What is the role of the manufacturers and distributors of medical devices in medical device injury cases?

Manufacturers and distributors of medical devices play an important role in medical device injury cases in Illinois. Medical device manufacturers are responsible for designing, testing, and producing medical devices. These manufacturers must comply with regulations established by the United States Food and Drug Administration (FDA) in order to ensure safety and effectiveness. Distributors are then responsible for selling the medical devices, ensuring proper installation and usage instructions, and providing maintenance and other support services. When a patient is injured due to a medical device, manufacturers and distributors may be liable if it can be proven that the device was either defectively designed or manufactured in some way, or that there were inadequate instructions or warnings that contributed to the injury. A patient or their family may sue the manufacturer or distributor of a faulty medical device, seeking compensation for the cost of medical treatment, lost wages due to inability to work, and other damages. In order to prove the manufacturer or distributor liable for their product’s malfunction or injury, the plaintiff must demonstrate that the device’s design or manufacture was negligent or unreasonably dangerous, or that the manufacturer or distributor provided inadequate instructions or warnings about the device’s use. If it is determined that the manufacturer or distributor is liable, the plaintiff may receive both economic and non-economic damages.

What is the role of the manufacturers and distributors of medical devices in medical device injury cases?

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