Understanding the Stryker Rejuvenate/ABGII Hip Lawsuits
Consumers who underwent hip replacement surgery with a Stryker Rejuvenate/ABGII hip implant are currently filing lawsuits to seek compensation for their losses, including medical expenses, lost wages, loss of future wages, physical pain and emotional trauma. Following the Stryker Rejuvenate/ABGII hip recalls in July, 2012, many injured consumers felt the manufacturer should be held accountable for releasing a defective product into the marketplace. At the time of the recall, Stryker noted the Rejuvenate and ABGII had a higher-than-normal rate of failure and were more likely to cause Stryker Rejuvenate/ABGII hip metallosis and cobalt and chromium blood poisoning. There are currently over 2,300 Stryker Rejuvenate/ABGII hip lawsuits filed, with the majority of those consolidated under Stryker Rejuvenate/ABGII hip multidistrict litigation. Many of the allegations against Stryker include the following:
· Stryker manufactured the Rejuvenate and ABGII as being perfect for the younger, more active patient, claiming the devices were safe and long-lasting
· Stryker failed to properly test the devices
· The Rejuvenate and ABGII can undergo fretting, corrosion and deterioration
· Stryker failed to warn consumers and surgeons about the potential dangers of the device, including heavy metal poisoning and metallosis
· The Rejuvenate and ABGII systems contain both design and manufacturing defects
· The devices can cause severe and permanent destruction of bone and tissue
· Stryker knew or should have known the product was inherently more dangerous than other available hip implants
· Stryker aggressively marketed the two devices without informing consumers of the potential risks
Seventeen of the Stryker Rejuvenate/ABGII hip lawsuits have been settled through mediation, and bellwether cases are currently being chosen to represent larger groups of Stryker plaintiffs. The first bellwether cases are set for the summer of 2015, and other cases are currently involved in the mediation process.
How the Texas Stryker Rejuvenate/ABGII Hip Statute of Limitations May Affect You
All states have a statute of limitations which governs the amount of time consumers have to file a lawsuit against the manufacturer of a defective product. While the statutes differ from state to state, in the state of Texas any civil cause of action for a product liability case must be filed within two years of the time the injury occurs. It is crucial that you speak to a Texas Stryker Rejuvenate/ABGII hip lawyer in order to determine when your statute will run, as it can be much more complicated than it appears on the surface. If you are a resident of any of the following locales—or anywhere in the state of Texas—you are encouraged to contact a Texas Stryker Rejuvenate/ABGII hip lawyer at your earliest possible convenience.
· Houston, Texas
· San Antonio, Texas
· Dallas, Texas
· Austin, Texas
· Fort Worth, Texas
· El Paso, Texas
· Arlington, Texas
· Corpus Christi, Texas
When to Call a Tennessee Stryker Rejuvenate/ABGII Hip Lawyer
Many victims of the Stryker Rejuvenate/ABGII hip recalls developed Stryker Rejuvenate/ABGII hip metallosis which led to symptoms such as chronic pain in the hip, thigh and groin area, severe inflammation in the hip region, deterioration of tissue and bone, total hip failure and the necessity for the patient to undergo Stryker hip revision surgery. Those who develop cobalt and chromium metal poisoning can experience such symptoms as: gastrointestinal, renal, thyroid, cardiovascular and neurological disorders, DNA disruptions, irritability, depression, anxiety, reproductive disorders, loss of hearing and vision, the development of pseudotumors, skin rashes and loss of memory. If you have experienced any of these or other Stryker-related injuries, you should strongly consider speaking to a Texas Stryker Rejuvenate/ABGII hip lawyer regarding filing a Texas Stryker Rejuvenate/ABGII hip lawsuit.