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U.S. Department of Health and Human Services

Enforcement Report - Week of December 19, 2012

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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

Product Detail

Product Description Code Info Classification Reason for Recall Product Quantity Recall Number
Source Plasma 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, Class II Blood products, collected from donors, whose suitability to donate was not adequately determined, were distributed. 50 units B-0078-13
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