Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.

FDA has issued a Class I recall for a handful of Philips Respironics BiPAP ventilator devices following 13 reported injuries and eight deaths connected to the models. Impacted ventilator models ...

NOW has launched rtNOW Engage, a suite of turnkey service lines to support durable medical equipment (DME) companies, including follow-up checks for non-invasive ventilation (NIV) and BiPAP patients ...