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U.S. Department of Health and Human Services

Enforcement Report - Week of September 26, 2012
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Product Detail

Product Description Source Plasma
Recall Number B-2214-12
Classification Class II
Code Info 4100392051, 4100391500, 4100389118, 4100388452, 4100387385, 4100386645, 4100385652, 4100384768, 4100382850, 4100382474, 4100380926, 4100380407, 4100378762, 4100378159, 4100376439, 4100375784, 4100373987, 4100373333, 4100371396, 4100370969, 4100369129, 4100368322, 4100366367, 4100365648, 4100363580, 4100362777, 4100360899, 4100360181, 4100358258, 4100357376, 4100355646, 4100354819, 4100352727, 4100351938, 4100350267, 4100349445, 4100347445, 4100346605, 4100344801, 4100343970, 4100342162, 4100341325, 4100339782, 4100339283, 4100337032, 4100336269, 4100334446, 4100333691, 4100332065, 4100331442
Product Distributed Qty 50 units
Reason For Recall Blood products, collected from a donor who did not have a complete physical examination, were distributed.

Event Detail

Event Id 54209
Product Type Biologics
Status Terminated
Recalling Firm Csl Plasma Inc
City Boca Raton
State FL
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2009-11-09
Initial Firm Notification of Consignee or Public Other
Distribution Pattern IL
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