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U.S. Department of Health and Human Services

Enforcement Report - Week of March 13, 2013

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Product Detail

Product Description Source Plasma
Recall Number B-0220-13
Classification Class III
Code Info 0530052514, 0530052215, 0530050895, 0530050580, 0530047198, 0530046819, 0530046556, 0530046177, 0530045908, 0530045575, 0530045209, 0530044864, 0530044645, 0530044165, 0530043843, 0530043544, 0530043221, 0530042952, 0530042614, 0530042283, 0530041970, 0530041692, 0530041301, 0530040953, 0530040591, 0530040201, 0530040019, 0530039491, 0530039298, 0530038835, 0530038580, 0530038196, 0530037947, 0530037640, 0530037395, 0530037079, 0530036854, 0530036272, 0530035763, 0530035112, 0530034619, 0530034010, 0530033447, 0530031462, 0530031138, 0530030785, 0530030640, 0530030316, 0530029897, 0530029726, 0530029139, 0530028900, 0530028569, 0530028132, 0530024940, 0530024718, 0530024335, 0530024098, 0530023670, 0530023432, 0530023031.
Product Distributed Qty 61 units
Reason For Recall Blood products, collected from a donor who was previously deferred, were distributed.

Event Detail

Event Id 48953
Product Type Biologics
Status Terminated
Recalling Firm Biomat USA, Inc.
City Portland
State OR
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2008-03-17
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Spain and California
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