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In Canada, the topic of CPAP machine recalls has remained at the forefront of sleep health conversations since the original Philips recall shook the market in 2021. Fast-forward to 2023–2025, and Canadians continue to navigate a complicated recall environment, especially if they use equipment from major brands like Philips or ResMed. But what exactly has happened in the last few years, and where do Canadian users stand now?
Let’s break it down clearly — starting with what was recalled, why it was recalled, and how Health Canada responded. For reference, you can review official recall information via Health Canada’s Recalls and Safety Alerts and the U.S. FDA Medical Device Recall Database.
The Philips CPAP recall started in 2021, but updates through 2023–2025 have significantly altered the scope and severity of the issue in Canada.
The primary concern involves the degradation of PE-PUR sound abatement foam, which can disintegrate and release:
These materials may enter the airway and cause a range of symptoms, from headaches and cough to more severe respiratory or even carcinogenic concerns.
Unlike Philips, ResMed has not issued a formal product recall in Canada between 2023 and 2025. However, it’s important to note that:
Despite the lower profile of these issues, it has led many users to become more cautious — especially given the growing scrutiny of respiratory equipment.
Canadian regulators have taken a stronger stance since 2023.
Health Canada:
For Canadians, this means greater transparency — but also a heightened need to remain informed about what’s happening.
Amid this climate of recalls and uncertainty, Canadian users are increasingly exploring BeC CPAP Machines as a safer, locally trusted alternative.
Here’s why:
Why does this matter? Because while many Canadians are waiting months for replacement devices from Philips, BeC CPAP offers fast delivery and support, backed by a Canadian team.
If you’re concerned about your Philips or ResMed device — or simply ready to switch — BeC CPAP Machines provide a proven, cost-effective, and recall-free option for continued sleep apnea therapy. Just call +1 (855) 860-3404
The landscape of CPAP machine recalls is still evolving. Philips is still managing the fallout from earlier recalls, and while ResMed remains more stable, some Canadian users have lost confidence.
What’s the safest move? Stay informed. Register your device. Check recall notices often. And if you’re tired of waiting or worried about your current unit, consider BeC CPAP for uninterrupted, trusted therapy — right here in Canada.
Next: We’ll explore which specific Philips and ResMed models are under recall and what Canadian users should know about checking their machines.
In a climate of uncertainty surrounding CPAP recalls, Canadian patients are searching for alternatives they can trust. While global brands like Philips and ResMed have dominated the market for years, the ongoing recall concerns — especially those tied to foam degradation and chemical exposure — have opened the door for safer, locally focused solutions. Enter BeC CPAP Machines: a Canadian alternative that has never been subject to a product recall and is rapidly becoming the go-to option for patients across Ontario and the rest of Canada.
Let’s be honest: CPAP therapy is not optional for people living with sleep apnea. It’s a medical necessity. That’s why reliability and safety must come first. The Philips recall alone, first issued in 2021 and continuing with updates into 2025, has impacted over 15 million devices globally, including hundreds of thousands distributed across Canada.
The core issue? PE-PUR sound foam degradation, which can release potentially carcinogenic particles and gases into the patient’s airway.
Even ResMed, though not formally recalled in Canada, has issued field safety notices about device performance issues, including internal valve degradation. The message is clear: patients deserve better.
That’s where BeC CPAP Machines stand apart.
Unlike global manufacturers whose recall strategies are managed out of the U.S. or Europe, BeC CPAP is a Canadian-first company. The devices are developed and distributed with full compliance to Health Canada guidelines.
That means:
When you’re dealing with a sleep disorder, the last thing you want is to question the safety of your equipment. BeC’s track record makes it an increasingly appealing option for Canadian households.
Many patients are surprised at how much value BeC offers, especially compared to bigger-name competitors.
Each BeC CPAP machine comes:
Whether you live in Toronto, Ottawa, Vancouver, or Halifax, BeC CPAP machines are available for quick order through Beccpap.ca, with bilingual support and expert follow-up.
“We switched to BeC after my Philips machine was recalled. The transition was smooth, and the difference in air quality is noticeable.” — Anna L., Mississauga, ON
BeC isn’t just a great option for individual users — it’s also gaining traction in Canadian clinics. With ongoing shortages of replacement parts for Philips and long service queues for ResMed, BeC is quickly becoming the preferred partner for home testing programs and rental units.
BeC partners enjoy:
Sleep professionals now recommend BeC CPAP as a first-line option for patients newly diagnosed with sleep apnea — not just as a recall backup.
