Remstar Pro M Series Recall | Is Remstar Pro Cpap Recalled?

Let’s talk about the ResMed Star Pro M-Series CPAP and Heated Humidifier System recall. It’s true that this particular system was recalled in 2009 (Recall # Z-1260-2009). This recall specifically affected the models with catalog numbers 1049109, 1049110, 1049111, and AC1049109.

It’s important to understand why this recall happened. The ResMed Star Pro M-Series CPAP was recalled because the humidifier chamber had a potential for a mold buildup which could affect the overall health and well-being of the user. Mold growth can cause respiratory issues and other health problems, especially for those with compromised immune systems. ResMed took this potential health hazard very seriously and decided to initiate a recall to ensure the safety of their users.

So, if you have an older ResMed Star Pro M-Series CPAP system, you might want to check the catalog number to see if your model was part of the recall. If it was, it’s important to contact ResMed or your medical provider to learn more about the recall and the available options.

It’s always important to prioritize your health and well-being. If you have any concerns about your CPAP system or its potential impact on your health, don’t hesitate to reach out to your medical professional.

You can find your CPAP’s serial number on the bottom label. Serial numbers are unique identifiers that are used to track specific devices. If you’re concerned about a recall, you can use your serial number to check if your CPAP machine is included in the recall list.

You can find a list of recalled CPAP machines on the Philips website. This list will provide you with the specific model numbers and serial numbers of the devices that have been recalled. You can also contact Philips directly to verify if your specific CPAP machine is part of the recall.

It’s important to note that not all CPAP machines have been recalled. You can use the serial number on your machine to determine if it’s part of the recall. You can also check with your doctor or sleep clinic to see if they have any information about the recall.

CPAP machine recalls are a serious matter, and it’s important to take them seriously. If your CPAP machine has been recalled, you should stop using it immediately and contact Philips to get more information about the recall. You may also need to contact your doctor to discuss your treatment options.

The REMstar Pro M Series with C-Flex is a great option for those seeking a comfortable and effective treatment for sleep apnea. It combines the C-Flex technology with optional integrated humidification and the Encore Pro SmartCard, providing you with powerful insights into your sleep health. This includes detailed reports on your apnea/hypopnea index, elevated leak levels, and snoring, empowering you to better manage your condition.

The C-Flex technology in the REMstar Pro M Series is designed to provide you with personalized pressure adjustments throughout the night. It automatically senses your breathing patterns and adjusts the pressure accordingly, ensuring a comfortable and effective treatment. This technology makes it easier to fall asleep and stay asleep throughout the night.

Integrated humidification is available as an optional feature for those who experience dryness in their nose and throat. This feature adds moisture to the air delivered through the mask, promoting a more comfortable sleep experience. It helps reduce the discomfort often associated with dry air during treatment.

The Encore Pro SmartCard is a powerful tool for managing your sleep apnea treatment. It allows you to monitor your progress, providing detailed reports on your sleep quality and treatment effectiveness. You can track your apnea/hypopnea index, elevated leak levels, and snoring over time, allowing you to see how your treatment is working and make any necessary adjustments with your doctor.

The apnea/hypopnea index measures the number of times you stop breathing or have shallow breaths per hour of sleep. Elevated leak levels indicate that there is a gap between your mask and your face, which can affect the effectiveness of your treatment. Snoring is another important indicator of sleep apnea, and the Encore Pro SmartCard can help you monitor your snoring patterns.

By providing this comprehensive data, the Encore Pro SmartCard helps empower you to take control of your sleep apnea and optimize your treatment. You can work with your doctor to make informed decisions about your therapy, ensuring you are getting the most effective treatment possible.

Philips Respironics makes the REMstar Pro 2 C-Flex CPAP machine.

Philips Respironics is a well-known and trusted brand in the medical device industry. They have a long history of developing innovative and effective solutions for sleep apnea and other respiratory conditions. The REMstar Pro 2 C-Flex is just one of their many popular CPAP machines, and it’s known for its advanced features and comfortable design.

When you’re looking for a CPAP machine, it’s important to choose one that’s made by a reputable company. Philips Respironics has earned a strong reputation for quality and reliability, so you can be confident that their products will meet your needs.

Philips, a leading manufacturer of CPAP devices, issued a recall in June 2021 for several products that contained a specific type of foam called PE-PUR. This foam was later linked to potential health risks, including cancer. The affected CPAP machines included the DreamStation CPAP, Auto CPAP, and BiPAP.

