Every February, American Heart Month serves as a crucial reminder of the importance of heart health. For many individuals, life-saving heart surgeries involve the use of medical devices such as pacemakers, stents, and artificial valves. While these devices are designed to improve and extend lives, some may unfortunately be defective, leading to severe health complications or even loss of life. Victims of defective heart-related medical devices have legal rights, and it is essential to understand the options available for seeking justice.
The Impact of Defective Medical Devices on Heart Surgeries
Defective medical devices can cause serious complications, including heart failure, infections, blood clots, or device malfunction. In some cases, a recall may be issued, but often, patients suffer harm before a defect is identified. Common defects include:
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Faulty pacemakers that stop functioning correctly
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Stents that collapse or cause clotting
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Artificial valves that degrade prematurely
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Implantable defibrillators that fail to deliver life-saving shocks
These defects can result in repeated surgeries, additional medical expenses, emotional distress, and long-term health issues.
Legal Rights of Victims
Patients who experience harm due to a defective medical device have legal recourse under product liability laws. There are three primary types of claims:
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Design Defect: The device was inherently flawed in its design, making it unsafe for patients.
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Manufacturing Defect: Errors in the manufacturing process resulted in a faulty product.
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Failure to Warn: The manufacturer failed to properly warn doctors and patients about known risks or defects.
Additionally, medical professionals who use these devices may bear some responsibility if they fail to adhere to standard procedures. Healthcare providers, including surgeons and cardiologists, must exercise due diligence when selecting and implanting medical devices. They are expected to:
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Properly evaluate the risks associated with a specific device before use.
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Stay informed about product recalls and FDA safety alerts.
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Ensure the device is correctly implanted following the manufacturer's guidelines.
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Monitor the patient post-surgery for any signs of device failure or complications.
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Fully inform patients about potential risks and alternative treatments.
Failure to fulfill these responsibilities could lead to medical malpractice claims, holding healthcare providers accountable for negligence in addition to the liability of the device manufacturer.
Steps to Take if You Are Affected
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Seek Medical Attention: Your health comes first. If you suspect your device is malfunctioning, consult your doctor immediately.
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Preserve Evidence: Keep all medical records, device packaging, and communications related to the device.
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Check for Recalls: The FDA maintains a database of recalled medical devices. A recall can support your case.
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Consult with a Personal Injury Lawyer: An experienced attorney can evaluate your case and guide you through the legal process.
How Dordick Law Can Help
At Dordick Law, we specialize in personal injury cases, including those involving defective medical devices. With decades of experience, we are committed to holding manufacturers accountable and securing justice for victims. If you or a loved one has suffered due to a defective medical device used in heart surgery, contact us by clicking here or call us toll-free (800) 555-5595.
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