Phillips Respironics Recall Information
what you need to know
In June of 2021, Philips Respironics issued an official recall for certain ventilators, BiPAP, and CPAP machines due to potential health risks caused by the degradation of the polyester-based polyurethane foam used in these devices. This breakdown of materials can result in serious injury which can be life-threatening, cause permanent impairment, or require medical intervention.
OxyMed understands how important it is for our patients to have access to the most accurate, up-to-date information regarding product recalls. Find links below for all the most current and relevant Philips recall information. If you have questions or concerns, please do not hesitate to reach out to our team or call us at (205) 981-2333