The specific CPAP machines that have been linked to potential health risks are the DreamStation series, including the DreamStation CPAP, Auto CPAP, and BiPAP. These models, manufactured by Philips, utilized a foam called PE-PUR which has been identified as potentially emitting harmful chemicals. This foam was designed to improve the comfort and quietness of the machines, but it was later found to degrade over time and release harmful chemicals. These chemicals have been linked to potential health risks, including cancer.

It is important to note that not all CPAP machines are affected by this issue. The recall primarily applies to Philips-branded CPAP machines produced between 2009 and 2021, specifically those containing the PE-PUR foam. If you have a Philips CPAP machine, it’s essential to check if your model is included in the recall and contact Philips for guidance. They will provide you with information on how to safely dispose of your device and receive a replacement.

It’s important to contact your doctor right away if you’re using a recalled CPAP or BiPAP machine. They’ll be able to guide you on what to do next based on your individual needs and circumstances. They may suggest you stop using your device immediately or continue using it until you get a safe replacement.

Here’s why it’s crucial to talk to your doctor about a recalled CPAP machine:

Safety First: Recalled machines may pose health risks due to issues like faulty parts or potential contamination. Your doctor can assess the specific risks associated with your machine and advise you on the best course of action.
Alternative Options: Your doctor can discuss alternative CPAP or BiPAP machines that are safe to use while you wait for a replacement for your recalled device. They may even recommend other sleep apnea treatment options if necessary.
Peace of Mind: Talking to your doctor will provide you with the information you need to make informed decisions about your treatment and ensure your safety. It can also ease any worries you might have about continuing to use your current machine.

Remember, your health is paramount. Don’t hesitate to reach out to your doctor for guidance if you are using a recalled CPAP or BiPAP machine. They are there to help you make the safest and most effective choices for your sleep apnea treatment.

ResMed recently announced a recall of some of their AirFit and AirTouch CPAP masks. The Food and Drug Administration (FDA) classified this recall as Class I, meaning the situation is considered to be life-threatening. This recall affects 20.4 million masks that were distributed in the US between January 2020 and November 20, 2023. You can find the specific product codes and model numbers listed on the FDA’s website.

It’s important to understand why this recall was issued. The FDA determined that some of these masks could potentially pose a health risk to users. The foam used in the masks could break down and be inhaled by the user. This could lead to serious problems, including lung irritation and inflammation. If you’re using one of the recalled masks, it’s crucial to stop using it immediately and contact your doctor. You can also visit the FDA website for more information on the recall and how to get a replacement mask. Remember, your health and safety are a top priority.

What to do if your mask is recalled:

Stop using the mask immediately.
Contact your doctor or healthcare provider. They can provide guidance on alternative treatment options and how to get a replacement mask.
Visit the FDA website for a comprehensive list of recalled masks and model numbers.
Contact ResMed for more information about the recall and replacement options. They have a dedicated customer service line for this specific recall.

This recall highlights the importance of staying informed about product safety information. By taking these steps, you can ensure you’re using a safe and effective CPAP therapy that meets your needs.

You might be wondering if your CPAP is safe, especially after the FDA recall of some Philips CPAP machines. Don’t worry, you don’t need to stop using your CPAP immediately.

The best course of action is to talk to your doctor. They can give you the most accurate information about whether or not it’s safe for you to continue using your specific CPAP machine.

Here’s why talking to your doctor is crucial:

They understand your individual needs: Your doctor is aware of your health history, the severity of your sleep apnea, and any other medical conditions you have. This allows them to assess the risks and benefits of continuing CPAP therapy for you.
They can access the latest information: The FDA is constantly updating its information and recommendations regarding recalled CPAP machines. Your doctor will have access to this information and can provide you with the most current guidance.
They can help you find alternatives: If your doctor determines that your CPAP is unsafe, they can help you explore other treatment options, such as different CPAP models, alternative therapies like oral appliances, or even surgery.

It’s important to remember that not all CPAP machines were recalled, and even within the recalled models, the level of risk can vary depending on the specific machine and the individual patient. Your doctor will be able to help you navigate this complex situation and make the best decision for your health.

Philips is committed to resolving this issue and ensuring the safety of all patients. They are repairing or replacing all devices affected by the recall, no matter how old the device is. If a replacement is necessary, it may be the same model or a different Philips device that meets the patient’s needs.

This commitment to remediation shows Philips’ dedication to patient safety. They understand that a recalled device can be a source of worry for patients. That’s why they’ve designed a comprehensive plan to ensure that every affected device is addressed in a timely manner.

