A: Philips recalled CPAP machines because of the materials used to make some of the foam in these devices. This foam was found to degrade over time, which can make it detach from the device and be inhaled by users of the machine. Additionally, other unsafe chemicals could be created through the maintenance of the machine, especially if the individuals using it cleaned it with ozone cleaners. Issues include breathing problems, headaches, and organ issues.
Baton Rouge Philips CPAP & Bi-PAP Recall Lawyer
The recent recall from Philips shows how important product safety is and how many consequences can occur due to manufacturing defects. Users of certain Philips CPAP devices, who rely on them for respiratory support, now face the overwhelming task of replacing their units and obtaining medical treatment for their injuries. Given the gravity of the situation, affected individuals should contact a skilled Baton Rouge Philips CPAP & Bi-PAP recall lawyer at Murphy Law Firm.
Philips Medical Product Issues
On June 15, 2021, Philips recalled over 3 million CPAP, Bi-Level PAP and mechanical ventilator devices for potential health risks related to the sound abatement foam. Most of the defective devices are in the first-generation Dream Station product family.
Here’s a list of all the recalled Philips devices.
The reason for the recall is due to the degradation of the polyester-based polyurethane (PE-PUR) sound abatement foam in the devices may result in increased health risks. The foam may degrade into particles that are then ingested or inhaled by the user. The foam may also off-gas certain chemicals that are hazardous to the user.
Philips’ Recalled Devices
CPAP & BiPAP Devices
Continuous Ventilator, Minimum Ventilatory Support (Facility Use):
- E30 (Emergency Use Authorization)
Continuous Ventilator, Non-life supporting:
- DreamStation ASV
- DreamStation ST, AVAPS
- SystemOne ASV4
- C-Series ASV
- C-Series S/T and AVAPS
- OmniLab Advanced+
Noncontinuous Ventilator:
- SystemOne (Q-Series)
- DreamStation
- DreamStation Go
- Dorma 400
- Dorma 500
- REMstar SE Auto
Mechanical Ventilators
Continuous Ventilator:
- Trilogy 100
- Trilogy 200
- Garbin Plus, Aeris, LifeVent
Continuous Ventilator, Minimum Ventilatory Support (Facility Use):
- A-Series Bi-PAP V30 Auto
Continuous Ventilator, Non-life Supporting:
- A-Series BiPAP A40
- A-Series BiPAP A30
Types of Injuries Potentially Related to Philips Product Recall
According to Philips, these are the potential health risks related to this recall:
- Degraded foam exposure may cause: Irritation (skin, eye and respiratory tract), inflammatory response, headache, asthma, adverse effects to other organs (e.g. kidneys and liver) and toxic or carcinogenic affects.
- Chemical emission exposure may cause: headache/dizziness, irritation (eyes, nose, respiratory tract, skin), hypersensitivity, nausea/vomiting, toxic and carcinogenic effects.
What Do I Do If I Have an Affected Device?
If you have a dangerous medical product, it’s important to deal with it accordingly. Philips has a program in place where individuals with an affected device can return it to the company so that they can repair the defect and send it back out. Many individuals have probably already been contacted by their Durable Medical Equipment providers (DMEs) to replace their devices. If you have not, visit the Philips recall website for more information.
Hire Baton Rouge Personal Injury Attorney
If you’ve been in contact with any of the recalled defective devices and experienced any of the types of injuries listed above, you should contact a local personal injury attorney in Baton Rouge today. At Murphy Law Firm, we fight for you! If you don’t win, we don’t get paid. It’s that simple. So, contact our experienced Baton Rouge personal injury lawyers today and get a free consultation.
FAQs
Q: What Should I Do If I Have a Recalled Philips CPAP Device?
A: If you have a recalled Philips CPAP device, you should stop using it immediately. Contact your doctor or healthcare provider to develop alternative treatment options for your health conditions, like using another device. If you have encountered any problems with your device, you can report them via the FDAs MedWatch. Finally, register your device on the recall website to receive updates on the recall product..
Q: What Legal Options Do I Have If I Have Been Affected by a Recalled Philips CPAP Machine?
A: If you have been affected by a recalled Philips CPAP machine, you might be eligible for financial compensation by filing a claim against Philips. To start this process, contact a personal injury attorney. They can review your case and inform you of the evidence you might need to file a claim for damages related to the recalled device, including medical care to recover from any injuries caused by the recalled device.
Q: What Happens If I Don’t Return My Philips CPAP?
A: If you do not return your Philips CPAP, then you might be billed for the cost of a replacement device if you are given one. If you choose to preserve your own unit, then you must register it in Philips’ Preservation Registry. The company asks that patients return their defective CPAP devices so that they can repair and replace them. For more information on the CPAP recall, contact a product liability attorney.
Protect Your Health After the Philips CPAP Recall
If you’ve been affected by the recent Philips recall, take action now. The potential health risks associated with the degraded foam in the machines are serious and can greatly impact your well-being. Schedule a consultation with Murphy Law Firm today for an effective evaluation of your case. We are dedicated to fighting for your rights and securing your deserved compensation.
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