Our Attorneys Fight for Defective Medical Devices Injuries

Firm in The Carolinas and Virginia seeks justice for victims

A defective medical device presents an additional threat to someone who is already suffering from a physical aliment. Though people frequently hear stories about recalled products, they often don’t understand that some of these devices are not thoroughly screened by the Food and Drug Administration (FDA). The review system varies based on the type of product involved and its use. When recalls occur, they fall into one of three classes set forth by the FDA.

Class I is the most serious, indicating that there is a reasonable chance that a product will cause serious health problems or death. Class II is reserved for instances in which the harm is temporary or a slight chance of serious damage exists. If the unlawful product is not likely to provoke an injury or illness, it is categorized as Class III.

Regardless of the specific device involved, if you believe that you’ve been negatively affected by a recalled item or some other faulty medical implant, Marcari, Russotto, Spencer & Balaban can advise you of your legal rights and options.

Lawyers bring actions against manufacturers of faulty healthcare products

Bringing a case against a medical device manufacturer demands a mass tort lawyer who can challenge large corporations and gather the necessary technical evidence. We deliver compelling arguments in all types of claims, such as those pertaining to:

• IVC Filter Failures – IVC (Inferior Vena Cava) filters are implanted in patients at risk of blood clots to prevent them from reaching the lungs and causing a pulmonary embolism. Unfortunately, these filters can fracture or migrate to other parts of the body, leading to serious and sometimes fatal complications, including organ damage, deep vein thrombosis, and heart or lung perforation. Studies have shown that up to 40% of IVC filters may fail, and manufacturers like C.R. Bard have faced thousands of lawsuits, with significant settlements awarded to affected patients.
• Paragard IUD Complications – The Paragard IUD, a popular non-hormonal birth control device, has been associated with dangerous complications during removal. There have been numerous reports of the device breaking upon removal, leaving fragments in the uterus that can cause severe pain, infection, and uterine perforation. These issues may necessitate further surgeries and, in some cases, lead to hysterectomy. Paragard’s manufacturer, Teva Pharmaceuticals, is currently facing a growing number of lawsuits, as women seek compensation for these life-altering injuries.
• Philips CPAP Device Recall – In 2021, Philips issued a massive recall of its CPAP, BiLevel PAP, and mechanical ventilator devices after it was discovered that the foam used in these devices could degrade and release toxic particles. These particles have been linked to a range of health issues, including respiratory problems, lung cancer, and organ damage. The recall affected millions of devices worldwide, and numerous lawsuits have been filed by users who have suffered from serious health conditions. Philips has set aside over $500 million for potential settlements as the litigation continues to grow.

Problems with medical devices and implants continue to be discovered. If you believe you have been hurt by a surgical or medical care product, you need the assistance of an experienced attorney.

Contact a lawyer for a free consultation regarding a defective medical device claim

Marcari, Russotto, Spencer & Balaban represents plaintiffs in matters relating to recalled and defective medical devices.

Please call (855) 435-7247 or contact us online to schedule a free initial consultation at one of our offices, located in North Carolina, South Carolina & Virginia.