Here’s what you can expect if your device has been recalled:

Contact Philips: The first step is to contact Philips directly. They have a dedicated team ready to assist you with any questions or concerns you may have.
Device Assessment: Philips will assess your device to determine if it needs repair or replacement.
Repair or Replacement: Depending on the assessment, your device will either be repaired or replaced. If it’s replaced, you’ll receive a similar device or one that meets your specific needs.
Convenient Process: Philips will work with you to make the repair or replacement process as convenient as possible.

If you have any questions or concerns about the recall or the remediation process, don’t hesitate to reach out to Philips directly. They are committed to providing you with the information and support you need.

In June 2021, Philips Respironics announced a recall of certain CPAP, BiPAP, and ventilators. The recall was due to a potential issue with the sound abatement foam used in these devices. This foam could degrade and break down into small particles, which could be inhaled by the user.

The company had initially issued a field safety notice in April 2021, alerting users to the potential issue. However, following that initial notice, Philips Respironics received a significant increase in complaints related to the foam degradation problem. This increase in complaints highlighted the seriousness of the issue and led to the full-scale recall.

Here’s why the recall was necessary:

Health Risks: The degraded foam could potentially pose health risks to users, including respiratory issues, irritation, and even long-term health problems.
Safety Concern: The presence of the foam particles in the breathing circuits could pose a safety hazard, particularly for individuals with sensitive respiratory systems.
Product Performance: The foam degradation could also affect the performance and effectiveness of the respiratory devices, potentially compromising their intended use.

The recall was a proactive measure by Philips Respironics to address these potential risks and ensure the safety and well-being of their users. It’s important to note that not all devices were affected by the foam issue, and the recall specifically targeted models using certain types of sound abatement foam.

The recall process involved informing affected users, providing replacement devices or repair options, and working with healthcare professionals to ensure patients received proper care. While the recall was a significant event, it demonstrated Philips Respironics’ commitment to user safety and their proactive approach to addressing potential product concerns.

You can register for a Philips recall in two easy ways:

1. Visit the Philips recall website.
This is the fastest and most convenient option. You’ll find all the information you need and be able to register your device quickly.

2. Call the Philips recall hotline at 1-877-907-7508.
This is a great option if you prefer to speak with someone directly. A Philips representative will be happy to answer any questions you may have and guide you through the registration process.

Philips is committed to ensuring the safety and well-being of its customers. They’re working closely with Health Canada and their Canadian network of Durable Medical Equipment Providers (DMEs) to make sure everyone gets the help they need.

Here’s what you need to know about the Philips recall process:

Philips will contact you directly. Once you register, Philips will contact you about the next steps. They may ask you to return your device for repair or replacement.
The recall process may take some time. Philips is working diligently to ensure a smooth and efficient process. Be patient and know that they’re working hard to get your device fixed or replaced as quickly as possible.
You can check the status of your recall online. Philips provides an online portal where you can check the status of your recall at any time. This will keep you updated on the progress of your repair or replacement.

The Philips recall process can seem daunting, but it’s actually quite straightforward. By following the steps above, you can easily register your device and get the help you need.

Philips has reached an agreement with private plaintiffs in the United States to settle all economic loss claims related to the Philips Respironics voluntary recall of certain sleep and respiratory care devices. This agreement is subject to final court approval.

This settlement signifies a positive step towards resolving the issues arising from the recall. It provides a path forward for individuals who experienced economic losses due to the recall. The agreement will offer compensation to those affected and aims to provide closure and peace of mind.

What does this recall agreement mean for affected individuals?

This agreement is a significant development for individuals who have been affected by the Philips Respironics recall. Here’s a breakdown of what it entails:

Resolution of Economic Loss Claims: The agreement covers economic loss claims brought by private plaintiffs in the United States. This means that individuals who suffered financial losses due to the recall, such as the cost of replacement devices, medical expenses, or lost wages, can potentially seek compensation.
Final Court Approval Pending: The agreement is still subject to final approval by the court. This process involves legal review and may take some time. Once approved, the settlement will be finalized.
Closure and Peace of Mind: This agreement offers a path towards closure for those impacted by the recall. It provides a mechanism for seeking compensation and hopefully alleviates the stress and inconvenience associated with the situation.

How Can Affected Individuals Learn More?

Individuals who have been affected by the Philips Respironics recall should keep an eye out for official communication from Philips and the court regarding the settlement. They can also consult with legal counsel to understand their specific rights and options. This agreement represents a step toward resolving the issues stemming from the recall, providing a path forward for affected individuals and Philips.

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