Attention Stryker Hip Implant Recipients from Portland and other locales in Oregon! Stryker Corporation has reached a 1.4 billion dollar settlement agreement in its litigation over its Stryker Rejuvenate and Stryker ABGII metal on metal hip implants. Learn more about the Stryker Hip Settlement here...
Understanding the Portland, Oregon Stryker Hip Statute of Limitations
If you have a Stryker Rejuvenate or Stryker ABGII hip implant, you have likely heard of the main issues associated with metal-on-metal hip implants. You may also wonder just how the Portland, Oregon Stryker hip statute of limitations may affect you. All states have statutes of limitations which limit the amount of time you are allowed in which to file a product liability cases such as one for a dangerous medical device. The state of Oregon—like many other states—allows two years from the date your injury occurs to file such a case.
Oregon also has an eight-year statute of repose; the statute of repose is triggered by an event such as the date of the sale or the date of the manufacture of the device. Both the Portland, Oregon Stryker hip statute of limitations and the Oregon statute of repose can be complex and difficult for most laypeople to understand. For this reason it could be beneficial for you to speak to a Portland, Oregon hip metallosis lawyer in order to properly determine exactly how much time you have to file a claim.
What Causes Stryker Rejuvenate / ABGII Hip Metal Debris?
Before 1976, the FDA had no control over medical devices such as hip implants, and a number of metal hip devices were marketed in the U.S. despite documented concerns regarding the potential toxicity of cobalt and chromium ions in the body. In 1976 the FDA placed metal hip implants under FDA regulation. At that time these metal hip implants were still being classified as a Class III device, meaning there was significant risk attached to the device. Even so, the FDA allowed fast-track 510(k) approval of metal hip implants, with few or no clinical trials required.
Many manufacturers jumped on the metal hip implant bandwagon, claiming the devices were perfect for the younger, more active patient, would last longer, and were completely safe. One of the primary complications of the Stryker Rejuvenate and ABGII metal hip devices is generation of Stryker Rejuvenate / ABGII hip metal debris. When a patient is active, the metal components rub against one another, releasing tiny metal ions into the bloodstream and into hip tissues. The cobalt and chromium ions which enter the bloodstream can result in Stryker Rejuvenate / ABGII hip chromium and cobalt metal poisoning, while the metal shards which lodge in the hip tissues can be responsible for Stryker Rejuvenate / ABGII hip metallosis.
The Many Metal on Metal Hip Dangers
There are many DePuy Pinnacle hip dangers, DePuy ASR hip dangers, Stryker Rejuvenate hip dangers and Styryker ABGII hip dangers. Metallosis is one of the more serious dangers associated with metal hip devices. When metallic debris begins to accumulate in the body’s soft tissues, hip metallosis can result. The symptoms of metallosis include pain in the groin, hip or thigh, inflammation, deterioration of bone and tissue, loosening of the implant and the necessity for the patient to undergo hip revision surgery.
Synovitis, ALVAL and the development of pseudo-tumors can also result from the buildup of cobalt and chromium in the body. Synovitis is similar to hip metallosis, but is limited to inflammation of the joint lining. This type of inflammation can occur long before the patient is aware of overt symptoms. Among some people the joint may swell, feeling puffy or warm to the touch. An MRI is the best way to detect the presence of synovitis.
When cobalt and chromium ions enter the bloodstream, the body will attempt to excrete the heavy metals through the liver and kidneys. As the metal ions continue to accumulate, it becomes more and more difficult for the body to do so. Metal Hip chromium and cobalt poisoning can cause such serious symptoms as: gastrointestinal, renal, thyroid, reproductive, cardiovascular and neurological disorders, loss of hearing and vision, tremors, vertigo, depression, anxiety, asthma, skin rashes, the development of pseudo-tumors, DNA disruption, seizures, chronic headaches and extreme fatigue.
Were You Affected by the DePuy ASR Hip Recall or the Stryker Rejuvenate / ABGII Hip Recalls?
If you were affected by the DePuy ASR hip recall, the Stryker Rejuvenate hip recall, or the Stryker ABGII hip recall, it could be beneficial for you to speak to a Portland, Oregon hip metallosis lawyer in order to ensure your rights are protected and your lawsuit is filed in a timely manner.
You may be wondering what the status of Portland, Oregon hip metallosis litigation is at this time...
Following the Stryker Rejuvenate and ABGII recalls, over 2,300 lawsuits were filed against that company. Following the DePuy ASR hip recall, more than 11,000 lawsuits were filed, however approximately 7,000 of those were settled for $2.5 billion. There are currently over 5,000 DePuy Pinnacle lawsuits pending as well. If you believe you are entitled to file a Portland, Oregon Stryker Rejuvenate / ABGII hip metallosis lawsuit (or any other metal hip lawsuit), contact a Portland, Oregon hip metallosis attorney to evaluate your case.