Some common reasons people are switching from Philips and ResMed to BeC include:
In uncertain times, certainty matters. BeC provides that certainty.
For too long, Canadian patients have relied on global CPAP brands that, while advanced, have shown vulnerabilities in safety and accountability. As more information surfaces about the long-term effects of inhaling foam particles or experiencing system failures, users are rightly re-evaluating their options.
BeC CPAP Machines offer a clean slate — recall-free, patient-focused, and built for Canadians. Calendly button
If you’re using a CPAP machine in Canada, especially from Philips or ResMed, it’s critical to know whether your device has been affected by a recall. Since the Philips recall first began in 2021, the list of impacted models has grown significantly, extending into 2025. While ResMed machines have not seen the same level of action, certain advisory notices have sparked concern among patients and clinicians alike.
This section offers a detailed, Canada-focused list of currently recalled or flagged CPAP, BiPAP, and ventilator machines from Philips and ResMed, alongside their status with Health Canada and manufacturer recommendations.
As of 2025, Philips continues to manage one of the largest medical device recalls in history. The core issue remains the breakdown of PE-PUR foam, which can degrade and release harmful particles and gases into the user’s airway.
Here’s a breakdown of Philips machines currently under recall in Canada, based on Health Canada and FDA databases:
Philips has clarified that the following are not currently included in the recall:
Still, it’s best to check your serial number on the official Philips Recall Portal to be sure.
As of 2025, ResMed has not issued any formal CPAP recalls in Canada. However, that doesn’t mean all is quiet:
Canadian users can use the following resources:
If you’re unsure or experience any symptoms like headaches, coughing, or dizziness while using your CPAP, consult your sleep specialist immediately.
If your Philips device is on the recall list:
Or, if you’re done waiting — consider a recall-free CPAP machine like those from BeC CPAP. All units are compliant with Canadian safety regulations and include mask, tubing, and filters.
Book a call with CPAP Expert right now
Since the Philips CPAP recall began in 2021 and extended into 2025, thousands of users across Canada have reported a wide range of health symptoms linked to their use of affected devices. The recall was specifically issued due to the potential breakdown of the PE-PUR sound abatement foam, which can degrade over time and release harmful particles and chemical gases into the air pathway.
In this section, we’ll explore the reported symptoms, Health Canada’s findings, and what Canadian CPAP users need to monitor if they’ve used or are still using a recalled Philips device.
PE-PUR (polyester-based polyurethane) foam was used in many Philips devices to reduce noise. However, under conditions of high heat and humidity, the foam can degrade.
This degradation can lead to:
According to Health Canada’s classification, this poses both immediate and long-term health risks, including respiratory irritation and potential carcinogenic effects.
Many Canadian patients who used recalled Philips CPAP machines have reported symptoms that emerged within days or weeks of regular use:
These symptoms often overlap with those of untreated sleep apnea, making it difficult for some users to immediately identify the device as the cause.
“I thought I was just adjusting to my new mask, but the sore throat and coughing kept getting worse. It wasn’t until I read about the recall that I realized my DreamStation was part of it.” — James K., Calgary
Health Canada and the U.S. FDA have flagged more serious risks with long-term exposure to degraded foam particles and gases. These include:
Although direct causation has not been universally confirmed, animal studies cited by Philips and reviewed by the FDA show toxic effects in lung tissue with chronic exposure to PE-PUR degradation by-products.
Several Canadian sleep clinics, including in Ontario, British Columbia, and Alberta, have reported clusters of patients presenting with these symptoms. Some clinics have urged patients to discontinue use of affected devices where alternatives like BeC CPAP Machines are available.
In a 2023 internal study by a Toronto-based sleep centre, 18% of patients using recalled Philips units reported persistent respiratory symptoms that improved once they switched devices.
If you suspect your CPAP machine may be contributing to your symptoms:
Many users ignored early symptoms, attributing them to allergies or dry winter air. But growing evidence in Canada points to a direct connection between degraded foam exposure and respiratory or neurological symptoms.
If something feels off — pay attention. Your device might be doing more harm than good.
Next: We’ll look specifically at whether ResMed CPAP machines are part of any current recall or advisory notice in Canada.
As of 2025, ResMed CPAP machines are not subject to any formal recalls in Canada. Unlike Philips, which has faced an ongoing recall crisis due to degrading PE-PUR foam, ResMed has maintained a stable safety record — at least officially. However, that doesn’t mean ResMed devices have been entirely without concern.
