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U.S. Department of Health and Human Services

Enforcement Report - Week of May 1, 2013

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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

Product Detail

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