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Philips Respironics Recall

  • Philips has established a registration process that allows Patients, Users, or Caregivers to look up their device serial number and begin a claim if their unit is affected. At this time, this process is only available for Patients, Users, or Caregivers in the USA and Canada. More countries will be added shortly.


  • We want to make you aware of an important development related to certain CPAPs, BiPAPs, and ventilators manufactured by Philips Respironics. Please be sure to read this information in detail.


  • On June 14, 2021, Philips Respironics announced a voluntary recall for Continuous and Non-Continuous Ventilators (certain CPAP, BiPAP, and Ventilator Devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices. For information on the Recall Notice, a complete list of impacted products, and potential health risks, visit www.philips.com/src-update.


  • Medic Home Health Care is in communication with Philips about this recall and we will do our best to communicate information to out patients as it becomes available.


  • At this point, Philips has not provided the timing of the availability of potential future product replacement.


  • Please also reach out to your physician with any additional questions you may have regarding your therapy.



  • We realize this is unwelcome news, but please be assured that Medic Home Health Care's primary focus is on your health and safety.


  • If you have any questions please feel free to contact us online, by phone at (440) 449-7727, or visit our showroom at 760 Beta Dr, Suite A, Mayfield Village, OH 44143-2443.