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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-0771-13
Classification Class III
Code Info 5020185308, 5020177821, 5020176494, 5020175673, 5020175310, 5020173228, 5020172653, 5020171774, 5020170189, 5020170018, 5020168215, 5020167663, 5020164608, 5020164282, 5020158730, 5020158015, 5020152164, 5020151620, 5020147950, 5020140986, 5020140595, 5020137968
Product Distributed Qty 22 units
Reason For Recall Blood products, collected from a donor for whom donor suitability was not adequately determined, were distributed.

Event Detail

Event Id 59507
Product Type Biologics
Status Terminated
Recalling Firm Octapharma Plasma Inc
City Omaha
State NE
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2011-07-28
Initial Firm Notification of Consignee or Public E-Mail
Distribution Pattern California
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