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U.S. Department of Health and Human Services

Medical Device Recalls

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Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-1972-2021 - Philips Respironics E30 with Humidifier, Continuous Ventilator, Minimum Ventilatory Support, Facility Use; Product Numbers DSX9999H11, INX9999H19, RINX9999H19 The Philips Respironics E30 ventilato... 1 07/13/2021 Philips Respironics, Inc.
Z-1974-2021 - SystemOne (Q-Series), DreamStation, DreamStation Go, Dorma 400, Dorma 500, REMstar SE Auto Noncontinuous Ventilators The Philips Respironics E30 ventilator is intended to provide invasive and non-... 1 07/13/2021 Philips Respironics, Inc.
Z-1973-2021 - DreamStation ASV, DreamStation ST, AVAPS, SystemOne ASV4, C-Series ASV, C-Series S/T and AVAPS, OmniLab Advanced+ Continuous Ventilator, Non-life Supporting The Philips Respironics E30 ventilator i... 1 07/13/2021 Philips Respironics, Inc.
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