Philips MRI Scanner
Philips, a prominent medical device maker, is facing a critical situation with the recall of 150 of its magnetic resonance imaging (MRI) scanners, specifically the Panorama 1.0T open MRI systems. This recall has been triggered by a potentially hazardous issue: the risk of an explosion due to the build-up of excessive pressure from helium gas within the machines. This situation is distinct from Philips’ previous recalls, which primarily focused on their respiratory device product line. The company has issued an urgent medical device correction notice to users of the affected MRI systems, highlighting the seriousness of the issue.
The United States Food and Drug Administration (FDA) has classified this recall as a Class I recall, the most severe category, indicating that continued usage of these devices could result in serious injuries or even fatalities. The FDA, in an alert issued on December 20, explained that the explosion risk is particularly high during a process known as a quench. This procedure involves the rapid expulsion of liquid cryogen to maintain the superconductivity of the MRI magnet. Additionally, unintended quenches can also lead to dangerous scenarios. In either case, the pressure build-up could compromise the structural integrity of the device, posing significant risks.
The potential dangers in the event of an explosion are substantial. Patients could be exposed to harmful chemicals and suffer from a lack of oxygen, not to mention the traumatic injuries caused by the explosion itself. The FDA emphasized the risk of tissue damage and mechanical trauma from debris, which could lead to severe brain injury or even death. Despite the severity of these risks, there has only been one reported explosion in the 22 years these systems have been in use, with no injuries or deaths reported to date.
In response to this issue, Philips has advised customers to stop using the affected scanners and has specifically cautioned against performing a manual quench of the magnet, except in emergencies. The FDA has clarified that this action is a correction rather than a complete withdrawal of the product from the market. According to a GlobalData report, Philips holds approximately 13% of the global MRI device market, which is valued at an estimated $5.2 billion in 2023.
Victims affected by this issue might consider the possibility of filing a product liability lawsuit to seek damages. Such lawsuits are typically filed against manufacturers for producing or selling a defective product that causes harm. In this case, the lawsuit would argue that Philips’ MRI scanners were inherently dangerous due to the risk of explosion. The legal process for filing a product liability lawsuit involves gathering evidence, filing a complaint, and possibly going to trial. Each step requires the expertise of a specialized attorney who can navigate the complexities of the legal system, advocate for the victim’s rights, and negotiate settlements.
In a product liability lawsuit, victims can seek compensation for various types of damages, including medical expenses, lost wages, pain and suffering, and in some cases, punitive damages. The role of an attorney is crucial in accurately assessing and claiming these damages to ensure a fair resolution for the victim.
CONTACT PARKER WAICHMAN LLP FOR A FREE CASE REVIEW
For those harmed by this Philips MRI scanner, the national product injury law firm Parker Waichman LLP is offering legal assistance. The firm provides a free consultation service, which can be accessed by calling 1-800-YOUR-LAWYER (1-800-968-7529). Parker Waichman LLP’s commitment to representing victims of product-related injuries highlights the importance of addressing safety concerns and ensuring justice for those adversely affected.
No matter your location or where your injury happened, our nationwide personal injury law firm stands ready to help you.
