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U.S. Department of Health and Human Services

Enforcement Report - Week of December 19, 2012

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Product Detail

Product Description Source Plasma
Recall Number B-0078-13
Classification Class II
Code Info 08OUTD6551, 08OUTD4301, 08OUTD3924, 08OUTD1660, 08OUTD1174, 08OUTD0586, 08OUTC5971, 08OUTC5400, 08OUTC4692, 08OUTC4317, 08OUTC3409, 08OUTC2970, 08OUTC2325, 08OUTC1695, 08OUTC1093, 08OUTC0373, 08OUTB9920, 08OUTB9060, 08OUTD5251, 08OUTD5616, , 08OUTD7075, 08OUTD7926, 08OUTD8806, 08OUTD9079, 08OUTE3717, 08OUTE4270, 08OUTE6072, 08OUTE8200, 08OUTE7490, 08OUTE6713, 08OUTE5972, 08OUTE5530, 08OUTE8484, 08OUTE5464, 08OUTE4979, 08OUTE3618, 08OUTE2621, 08OUTE2221, 08OUTE1511, 08OUTE0774, 08OUTE0325, 07OUTE6189, 07OUTE5921, 07OUTE5428, 07OUTE4998, 07OUTE4173, 07OUTE3749, 07OUTE2920, 07OUTE2343, 07OUTE7637,
Product Distributed Qty 50 units
Reason For Recall Blood products, collected from donors, whose suitability to donate was not adequately determined, were distributed.

Event Detail

Event Id 50285
Product Type Biologics
Status Terminated
Recalling Firm BioLife Plasma Services L.P.
City Layton
State UT
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2008-10-31
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern CA