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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
Recall Date to: 10/31/2014 PMA Number: P010025
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Product Description
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FDA Recall
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Hologic Selenia Full Field Digital Mammography System: SEL-00002, SEL-00013, SEL-00030, SEL-00039. ... 2 06/03/2014 Hologic, Inc.
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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