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U.S. Department of Health and Human Services

Enforcement Report - Week of August 29, 2012

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Product Detail

Product Description Source Plasma
Recall Number B-1287-12
Classification Class II
Code Info 380017145, 380016941, 380016754, 380016610, 380016394, 380016226, 380015934, 380015846, 380015692, 380015570, 380015308, 380015112, 380014344, 380013925, 380013756, 380013475, 380013131, 380012882, 380012613, 380012361, 380012134, 380011958, 380011604, 380011323, 380010943, 380010817, 380010306, 380010299, 380009793, 380009785, 380009266, 380008811, 380008710, 380008281, 380008184, 380007743, 380007677, 380007001, 380006596, 380006435, 380006007, 380005874, 380005430, 380005279, 380004898, 380004255, 380003648, 380003044, 380002818
Product Distributed Qty 49 units
Reason For Recall Blood products, collected from a donor who was previously deferred, were distributed.

Event Detail

Event Id 40693
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 2005-08-16
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Spain
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