This section takes a clear, Canada-focused look at the status of ResMed machines, what notices have been issued, and what Canadian users should know.
Note: No formal recalls have been issued by ResMed or mandated by Health Canada as of November 2025.
That said, in 2023, ResMed issued a field safety notice for a subset of its widely used AirSense 10 CPAP machines, warning about:
These were not linked to chemical exposure or foam breakdown like in the Philips case. Still, Health Canada monitored the situation and published a notice in its database under product advisories.
Though none are formally recalled, the following models have been mentioned in various manufacturer communications or field notices:
Health Canada has not issued any Class I, II, or III recall designations for these units.
You can check ResMed advisories through your CPAP supplier or the ResMed Canada website.
Although there is no widespread medical device recall, some Canadian patients have reported:
It’s worth noting that these reports are often tied to machine age or lack of maintenance, rather than a systemic safety failure.
“My AirSense 10 started delivering uneven pressure after four years of use. It turned out to be the internal valve, which my clinic replaced quickly.” — Derek M., Ottawa
In short: Not at this time, according to Health Canada.
However, the 2023 field safety notice demonstrated that even trusted brands must continuously monitor performance. ResMed has committed to regular firmware updates and device checks, especially for older AirSense 10 units distributed before 2020.
If you’re unsure about your unit:
If you’re looking for an option with zero recall history and strong Canadian support, consider switching to a BeC CPAP Machine:
While ResMed continues to be considered safe, it’s essential for patients to stay updated. Even in the absence of recalls, field safety notices and patient reports serve as important reminders to monitor your machine’s performance and know your alternatives.
Next, we’ll explain how to check if your CPAP machine has been recalled, whether it’s from Philips, ResMed, or another brand.
If you’re using a CPAP, BiPAP, or ventilator machine in Canada and you’re unsure whether it’s affected by a recall, you’re not alone. With high-profile recalls — particularly those involving Philips Respironics devices — many Canadians are left wondering if their equipment is still safe.
This section provides a step-by-step guide tailored to Canadian users to help determine if your CPAP machine has been recalled, and what actions to take next.
Before you can check recall status, you’ll need to gather the following information from your device:
Take note of any production or manufacturing dates on the label as well. These details are often required to verify recall eligibility.
Visit the official Philips Recall Portal.
Here, you can:
Use the Health Canada Recalls and Safety Alerts Database:
This resource allows you to:
If you’re unsure about your device’s status, your local supplier or sleep clinic is often the fastest way to verify:
CTA: For example, clinics working with BeC CPAP often help patients confirm their device’s status and offer a safe, immediate replacement if needed.
Even if your machine isn’t officially recalled, stay alert for signs of malfunction or chemical exposure:
If you notice any of these issues, consult your sleep specialist and stop using the device only if they advise it.
As of 2025, ResMed machines have not been formally recalled in Canada. However, users should:
Here’s what to do if your device is listed as recalled:
BeC CPAP units are available across Canada with masks, tubing, and filters included, and are often more affordable than recalled brands.
Knowing whether your CPAP machine is under recall could protect your health and help you avoid long-term risks. Thankfully, with proper tools and support, Canadian users can take control of the situation quickly.
Next: We’ll look at the latest update from the FDA and Philips about the ongoing CPAP recall situation.
As of 2025, the ongoing CPAP recall involving Philips Respironics has reached a new phase, with important developments issued by both the U.S. Food and Drug Administration (FDA) and Philips itself. While the original recall dates back to June 2021, recent actions and findings continue to impact Canadian patients, especially those still using affected models.
In this section, we break down the most recent updates from both the FDA and Philips — with Canadian relevance — so CPAP users know where things stand and what actions may still be required.
In 2024 and reaffirmed in 2025, the FDA has maintained the recall’s Class I status, its most serious designation.
This level applies when there’s a reasonable chance that use of the device could cause:
The FDA has reiterated its concerns about the PE-PUR sound abatement foam used in many Philips machines.
Testing showed that this foam could break down and release:
In a 2023 FDA report, testing confirmed that foam degradation could occur in a variety of environmental conditions — including normal household humidity — making previous assumptions about limited risk outdated.
