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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 Source Plasma
Recall Number B-2370-12
Classification Class III
Code Info 380001943, 380002525, 380004157, 380005454, 380006271, 380007553, 380007713, 380002110. 380001521, 380003365, 380003625, 380005713, 380006093, 380008037, 380008629, 380008896, 380009446, 380009942, 380010141, 380010432, 380010668, 380011122, 380011476, 380012030, 380012185, 380012470, 380012689, 380013021, 380013200, 380013643, 380013915, 380014838, 380015927, 380016011, 380016486.
Product Distributed Qty 35 units
Reason For Recall Blood products, collected from a donor, whose suitability to donate was not adequately determined, were distributed

Event Detail

Event Id 39858
Product Type Biologics
Status Terminated
Recalling Firm Biomat USA, Inc.
City Los Angeles
State CA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2005-03-08
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern all units were shipped to Spain
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