037, 003KT21839, 003KF30040, 003KF30048, 003KF30056, 003KT22079, 003KT22082, 003KF30517, 003KT22259, 003KQ40066, 003KT23929, 003KT23933, 003KT23949, 003KT23954, 003KT23955, 003KJ21361, 003KJ21362, 003KJ21394, 003KJ21397, 003KT23970, 003KT24007, 003KT24199, 003KJ21774, 003KJ21784, 003KJ21785, 003KT24274, 003KT24330, 003KJ21839, 003KJ21852, 003KF30512, 003KT24327, 003KP40863, 003KF30057, 003KT22080, 003KT22081, 003KT22084, 003KT22255, 003KJ21305, 003KT24015, 003KT24300, 003KT22292, 003KT23636, 003KT23757, 003KT24011, 003KT22083, 003KT21810, 003KT24148, 003KJ21843, 003KJ21846, 003KT21203, 003KT21209, 003KT21813, 003KP40857, 003KF30097, 003KT22111, 003KF30507, 003KF30515, 003KT22119, 003KT23925, 003KJ21428, 003KT24077, 003KT24113, 003KJ21717, 003KJ21730, 003KP47192, 003KP47196, 003KP47197, 003KP47199, 003KJ21796, 003KJ21880, 003KT24047, 003KT21206, 003KT21848, 003KP40827, 003KP40835, 003KP40852, 003KP40855, 003KF30011, 003KF30016, 003KF30025, 003KF30091, 003KF32594, 003KF32604, 003KF32615, 003KQ40062, 003KT23836, 003KT24047, 003KJ21863, 003KT21816, 003KT21818, 003KT23805, 003KT23819, 003KJ21348, 003KT24246, 003KT23811, 003KT24312, 003KJ21313, 003KT21972, 003KT22093, 003KJ21449, 003KT21940, 003KT21970, 003KJ21308, 003KJ21697, 003KP46746, 003KT23636, 003KT23816, 003KT24251, 003KF30027, 003KF30090, 003KT21847, 003KP40868, 003KF30046, 003KT22123, 003KF30513, 003KT24255, 003KP47191, 003KP47193, 003KF30020, 003KT22197, 003KT22239, 003KT24057, 003KT24065, 003KP47188, 003KP47203, 003KT22253, 003KT24074, 003KT24074, 003KT22243, 003KT24063, 003KT23838, 003KT24048, 003KT24266, 003KJ21878, 003KF30104, 003KJ21315, 003KT22249
Product Distributed Qty 275 units
Reason For Recall Blood products, collected from a donor in which donor suitability was not adequately determined, were distributed.

Event Detail

Event Id 44996
Product Type Biologics
Status Terminated
Recalling Firm The American National Red Cross - Southern Region
City Douglasville
State GA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2007-09-25
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern AL, GA & SC