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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K112652
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FDA Recall
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Philips SureSigns VSi / SureSigns VS2+ vital signs monitor used in healthcare environments and tran... 3 12/20/2017 Philips Electronics North America Corporation
Philips Healthcare SureSigns VS2+ Model 863278 SureSigns VS2+ NBP and SpO2 Model 863279 SureSigns ... 2 02/14/2013 Philips Healthcare Inc.
Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275, 863276, 863277... 2 08/30/2012 Philips Healthcare Inc.
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