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U.S. Department of Health and Human Services

Medical Device Recalls
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Recall Date to: 04/16/2014 PMA Number: P010025
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FDA Recall
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Selenia Full Field Digital Mammography System with software versions 5.0.x and 5.1.x The Selenia ... 2 09/30/2013 Hologic, Inc.
Selenia Full Field Digital Mammography System with Software v. 3.3.1.1; Full field digital, system, ... 3 05/28/2008 Lorad, A Hologic, Inc.
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