September 2017

Signs your hip replacement device is failing

Hip replacement devices are meant to improve your quality of life, not make it worse. For many, hip replacement surgery does not end well. Not long after going through recovery patients notice issued with their replacement device. Here are the common signs that show possible hip replacement device failure in Tennessee.

The most common signs that your hip replacement is failing include the following:

  • A feeling that the hip joint has become dislocated
  • Pain when moving or walking
  • Lumps near the hip where the device is installed
  • Swelling in the groin area or on the hip
  • Popping or squeaking noises when walking

You can also determine if your hip replacement is failing by having a blood test performed. A doctor will test your blood for abnormal levels of cobalt or chromium in your bloodstream. If there are elevated levels of these, it’s possible that the replacement hip is wearing down. You could suffer from blurry vision, organ damage and dizziness if these elevated levels are found.

Other tests that doctors can perform to determine if your hip replacement is failing include an MRI, an ultrasound and a physical assessment. Even if you have not experienced any pain or symptoms, you should be evaluated regularly if you have received a hip replacement. Regular evaluation will help discover any issues that could be present.

Has your hip replacement device failed? If so, visit our site to learn about defective medical devices in Kingsport and how an experienced attorney can help your case move forward in the legal system.

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Key factors in a defective medical device claim

Medical devices should assist individuals with living better lives, but what happens when they cause further injury or impairment? In such instances, it may be possible to file a defective medical device claim.

If you or a loved one faces injuries due to a defective medical device, you deserve just compensation. Make sure that you build the best case possible by understanding a few key factors in any defective medical device claim.

Classification

Some cases teeter the line between a defective medical device case and a medical malpractice case. It is critical that you know the difference so you may properly classify your claim. In short, a defective medical device is a device with a design or manufacturing defect. If a device does not denote proper warnings about side effects or risks, it may receive a defective classification as well. On the other hand, if the injury is due to the improper use or placement of the device, it may be a medical malpractice case.

Regulation

The FDA regulates medical device safety. The organization provides standards and procedures with which companies must comply. If a party can show that a manufacturer did not follow the FDA guidelines and stipulations, it may greatly benefit the case. However, even if a company does abide by the FDA’s rules, it does not get them completely off the hook either. Working with a knowledgeable attorney may help you in building a solid case no matter where the manufacturer or seller stands.

Statute of limitations

As with a regular personal injury case, individuals must file their claims within a set time limit according to the state’s statute of limitations. However, considering that individuals may not be aware of the injury right away, Tennessee applies the discovery rule, which generally states that the time limit does not begin until the individual becomes aware of the injury or illness.

These are just a few of the key factors in a defective medical device claim. If you are considering such a case, take some time to fully understand the process and determine the best route for you.

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