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U.S. Department of Health and Human Services

Enforcement Report - Week of August 8, 2012
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Product Detail

Product Description Cryoprecipitated AHF
Recall Number B-1778-12
Classification Class II
Code Info 4503210, 4507505, 4512262, 4512867, 4514814, 4515182, 4515587, 4518110, 4519381, 4521445, 4524695, 4526651, 4527024, 4527375, 4527402, 4527793, 4528427, 4528621, 4528674, 4528756, 4528771, 4529623, 4529759, 4530146, 4530660, 4531509, 4533447, 4533528, 4533547, 4534603, 4535112, 4536300, 4536584, 4536744, 4538230, 4538258, 4538687, 4539147, 4540392, 4540707, 4540746, 4541404, 4541841, 5515497, 5516643, 5516647, 5517146, 5517324, 5519447, 5520083, 5523075, 5523087, 5523111, 5523319, 5523379, 5524079, 5526510, 5528942, 5529724, 5531070, 6501366, 6501857, 6503167, 6504576, 4507936, 4512975, 5512343
Product Distributed Qty 67
Reason For Recall Blood products, collected from donors whose confirmatory syphilis testing was invalid, were distributed.

Event Detail

Event Id 42130
Product Type Biologics
Status Terminated
Recalling Firm Northern California Community Blood Bank
City Eureka
State CA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2006-04-17
Initial Firm Notification of Consignee or Public Telephone
Distribution Pattern CA, NJ, OH, TN
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