Philips has continued its remediation efforts through 2025, with updates posted on its global and Canadian recall portals:
Users can still register their devices or check replacement status at: https://www.philipssrcupdate.expertinquiry.com/
Philips also released updated FAQs and user instructions in late 2024 regarding:
Although the FDA drives global device regulation, Health Canada has supported and echoed many of the FDA’s conclusions, including:
Both agencies stress that patients should not stop CPAP therapy without consulting a healthcare provider, even if the device is under recall.
As of 2025, the FDA is still:
There have been multiple legal actions in the U.S., and Canadians affected by the recall may be eligible for class-action participation, depending on provincial rulings.
If you’re still using a recalled Philips CPAP machine, it’s critical to check your registration status and speak with your provider about alternatives.
For many Canadians tired of waiting, BeC CPAP Machines provide a recall-free, fully equipped alternative:
Next: We’ll break down what actions CPAP users should take if they own a recalled device.
For Canadians using CPAP therapy, discovering that your device is under recall — especially one involving health risks — can be unsettling. But acting quickly and methodically is key to maintaining your safety without interrupting your sleep apnea treatment. Whether you use a Philips Respironics machine or are monitoring advisories from ResMed, here’s what to do next.
Start by checking whether your device is part of the official recall.
You’ll need your device’s model number and serial number, usually located on a sticker on the bottom or back of the unit.
If your device is not listed, monitor for updates — some newer recalls, such as those for certain DreamStation 2 units, are still being assessed.
If your machine is affected:
Do not stop using your CPAP machine without first consulting your sleep physician. Sleep apnea poses real health risks, and discontinuing treatment can lead to:
Your doctor can advise on whether it’s safer to continue using the device while awaiting a replacement or to seek an immediate alternative.
If your doctor recommends switching devices, you don’t have to wait months for Philips.
BeC CPAP Machines offer a proven alternative in Canada:
You can order directly with the BeC CPAP shop online or ask your sleep clinic if they partner with BeC.
“Switching to BeC CPAP meant I could sleep peacefully without worrying about foam degradation or delivery delays. I received my unit in under a week.” — Linda G., Toronto
If you’ve experienced any symptoms potentially linked to your recalled CPAP device — such as:
— it’s important to file a report with Health Canada’s MedEffect Program.
These reports help Health Canada evaluate the real-world risks associated with recalled devices.
Some local CPAP providers offer:
If you’re based in Ontario, BeC CPAP clinics can assist with same-day device assessments and transition plans.
Next: We’ll examine how the Philips DreamStation 2 is being affected by the recall process and what Canadian users are reporting so far.
As the Philips CPAP recall continues to evolve, so too do the legal consequences — particularly in North America. While much of the early litigation activity originated in the United States, Canadian legal responses have begun to gain traction, offering possible avenues for financial and health-related compensation for affected users.
This section explores the legal actions related to the Philips recall, both in Canada and internationally, with a focus on what Canadian CPAP users need to know in 2025.
The core issue stems from Philips’ use of PE-PUR (polyester-based polyurethane) foam in several of its CPAP, BiPAP, and ventilator devices.
The foam was found to degrade over time, exposing users to potentially toxic particles and gases, including compounds linked to:
Users across North America allege that Philips was aware of these risks before issuing the recall in 2021 and failed to act swiftly, leaving patients vulnerable.
In the United States, Philips has faced multiple class action lawsuits since 2021. Key legal developments include:
These U.S. cases are significant because they:
In Canada, several class action lawsuits have been filed provincially, including in:
As of 2025:
“This is about more than defective hardware. It’s about trust — and the health risks Canadian patients unknowingly faced.” — Legal counsel, Ontario Superior Court filing
Yes, but it depends on the province.
To join or stay informed:
Note: You do not have to take legal action to get your device replaced, but doing so may offer compensation for related damages.
While Health Canada is not directly involved in lawsuits, it has been:
There is growing pressure from provincial health bodies and patient advocacy groups for stronger regulation of imported medical equipment, especially in light of the Philips situation.
As of now, no legal action has been filed against ResMed in Canada. While a 2023 safety notice raised concerns about some AirSense 10 units, no lawsuits or recalls have followed.
For Canadians still using recalled or questionable devices, litigation can be a slow path to justice. If you’re looking for a practical solution today, consider switching to BeC CPAP Machines, which have:
Legal action offers one route to accountability, but it doesn’t help with sleep tonight. Stay informed, document everything, and if you’re ready for a safer option now, you don’t have to wait for the courts.
Next, we’ll look at what Canadian health agencies are saying about the risks associated with recalled CPAP machines.
