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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
PMA Number: P990066
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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GE SENOGRAPHE 2000D FULL FIELD DIGITAL MAMMOGRAPHY SYSTEM ( SENO 2000D). The Senographe 2000D sys... 2 02/20/2012 GE Healthcare, LLC
GE SENOGRAPHE ESSENTIAL FULL FIELD MAMMOGRAPHY SYSTEM (SENO ESSENTIAL). The Senographe Essential ... 2 10/26/2011 GE Healthcare, LLC
GE SENOGRAPHE DS FULL FIELD DIGITAL ESSENTIAL MAMMOGRAPHY SYSTEM. The Senographe DS system genera... 2 10/26/2011 GE Healthcare, LLC
Seneographe 2000D Digital Mammography X-Ray System 2 07/20/2004 General Electric Med Systems
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