Dangerous Medical Devices

    FDA Approval? What Does that Mean?

    Medical devices and implants undergo strict government testing before they’re approved for market. Medical companies often try to hide behind FDA approval to deny liability if one of their products causes injury, but the courts are changing. If you’ve been injured because of a failed implant or a dangerous medical device, you’re entitled to seek money damages, even if the Food and Drug Administration have approved the product.

    No Attorney Fees Unless We Help You Recover Money

    Shamberg, Johnson & Bergman is one of the leading defective product litigation firms in the Midwest. Since 1949, we’ve helped thousands of negligence victims recover full and fair money damages after an injury or wrongful death. We’ve also earned recognition for providing intelligent and successful representation.

    The U.S. Food and Drug Administration* currently lists more than 120 dangerous medical devices that have been recalled from the market since 2001. Some of these recalled products include:

    • Implantable infusion pumps and power packs
    • Pacemakers
    • Automatic external defibrillators
    • Catheters and coronary stents
    • Implantable ventricular assist devices
    • Blood glucose monitoring systems and test strips
    • Continuous renal replacement systems

    Recall information

    Free Consultation

    Contact our dangerous medical device lawyers to learn more about our record of success. Our experienced trial attorneys represent clients in cases throughout Missouri, Kansas and the Midwest. You can also call us toll free at 866-484-8966 to arrange a free consultation. If you can’t come to us, we’ll try our best to come to you.

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