Since the Philips CPAP recall first erupted in 2021, national and international health agencies have played a central role in evaluating, regulating, and communicating the risks tied to the affected devices. From Health Canada to the U.S. FDA, and extending to agencies in Europe and Asia, multiple authorities have investigated the safety of foam-degrading CPAP units — particularly those from Philips Respironics.
This section summarizes the key positions, warnings, and actions issued by major health agencies that are relevant to Canadian patients, and how their findings continue to shape public health guidance.
Health Canada is the primary agency responsible for monitoring medical device safety in Canada. Its response to the Philips recall includes:
Health Canada continues to collect and analyze reports through its MedEffect program, encouraging patients to report symptoms possibly linked to degraded foam exposure.
The U.S. FDA was the first agency to classify the Philips recall as a Class I recall, and has maintained that designation through 2025. Its findings include:
The FDA also released a timeline of Philips’ internal knowledge of the risks, raising questions about manufacturer transparency.
While the FDA and Health Canada have led most investigations, other global agencies have weighed in:
These international responses further underscore the global scale and gravity of the Philips recall.
Canadian professional bodies have also issued guidance:
Several provincial health departments have responded directly:
While major agencies work to resolve the Philips recall aftermath, Canadian patients don’t have to wait.
BeC CPAP Machines are:
Visit https://beccpap.ca to order your recall-free CPAP solution or connect with a clinic near you.
Next: We’ll explore what patients are saying in forums and support groups — and how that feedback reflects broader sentiment about the recall.
Since the Philips CPAP recall was announced in 2021, online forums and support groups — especially those catering to Canadian users — have become vital spaces for sharing firsthand experiences, concerns, frustrations, and solutions. While official reports from Health Canada and the FDA offer structured recall data, these patient-driven communities reveal the human side of the crisis.
Here’s what Canadian CPAP users are saying online, and how their stories reflect broader recall-related trends.
One of the most commonly voiced issues in forums like Reddit (r/SleepApnea), Apnea Board, and Facebook support groups is the months-long wait for replacement machines.
“Registered for a replacement DreamStation in August 2021. It’s now 2024, and I still haven’t received a new unit. I had to buy one out-of-pocket.”
Many Canadian users feel overshadowed by U.S.- based recall responses, noting that Canadian supply chains appear slower or deprioritized. Some report calling Philips or suppliers multiple times with little clarity on shipping timelines.
Numerous forum posts and threads document users experiencing new or worsening symptoms, including:
Some users only discovered their symptoms were likely linked to foam degradation after reading recall information online. Others shared that their physicians weren’t initially aware of the recall, underscoring a gap in public health communication.
“For months, I blamed my allergies. Turns out my recalled DreamStation was emitting VOCs. I wish I knew sooner.”
CPAP forums show that beyond physical symptoms, many users are experiencing high levels of stress and anxiety.
Concerns include:
This is especially true among older adults and those on fixed incomes, who rely on provincial funding or insurance to access sleep therapy.
“I’m a pensioner and can’t sleep without CPAP. But mine’s recalled, and I can’t afford to buy another. I feel stuck.”
As frustration with Philips has grown, many users have shared positive experiences switching to alternative brands, including BeC CPAP Machines in Canada.
Reported benefits include:
“Ordered a BeC CPAP machine after waiting over a year. Came fully set up and working great. No weird smells. Breathing clean again.”
Some groups have even created “safe CPAP lists” that highlight devices without a history of recalls or foam issues — BeC CPAP is often mentioned as a top choice.
Across almost every support platform, Canadian users have called for more transparent communication from Philips.
Complaints include:
Many patients have turned to forums for peer-led advice because official channels have proven slow or confusing.
“We shouldn’t have to piece together medical advice in Facebook groups. Philips and Health Canada owe us clear info.”
If you’re looking to connect with other Canadian CPAP users navigating the recall, here are some active communities:
Patient feedback from online groups highlights how the recall has affected more than just equipment — it’s affected lives.
Canadian users are demanding:
And many are choosing to take control by switching to recall-free options like BeC CPAP, proving that community knowledge can be a powerful form of advocacy.
Next: We’ll examine how the Philips recall is impacting the continuity of sleep apnea treatment in Canada — and what doctors are doing to help patients stay safe.
