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U.S. Department of Health and Human Services

Enforcement Report - Week of August 14, 2013

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Product Detail

Product Description Plasma Frozen within 24 hours
Recall Number B-1886-13
Classification Class II
Code Info W045110218862; W045110218228; W045110219150; W045110219133; W045110210656; W045111228041; W045111229352; W045111229346; W045111229357; W045111225190; W045111231079; W045111233272; W045111232665; W045110218231; W045110200646; W045110218881; W045110218871; W045110213441; W045111224033; W045111225176; W045111233944; W045111232672; W045111233256; W045110200597; W045110210605; W045111228038; W045111232153; W045111243753; W045111234996; W045111234965; W045110218220; W045110219117; W045110220269; W045110220275; W045110218888; W045110210954; W045110213390; W045110213380; W045110213399; W045111232147; W045111232146; W045111231101; W045111233997; W045111233034; W045111233048; W045111243759; W045111243767; W045110218217; W045110218885; W045110210950; W045110216721; W045110222097; W045110222102; W045111231077; W045111231132; W045111233774; W045111233277; W045111232692; W045111233253; W045111240428; W045110219137; W045110218884; W045110218893; W045110213393; W045110210615; W045110210666; W045110218970; W045111227286; W045110198849; W045110202805; W045110198475; W045110198484; W045110203117; W045110203137; W045110209903; W045110209834; W045110203727; W045110214447; W045110200142; W045110198483; W045110199767; W045110198364; W045110209301; W045110208591; W045110208631; W045110209864; W045110213775; W045110198504; W045110208572; W045110208563; W045110198834; W045110198859; W045110198513; W045110198614; W045110198713; W045110198639; W045110198637; W045110198711; W045110202815; W045110198473; W045110203604; W045110211604; W045110211608; W045110203730; W045110211930; W045110214470; W045110198595; W045110198517; W045110202813; W045110205954; W045110203039; W045110199181; W045110208558; W045110203664; W045110213145; W045110213174; W045110213140; W045110198293; W045110199773; W045110198567; W045110198553; W045110198381;W045110198369; W045110198451; W045110205970; W045110205886; W045110211917; W045110203746; W045110193495; W045110211938
Product Distributed Qty 130 Units
Reason For Recall Blood products, collected in a manner that may have compromised the sterility of the collection system, were distributed.

Event Detail

Event Id 59132
Product Type Biologics
Status Terminated
Recalling Firm Community Blood Center of the Ozarks
City Springfield
State MO
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2011-04-18
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern MO; TX; AR; NC; TN; OH; MS;
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