An increasing number of Americans rely on sophisticated medical devices that do everything from regulating their heart rate to helping them walk. As medical devices have become more complicated, defects in manufacturing and design processes have crept in, making these devices injurious to many patients rather than beneficial.
No one implanted with a medical device expects to be injured from using this device. Unfortunately, that is exactly what happened in thousands of cases reported across the country, resulting in medical device litigation. From defective hip implant devices to malfunctioning defibrillators, there have been far too many cases of medical devices malfunctioning due to shoddy manufacturing and poor design, leaving patients with severe and long-term injuries.
Defective Medical Devices
There are many ways that a device can be defective. For instance, a medical device may be poorly designed, and due to a lack of testing, this poor design may not become obvious to the manufacturer until it is too late. A device may also be tainted with defects during the manufacturing process.
Additionally, many devices are meant only for patients with certain conditions and may have possible side effects and complications that must be made clear not just to the patient, but also to doctors. Failure to do so may cause doctors to prescribe a medical device to a patient that is not appropriate, leading to serious complications. If the manufacturer is aware of possible adverse effects, it has a duty to warn doctors and patients about the side effects.
Medical devices are expensive. They can cost thousands of dollars, and when consumers pay for a device that promises to keep them safe and healthy, they don’t expect to be injured from its use.
The danger to consumers from defective medical devices also increases because the Food and Drug Administration, the main federal body responsible for approving new medical devices, is understaffed. The agency does not have the resources to stringently review each and every medical device approval application that comes before it. As a result, the FDA often approves devices without adequate reviews, or merely because a device is similar to one already in the market.
Our Chicago Defective Medical Device Lawyers Can Help
If you’ve been harmed or injured due to a faulty medical device, don’t let the manufacturer get away with it. Let us help you file an insurance claim and get your deserved compensation. The use of insurance to cover litigation claims can be complicated and contentious, with insurers often seeking to limit their liability and healthcare providers facing potential financial strain. Further research and collaboration among stakeholders are needed to address these challenges and promote better outcomes for patients and healthcare providers.
If you or a loved one has been injured or passed away due to a medical device malfunction or medical negligence, contact the Chicago medical negligence lawyers at the Blumenshine Law Group for a free consultation or call or text us at (312) 766-1000.