The Philips CPAP recall has not only disrupted equipment availability — it has directly impacted how Canadians manage their sleep apnea treatment. CPAP therapy is essential for individuals with moderate to severe obstructive sleep apnea (OSA), and any interruption, even short-term, can pose serious health risks. The recall has introduced a host of continuity challenges, from device shortages and treatment delays to patient anxiety and poor compliance.
Here’s how the recall is affecting treatment plans, what physicians are seeing, and how patients in Canada are adapting.
Continuous Positive Airway Pressure (CPAP) therapy works by keeping the airway open throughout the night.
For patients with diagnosed sleep apnea, missing even a few nights of treatment can lead to:
For this reason, any disruption in device access — as caused by the Philips recall — poses real health consequences.
“I skipped two weeks while waiting for a new unit. By the second night, I was back to waking up gasping. It set my treatment back months.” — Jordan R., Victoria, BC
Canadian patients who registered their recalled Philips units in 2021–2023 have reported wait times stretching into 12–24 months, with no definitive delivery date.
The impact includes:
Sleep specialists across Canada have voiced concern about this prolonged interruption.
Many clinics and CPAP suppliers in Ontario, Alberta, and Quebec have run out of loaner units due to the sheer volume of affected users.
Sleep clinics are also reporting:
Doctors note that recall-related stress has led to lower adherence.
Patients who once followed nightly therapy routines now:
This can cause a domino effect of deteriorating health that goes beyond sleep apnea.
The recall has also slowed down diagnosis-to-treatment timelines for new patients. Clinics are:
This leaves newly diagnosed individuals in limbo, worsening symptoms while they wait for an initial machine.
“I finally got diagnosed but couldn’t start therapy — there was no CPAP left to loan. I waited three months to get started.”
As Philips recall delays continue, many clinics and patients in Canada are turning to BeC CPAP Machines to maintain treatment continuity.
Key advantages include:
Some sleep clinics now recommend BeC as a first-line therapy option, particularly when reliability and delivery speed are essential.
“BeC let me start therapy the same week I got diagnosed. That never would’ve happened with Philips or ResMed.” — Claire M., Ottawa
The Philips recall has had a disproportionate effect on sleep apnea treatment continuity across Canada. From missed nights of therapy to postponed diagnoses, the healthcare system — and patients — are still feeling the impact.
But help is available. With Canadian-made, recall-free options like BeC CPAP Machines, treatment doesn’t have to stop. It just needs to pivot.
Next: We’ll discuss whether it’s possible — or legal — to sell or donate a recalled CPAP machine in Canada.
The CPAP landscape in Canada has shifted dramatically since the Philips recall in 2021, with consequences that are still rippling into 2025. Between ongoing legal actions, shifting medical guidelines, and rising patient frustration, it’s clear that Canadian CPAP users need reliable information and safer alternatives.
This conclusion summarizes what every user should now consider — based on Health Canada’s advisories, international health agency reports, legal trends, and real patient experiences.
If you’re using a Philips Respironics device, verify whether it’s part of the recall by:
If you own a ResMed device, especially an AirSense 10, check for performance issues but note: no Canadian recall has been issued as of late 2025.
Health Canada and the Canadian Thoracic Society both recommend:
Untreated sleep apnea can lead to serious complications. Even if your machine is recalled, stopping therapy altogether can be more dangerous.
If you’re part of the Philips recall:
Your documentation could be key in any future settlement.
If you’ve been waiting months (or years) for a Philips replacement or feel uncertain about using older devices, consider alternatives that offer:
This is where many patients are turning to BeC CPAP Machines:
“I waited two years for a replacement. Switching to BeC was the best decision for my health and peace of mind.” — Terry L., Calgary
This recall crisis has shown gaps in:
Patients and clinics alike can support:
The CPAP recall has affected hundreds of thousands of users — not just in terms of equipment, but trust, health, and peace of mind. As we move forward into 2025, Canadian CPAP users have a choice:
BeC CPAP Machines offer that stability — with no recall history and a fully compliant setup ready to go.You don’t have to wait to breathe safely again.
If you’ve been diagnosed with sleep apnea in Ontario, one of your first questions might be: “Who pays for the machine that helps me breathe at night?” The answer involves two important programs: OHIP and the ADP program (Assistive Devices Program). But they serve different roles, and it’s crucial to understand what each covers.
In Canada, the topic of CPAP machine recalls has remained at the forefront of sleep health conversations since the original Philips recall shook the market
The first two weeks set the tone. Wear your sleep apnea machine (CPAP) every time you sleep (even naps), start with short, consistent sessions, prioritise
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