Philips Suspends Sales of Breathing Machines in the U.S. After Major Recall

In a significant turn of events, Philips Respironics has taken a bold step by announcing the suspension of all sales of its breathing machines within the United States. This decision comes on the heels of a comprehensive settlement with the Food and Drug Administration (FDA) regarding ongoing issues with their CPAP (Continuous Positive Airway Pressure) and ventilator devices.

At the core of this tumultuous development are the unsettling reports of these devices expelling small particles of foam and potentially harmful gases into the airways of unsuspecting consumers. The repercussions of this malfunction have sent shockwaves through the medical community and raised questions about the safety of millions of Philips breathing machines in circulation.

As part of the settlement with the FDA, Philips is obligated to undergo a substantial overhaul of its operations, encompassing a multiyear plan, before it can resume its sales activities in the United States. The specifics of this agreement are yet to be fully disclosed, pending finalization in court. However, Philips has committed to maintaining its services for existing device users while making necessary repairs.

This recall saga initially unfolded in June 2021 when Philips embarked on the recall of numerous devices and suspended the sale of new sleep therapy machines in the U.S. The primary concern at that time was the potential for severe injuries and permanent impairments arising from the release of potentially carcinogenic chemicals by these devices.

Subsequently, Philips conducted additional testing, asserting that their devices were unlikely to cause significant harm to patients’ health. However, their updated claims faced skepticism from the FDA, which referred to them as “unpersuasive.” In response to this scrutiny, Philips initiated further recalls in an attempt to enhance the safety and reliability of their products.

In light of these developments, many individuals have suffered harm and injury as a result of using these faulty breathing machines. Victims of this issue may consider pursuing legal action to seek compensation for their injuries through a product liability lawsuit. Such lawsuits are designed to hold manufacturers accountable for producing and distributing defective products that cause harm to consumers.

How to Begin the Injury Lawsuit Process

The process of filing a product liability lawsuit can be complex, requiring the expertise of an experienced attorney at each step. Victims should seek legal representation to navigate the following stages:

1. Free Consultation: Victims should schedule a consultation with an attorney to discuss the specifics of their case. During this initial meeting, the attorney will assess the viability of the lawsuit and provide guidance on the best course of action.
2. Investigation: The attorney will conduct a thorough investigation to gather evidence establishing the product’s defect, its connection to the injuries sustained, and the extent of damages suffered by the victim.
3. Filing the Lawsuit: Once the attorney has gathered sufficient evidence, they will file a product liability lawsuit on behalf of the victim against the manufacturer, in this case, Philips Respironics.
4. Discovery: The discovery phase involves exchanging information between both parties. The manufacturer’s defense team will present their evidence, and the victim’s attorney will continue to build their case.
5. Negotiation or Trial: In some cases, negotiations may occur between the parties to reach a settlement. If an agreement cannot be reached, the case proceeds to trial, where a judge or jury will determine liability and potential damages.
6. Damages: In the event of a successful lawsuit, victims may be entitled to various forms of compensation, including medical expenses, lost wages, pain and suffering, and punitive damages.

It is crucial for victims of injuries caused by defective Philips breathing machines to seek legal representation, as an attorney can provide essential guidance, advocacy, and expertise throughout this complex legal process.

The suspension of Philips Respironics’ sales in the United States following a product recall underscores the gravity of the situation and the potential harm these devices have caused. Victims have legal avenues to pursue compensation for their injuries, and seeking the counsel of an experienced attorney is paramount in navigating the complexities of a product liability lawsuit. Don’t hesitate to take action and reach out to reputable law firms like Parker Waichman LLP to protect your rights and interests.

Contact Parker Waichman LLP For A Free Case Review

For those harmed by these troubling incidents, contact the national product injury law firm of Parker Waichman LLP for your free consultation. By calling 800-968-7529, you can take the first step toward seeking justice and financial compensation for the harm you or a loved one has endured.

Regardless of your location or where your injury occurred, our nationwide personal injury law firm is ready to assist you.