High heat and high humidity environments as well as unapproved cleaning methods such as ozone, may also contribute to foam degradation. Per Philips Respironics, possible health risks include exposure to degraded sound abatement foam and exposure to chemical emissions from the foam material. The foam degradation may be exacerbated by use of unapproved cleaning methods, such as ozone, and high heat and high humidity environments may also contribute to foam degradation.” What Is the Safety Hazard Associated With This Issue? Philips Respironics identified there is risk the PE-SUR sound abatement foam “may degrade into particles which may enter the device’s air pathway and be ingested or inhaled by the user, and the foam may off-gas certain chemicals. We are absolutely committed to supporting the worldwide community of patients who rely on our Sleep & Respiratory Care solutions for their health and quality of life, and the physicians and customers who are dedicated to meeting patient needs.” Why Did Philips Respironics Issue a Voluntary CPAP Recall?
This effort includes wide-scale, global ramping up of manufacturing, repair, services, supply chain and other functions to support the correction. Our intention is to give affected patients and customers the service they expect and deserve as we resolve this matter as our top priority.
“We cannot stress enough that Philips is treating this matter with the highest possible seriousness, and are dedicating significant time and resources to address this issue. Per the Philips Respironics recall notice: Per Philips Respironics CEO Frans van Houten “We deeply regret any concern and inconvenience that patients using the affected devices will experience because of the proactive measures we are announcing today to ensure patient safety.” On Monday, June 14th, Philips Respironics issued a voluntary recall on nearly all of their CPAP, APAP, and BiPAP machines sold from 2009 until today, with some exceptions.
Philips cpap machines recall update#
As information becomes available, we will update our customers via email and the CPAP community at large using this blog. Not all details of this recall are known at this time. We will continue to take any actions Philips Respironics or the organizations governing them approve relating to this recall as quickly as we are able to execute them.īelow is the information you need to know on this recall, how you might be impacted, what next steps should be taken, and what you should expect.
We have completed all requests by Philips Respironics and we eagerly await a plan that will allow us to provide actionable solutions to customers.
Philips cpap machines recall full#
We learned of this recall at the same time as our customers and have been in daily communication with Philips Respironics since that time.ĭespite sincere and full efforts by members of the Philips Respironics team we’ve been in contact with, details and actions we can take immediately to have a positive impact on the health of our customers have been in short supply. All of the relationships we hold dear, our family, friends, coworkers, and customers are affected. Since the news broke, customers have let us know they are frustrated and concerned. was recently notified by Philips Respironics of a recall for certain CPAP, APAP, and BiPAP devices.
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