Stryker Hip Settlement Alert for Baltimore, Maryland Residents - there has been a 1.4 billion dollar settlement in the Stryker Hip Implant MDL. Please take the time to get fully informed about the Stryker Master Settlement Agreement.
Potential Dangers of the DePuy Pinnacle Hip: There are a number of very serious potential dangers associated with the DePuy Pinnacle hip, including metallosis, metal poisoning, ALVAL, the development of pseudo-tumors and synovitis. Synovitis is similar in nature to metallosis, however it affects the lining of the joint, causing serious inflammation. Some patients may experience few symptoms, while others may notice their hip joint feels “puffy” and warm to the touch due to the increased amount of blood flow. Those with a DePuy Pinnacle hip implant should have regular MRIs in order to identify implants with a high probability of failure.
Synovitis frequently has no adverse health symptoms and is only identified with an MRI. DePuy Pinnacle hip dangers can also include the development of pseudo-tumors which are usually non-infectious, space-occupying tumors which are most often non-cancerous. Netherlands research found that those with metal hip implants had four times the risk of developing pseudo-tumors, and those with any sensitivity to heavy metals have an even higher risk.
What Led to the DePuy ASR Hip Recall? The DePuy ASR hip recall occurred in August, 2010. While the ASR received FDA approval based on its similarity to the Pinnacle model, the Pinnacle has not been recalled. The DePuy ASR is considered by many to represent one of the biggest medical device failures in recent decades. The DePuy lawsuits may shed some light on what DePuy officials actually knew about the potential problems related to the ASR prior to the DePuy ASR hip recall. It is estimated that more than 100,000 ASR implants were sold, and that between 2008 and 2010, at the time of the recall, more than 400 adverse event reports were sent to the FDA.
Do You Have Symptoms of Stryker ABGII Hip Metal Blood Poisoning? If you are the recipient of a Stryker ABGII hip implant, you may have suffered symptoms of Stryker ABGII hip metal blood poisoning. This can occur when the tiny cobalt and chromium ions shear away from the components of the hip implant, making their way to the bloodstream. There are many different symptoms associated with Stryker ABGII hip metal blood poisoning, including the following:
- Disruption of DNA and the inability of the body to repair DNA
- Hypersensitivity and inflammation in the hip region
- Liver necrosis caused by high levels of chromium
- Renal impairment
- Reproductive disorders
- Loss of hearing and vision
- Asthma and other respiratory disorders
- Skin rashes
- Nerve impairment
- The development of pseudo-tumors
- Neurological and cardiovascular disorders
- Gastrointestinal disorders
- Irritability, depression, anxiety
- Short term memory loss
- Vertigo
What to Do When You Suffer From Stryker ABGII Hip Metallosis: When the heavy metal ions land in the surrounding hip tissues, you may be subject to symptoms of Stryker ABGII hip metallosis which leads to severe inflammation, pain in the hip, thigh and groin areas, deterioration and death of bone and tissue, the necessity of revision surgery and total hip failure. Metallosis is also known as aseptic fibrosis or local necrosis. When the metal surfaces of the hip components rub against one another during periods of activity, corrosion, fretting and excess wear can occur. This leads to the shearing away of tiny metal ions from the components; this metal debris can accumulate in the soft tissues of the body, leading to Stryker ABGII hip metallosis.
Are You Affected By the Baltimore, Maryland Stryker ABGII Hip Statute of Limitations? All states operate under the statutes of limitations regarding product liability cases, with most states having a two-year statute. In the state of Maryland, action must be brought within three years from the date you were injured. Determining this exact date can be difficult, however. Perhaps you realized your Stryker ABGII had made you sick, or maybe you knew you were sick but did not associate your symptoms with your recalled Stryker ABGII. The best way to receive competent advice regarding the Baltimore, Maryland Stryker ABGII hip statute of limitations is to consult with a qualified Baltimore, Maryland hip metallosis attorney.
Where the Baltimore, Maryland Hip Metallosis Litigation Stands: DePuy and its parent company, Johnson & Johnson, had more than 11,000 ASR lawsuits filed against them and more than 5,400 Pinnacle lawsuits. Johnson & Johnson settled approximately 7,000 of the ASR lawsuits for $2.5 billion. The Stryker Rejuvenate and ABGII recall resulted in more than 2.300 lawsuits, with more expected as the statutes of limitations grows near for those in some states. Only seventeen of the Rejuvenate/ABGII have been settled thus far for an undisclosed amount; the remainder are being set for mediation and bellwether trials, although many believe Stryker will follow the lead of Johnson & Johnson and settle at least a portion of the lawsuits.
Speaking to a Baltimore, Maryland Hip Recall Attorney: If you have been injured by a Stryker Rejuvenate or ABGII, a DePuy ASR or Pinnacle, or a Biomet M2A MAgnum, Smith & Nephew R3, Wright Systems Conserve THS / Profemur or Zimmer Durom, you may be entitled to pursue compensation for your injuries. A well qualified Baltimore, Maryland hip metallosis lawyer may be able to help.