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The U.S. Food and Drug Administration (FDA) has recently highlighted concerns regarding certain Resmed masks, which have been linked to six patient injuries due to their magnetic components. This development follows a product correction initiative by Resmed and the FDA’s classification of this action as a Class I recall, indicating a high risk of […]
Resmed Mask Lawsuits
The U.S. Food and Drug Administration (FDA) has recently highlighted concerns regarding certain Resmed masks, which have been linked to six patient injuries due to their magnetic components. This development follows a product correction initiative by Resmed and the FDA’s classification of this action as a Class I recall, indicating a high risk of serious injury or death.
Resmed first initiated customer contact in November, acknowledging that the magnets embedded in their positive airway pressure therapy masks could potentially interfere with active implants and metallic medical devices. This interference poses a significant health risk to users with such medical devices. At the time of their initial notice, Resmed reported no permanent injuries or fatalities related to this issue. However, the possibility of serious injury or death due to magnetic interference led the FDA to categorize the correction as Class I.
In December, the FDA added the product correction to its recall database, underscoring the severity of the situation. The latest FDA statement, released on Thursday, discusses the correction of over 20 million Resmed masks sold in the U.S. between January 2020 and November 2023. This statement reemphasizes the guidance from Resmed’s urgent field safety notice, particularly the recommendation to keep the masks’ magnets at least six inches away from susceptible medical devices.
The FDA’s notice, while confirming six reported injuries, does not provide detailed information about the nature of these injuries. This situation is reminiscent of a previous incident involving 17 million magnetized masks from Philips, Resmed’s competitor, which were linked to 14 serious injuries, including complications like pacemaker failure, arrhythmia, seizures, and irregular blood pressure.
For individuals who have suffered injuries due to the magnetic interference of Resmed masks, legal recourse is available. Victims may consider filing a product liability lawsuit to seek compensation for their injuries. Such a lawsuit typically involves proving that the product was defective and that this defect directly led to injury or harm. The lawsuit process can be intricate, involving evidence collection, establishing the link between the product and the injury, and demonstrating the impact of the injury on the victim’s life.
Navigating a product liability lawsuit requires the expertise of a skilled attorney, who can guide victims through each stage of the process, from filing the lawsuit to potentially reaching a settlement or court verdict. An attorney is instrumental in ensuring that all legal requirements are met and that the victim’s case is presented effectively. Compensation in product liability cases can cover medical expenses, lost income, pain and suffering, and in cases of severe negligence, punitive damages.
For those affected by the issues with Resmed’s magnetized masks and considering legal action, Parker Waichman LLP, a national product injury law firm, offers expert legal advice and representation. They provide a free consultation to discuss the specifics of your case. To explore your legal options and understand the steps involved in pursuing a product liability lawsuit, contact Parker Waichman LLP at 1-800-YOUR-LAWYER (1-800-968-7529). Their experienced team is committed to helping you seek justice and fair compensation for the harm you have endured. Don’t hesitate to reach out for the guidance and support you need during this challenging time.
Regardless of your location or where your injury occurred, our nationwide personal injury law firm is ready to assist you.