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U.S. Department of Health and Human Services

Enforcement Report - Week of June 19, 2013

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Product Detail

Product Description Fresh Frozen Plasma
Recall Number B-1583-13
Classification Class II
Code Info W1657120266156, W165712026601I, W165712026599B, W165712024396S, W165712024395U, W165712024393Y, W1657120243903, W165712024368*, W1657120243671, W1657120243655, W1657120243647, W1657120250687, W165712024819E, W165712023827U, W165712027716H, W165712027712P, W165712027704P, W165712027700X, W1657120214666, W1657120213053, W165712021364I, W165712020867P, W165712019069A, W165712000939F, W165712019313Y, W165712018284C, W1657120182151, W165712018196C, W165712018100N, W165712018099E, W165712018097I, W1657120101824, W165712015088V, W165712016583M, W1657120149183, W165712007005W, W165712006336A, W165712006225O, W165712013834R, W165712013658R, W165712010491F, W165712010967C, W165712010925W, W165711028973L, W165712010427V, W1657120104240, W165712008629Q, W165712007439H, W165712006880*, W165712005346I, W165712005429G, W165712004663C, W1657120046101, W165712004483K, W165712004307F, W1657120023997, W1657120023989, W165712002389B, W165712002383N, W165712002376L, W165712000189M, W1657120213205, W1657120195793, W165712022369T, W1657120189617, W165712025372S, W165712000927N, W1657120009008, W165712018308S, W1657120182868, W165712018171U, W165712018106B, W1657120106401, W165712010637B, W165712010563F, W1657120099697, W1657120099140, W165712009810G, W165712018318Q, W165712016555U, W165712007447H, W165712007446J, W165712007008Q, W165712007007S, W165712006981Q, W165712006963U, W1657120132181, W165712011854E, W165712006093G, W165712010960Q, W165712009948H, W1657120102616, W165712009811E, W1657120098340, W1657120100960, W1657120100864, W165712010243A, W165712010177Z, W1657120101664, W165712008483U, W165712008705Y, W165712007432V, W165712007391H, W1657120061938, W165712002380T, W165712013501W, W165712024191H, W1657120146114, W165712016584K, W165712018007H, W1657120182876, W165712016589A
Product Distributed Qty 112 units
Reason For Recall Blood products, collected from a potentially ineligible donor, were distributed.

Event Detail

Event Id 64176
Product Type Biologics
Status Terminated
Recalling Firm Our Lady Of The Lake Hospital Inc
City Baton Rouge
State LA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-12-21
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern 5 in Louisiana