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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K090483
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FDA Recall
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Philips SureSigns VM1SpO2, C02, Rec, model no. 863266 - Product Usage: The SureSigns VM1 is a patien... 2 06/10/2020 Philips North America, LLC
Philips SureSigns VS2 monitor, 863079 863080 863081 863082 863283 863286 The Sure Signs VS2... 2 08/22/2018 Philips Electronics North America Corporation
Philips SureSigns VS3 Vital Signs Monitor Models: VS3 863069, 863070, 453564041251, 453564041261, ... 2 06/17/2011 Philips Healthcare Inc.
SureSigns Patient Monitors (VM3, VM4. VM6. VM8): VM3 3/5 lead ECG/SPo2, Respiration Bedside P... 2 11/23/2009 Philips Healthcare Inc.
SureSigns Vital Signs Viewer (VSV):Spot Check Vital Signs Monitor with NBP (options to include Predi... 2 11/23/2009 Philips Healthcare Inc.
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