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Durable Medical Equipment (DME)

Important Notice on DME Recall

On June 14th, 2021 the FDA announced that certain models of CPAP, BiPAP and ventilators from Philips Respironics were being recalled.  Philips is instructing any patient using an affected CPAP or BiPAP device, to discontinue use of the affected units and talk to your doctor.  Philips is instructing patients using an affected life-sustaining ventilator to continue treatment until they are able to discuss treatment options with their physician.