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U.S. Department of Health and Human Services

Enforcement Report - Week of May 1, 2013

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Product Detail

Product Description Source Plasma
Recall Number B-1305-13
Classification Class II
Code Info 08MMTA9682, 08MMTB0851, 08MMTB1337, 08MMTB2193, 08MMTB2754, 08MMTB4201, 08MMTB4806, 08MMTB5684, 08MMTB7612, 08MMTC5407, 08MMTD4599, 08MMTD5282, 08MMTD7218, 08MMTD7759, 08MMTD8524, 08MMTD9118, 08MMTE0004, 08MMTE0530, 08MMTE1679, 08MMTE2222, 08MMTE3113, 08MMTE3639, 08MMTE4431, 08MMTE5000, 08MMTE5803, 08MMTE6341, 08MMTE8054, 08MMTE9039, 08MMTG0340, 08MMTG2052, 08MMTG2674, 08MMTG4548, 08MMTG5251, 08MMTG6972, 08MMTG9432, 08MMTH1559, 08MMTH2210, 08MMTH3307, 08MMTH4516, 08MMTH5036, 08MMTH6212, 08MMTC3877, 08MMTC6269, 08MMTC6741, 08MMTC7565, 08MMTC8055, 08MMTC8805, 08MMTC9297, 08MMTD0410, 08MMTD1409, 08MMTD1948, 08MMTE7732
Product Distributed Qty 52 units
Reason For Recall Blood products, collected from a donor whose record was incomplete, were distributed.

Event Detail

Event Id 52267
Product Type Biologics
Status Terminated
Recalling Firm BioLife Plasma Services L.P.
City Missoula
State MT
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2009-04-13
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern California, Austria