Philips Respironics Recall 2021 {June 2021} Read & Know!

Philips Respironics Recall 2021 {June 2021} Read & Know! >> The guide shares comprehensive details about the defective ventilators and CPAP breathing devices used to treat patients worldwide.

Has anyone in your community used Philips Ventilator? Then you must follow this article to know all the key facts about the machine.

Philips Respironics, a global healthcare firm, is known as a leader in the Sleep and Respiratory market, which believes in three healthier terms as healthier patients lead to healthier practices, and after that produces healthier businesses.

Most of the people in the United States and Canada have obstructive sleep apnea, and for these people, Philips Respironics tries to provide the best solutions, and Philips Respironics Recall 2021 is one of their approaches.

About Philips Respironics

Philips Respironics offers various innovative and unique products for treating sleep and respiratory diseases at home or in hospitals. The company also contributes to the medical education field and value-added programs to maximize business success and help you easily navigate in a fast-changing industrial field.

As we all are aware of Corona, it is a pandemic respiratory disease that hits almost every country at a fast rate. In this situation, the requirement for respiratory tools increases day by day.

Philips Respironics Recall 2021

On 14th June, Philips, a Dutch medical devices company has recalled their 3-4 million ventilators like E30 Ventilator, the Trilogy 100, and 200 ventilators and sleep apnea machines because of some problem seen in the machines. 

Like, degrading of foam particles take place which leads to the release of harmful gases. These gases can easily inhale by users, which can cause health-threatening diseases like cancer, as per reports and sources.

Beneficial Key Facts

• Company identifies sound diminishing foam element
• Inhaling of degraded foam component can cause cancer
• Advices Restricted usage of CPAP machine by sleep apnea patients
• Company will mitigate the issue by replacing the foam.
• Philips Respironics Recall 2021 is for the United States. It is simply a safety notice for other countries.

Health Risks and Repair Program

Philips Respironics provides advice to patients using CPAP machines to stop using it but for COVID-19 patients. Using a ventilator is only the option for their life-sustaining; therefore, advising them not to discontinue it is riskier than the issue found in the recall.

The potential health risks caused by this foam include headache, toxic effects, irritation, respiration choke and also can cause cancer.

In Philips Respironics Recall 2021, the company says it will replace the toxic foam with new material. The whole diagnostic and repairing will probably be ready in a year, cost going up to 500 million Euros. Therefore, Philips increase the production of the next-generation DreamStation 2 CPAP Platform free from this issue.

Update on Recall Notifications by Philips

After the recall notification, Philips issued an update against the notifications for its Bi-Level Positive Airway Pressure, Continuous Positive Airway Pressure and other Mechanical Ventilator Devices. They confirmed to address the identified health risks associated with the devices. As per sources, here are some steps that are taken against the Philips Respironics Recall 2021:  

• The company started a voluntary recall notification for ensuring the safety of the patients in coordination with respective regulatory agencies. 

• A few corrective steps include implementing updated instructions for the usages, replacement, and repair program for malfunctioning devices.

• Philips focuses on repairing the malfunctioning devices at the earliest with minimal downtime.    

Respironics Recall Notification 2021 – Advice for Customers and Patients

Based on the study on potential health risk, the Philips Respironics Recall 2021 notification advises customers and patients to take the following measures. 

• Discontinue the usages of affected CPAP and Bi-Level PAP devices with immediate effect. Patients and customers must approach the physician or the DME provider to identify the apt option for further treatment. 

• Discontinue the usages of malfunctioning life-sustaining mechanical ventilators or change the recommended therapy after discussion with your doctor. As per the sources, the alternate ventilator options for the treatment may not exist and are limited for patients who seek a ventilator for life-sustaining treatment. So, it is advised to seek suggestions from the doctor before discontinuing the treatment with life-sustaining mechanical ventilators.

Conclusion

The above research reveals that Philips Respironics is the medical company dealing in sleep and respiratory disease equipment. On 14th June, under Philips Respironics Recall 2021, they announced recalling 3-4 million ventilators and CPAP machines due to the risk of degrading a foam part that can cause cancer, as per the sources.  

However, they plan to mitigate the problem, which can take a year and cost up to 500 million Euros, the report confirms. You can check complete detail here.

Are you the victim of the faulty device? Have you reported the issue? Please share your experience in the comment section below. Moreover, this information is elaborated here as per the sources and after gathering details from the internet. We are not the authority of the subject.

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