We apologize for the inconvenience this has caused you and will do our best to keep you fully informed as more information is available.
Philips recall serial number#
Philips will be handling all machine replacements and has created a registration process that allows you to look up your device serial number and begin a claim if the unit is affected.Ĭlick here to see if your PAP device has been impacted. Philips is also advising patients who continue to use their machines that they should manually clean them due to the fact that the health risks related to this recall may be exacerbated by using ozone-based cleaning methods.ĪdaptHealth and its affiliates are following Philips’ recall guidance. For any patients with severe OSA or other chronic health conditions, we strongly recommend discussing any change in therapy with your physician prior to a change.
Philips recall update#
Read FAQs about the recall posted by the FDA.Important Update from AdaptHealth about the Philips RecallĪt AdaptHealth, your health and safety are our biggest priority.Īs you know, Philips recently issued a recall for 3-4 million CPAP machines and ventilators due to potential long-term health consequences of the foam used to dampen the machine’s sound.Īt this time, Philips is advising patients to stop using their devices at this time and contact their healthcare provider for next steps. Philips has issued supplemental clinical information on the risks to patients posed by the devices affected by the product defect in sound abatement form.Your provider also may discuss other treatment options with you. Your provider may prescribe a new PAP device for you. A polyurethane foam component designed to keep the machines quietly running can break down into small.
due to a part that may be degrading into a toxic carcinogen. Your medical provider can help you determine if you should continue or discontinue treatment. Between three and four million Philips brand assisted breathing devices are being voluntarily recalled in the U.S.
Philips recall how to#
View a video about how to register your Philips SRC medical device.Use the Philips registration process to look up your device serial number.Visit the Philips recall webpage for current information.What should you do if you use a Philips PAP device? In September 2021, Philips estimated that the process will take one year to complete. Philips has begun a process to repair and replace affected devices. Philips has received no complaints related to chemical exposure. To date, there have been no reports of death. Philips reports that in 2020 the complaint rate for foam particles was low (0.03%). Exposure to VOCs may cause problems such as: Testing results suggest these emissions taper off during the initial days of use of a new device. These “volatile organic compounds” are released as gases. Testing by Philips also found that the foam can produce unsafe chemical levels. Philips reports that the potential risks to you include: As a result, you may inhale the particles when using the device. These particles can enter the humidifier, tubing and mask. Over time, the foam inside the machine may fall apart into black particles. The recall is related to the type of foam used to reduce the noise made by the devices. Most of the recalled devices are first-generation DreamStation products. These include CPAP and BPAP devices to treat obstructive sleep apnea. On June 14, Philips issued a voluntary recall for specific Philips Respironics devices. Resources for Health Care Professionals.