Hip Metallosis Lawyers & Lawsuits: Indianapolis, Indiana

Stryker Hip Settlement Alert for Indianapolis, Indiana 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.


Were You Affected by the DePuy ASR Hip Recall? The DePuy ASR hip recall occurred in August, 2010, after more than 400 adverse event reports were received by the FDA regarding the metal hip implant. Metal on metal hip implants like the ASR—in which the cup and ball of the device are both made of metal—accounted for one in three hip implants used in the U.S. just a few short years ago. Today, after the many health problems suffered by implant recipients, these types of metal hip implants account for less than ten percent of the total.

It is estimated that more than 100,000 ASR hip devices were implanted between FDA approval of the device and the DePuy ASR hip recall. The ASR gained FDA approval in 2005 under the 510(k) process, claiming it was substantially similar to the already-released Pinnacle. Problems appeared with the ASR as early as 2006, particularly among women, and those with weaker bones, and Australian officials discontinued sales of the implant a full year prior to the U.S. recall. 

Understanding Stryker ABGII Hip Dangers: Like the DePuy ASR, the Stryker ABGII gained FDA approval through the 510(k) process, claiming they were substantially similar to the Wright ProFemur metal hip implant which, according to the Australian National Joint Registry, has a revision rate several times that of comparable hips. The FDA database notes that Stryker experienced problems with the ABGII for some time prior to the recall in July, 2012. Only six months after the ABGII was marketed, one surgeon removed an ABGII from a patient, noting significant levels of fretting and corrosion.

Later, in 2011, another surgeon noted the presence of what appeared to be black rust on a Stryker implant removed from a patient. In 2010 alone, the FDA received over 60 adverse event reports; by the end of 2011 that number had risen to 130 and by the time of the recall the adverse event reports had reached 300. Stryker ABGII hip dangers include metallosis, metal poisoning, synovitis, ALVAL and the development of pseudo-tumors.

Symptoms of Stryker ABGII Hip Chromium and Cobalt Poisoning: Patients who have suffered a buildup of heavy metals in the bloodstream can suffer symptoms of Stryker ABGII hip chromium and cobalt poisoning. Some of these symptoms include the loss of hearing and vision, gastrointestinal disorders, renal, thyroid, neurological and cardiovascular disorders, anxiety, depression, irritability, tremors, muscle spasms, asthma, skin rashes, reproductive disorders, the development of pseudo-tumors and changes in DNA. Even after the metal hip implant is removed through Stryker ABGII hip revision surgery, you may still suffer symptoms of Stryker ABGII hip chromium and cobalt poisoning. Stryker ABGII hip metallosis can lead to chronic pain in the hip, thigh and groin, inflammation, deterioration of tissue and bone, hip failure and the necessity for revision surgery.

Will You Be Forced to Undergo Stryker Rejuvenate Hip Revision Surgery? If your surgeon determines that your Stryker Rejuvenate hip has failed or that your symptoms of metallosis or metal poisoning are severe, you may have to undergo Stryker Rejuvenate hip revision surgery. The stem of the Stryker Rejuvenate is especially long, which means it is implanted deeply within the femur. During Stryker Rejuvenate hip revision surgery the surgeon must dig the stem out of the femur, and, in some cases, the femur can shatter during the operation. The surgery is considered riskier than the original implantation surgery, as the patient may be on the operating table as long as four to six hours, leaving them exposed to excessive blood loss, infection and nerve damage. The recovery period of Stryker Rejuvenate hip revision surgery can be as long as six weeks, meaning you could be off work for a significant period of time.

How the Indianapolis, Indiana DePuy ASR Hip Statute of Limitations May Affect You: If you have suffered injury from a DePuy ASR, you must be aware of the Indianapolis, Indiana DePuy ASR hip statute of limitations. Every state operates under statutes of limitations, and the state of Indiana allows two years from the time your injury occurred to file a lawsuit against the manufacturer. Indiana also has a ten-year statute of repose which is triggered by an event, rather than an injury, such as the date the device was manufactured or sold.The best way to properly and correctly determine exactly how much time you have to file a hip metallosis lawsuit based on your individual circumstances is by speaking with a knowledgeable and skilled Indianapolis, Indiana  hip metallosis lawyer.

Hip Metallosis Lawsuits in Indianapolis, Indiana: If you have been injured by a metal hip implant in Indianapolis, Indiana, you may be entitled to file a hip metallosis lawsuit. You may be eligible to pursue compensation for your injuries, depending on the specific facts surrounding your case. Thus far there have been more than 11,000 DePuy ASR lawsuits, over 5,400 Pinnacle lawsuits and more than 2,300 Stryker Rejuvenate and ABGII lawsuits filed.

DePuy and its parent company, Johnson & Johnson, settled approximately 7,000 of the DePuy ASR lawsuits for $2.5 billion. Stryker settled seventeen Rejuvenate and ABGII lawsuits through mediation, and the remainder are being set for mediation and bellwether trials. The first Pinnacle trial ended in October, resulting in a decision for the defendant. Further trials will be set for all four hip devices, as well as for Biomet M2A Magnum, Smith & Nephew R3, Wright Systems Conserve THS / Profemur, and Zimmer Durom hip devices.

Do You Need an Indianapolis, Indiana Metal on Metal Hip Attorney? Only an experienced Indianapolis, Indiana metal on metal hip attorney can accurately determine when your statute of limitations will run, and whether you have a valid metal hip case. It can be beneficial to consult with an Indianapolis, Indiana hip metallosis attorney who can give you a comprehensive evaluation of your case.

DISCLAIMER: Statutes of Limitations limit the amount of time that an individual has to file a lawsuit, and not only vary from state to state, but also vary by cause of action. The information provided above and in the city/state-specific pages in this section is meant as a general guide, and is for informational purposes only. Each client’s case is unique, and the specific circumstances of any individual case can have significant bearing on the applicable statute of limitations. Any person who believes they may have a viable cause of action is strongly encouraged to consult with an attorney about the statute of limitations for his or her case. Attorney Andrew Sullo is licensed to practice law in Texas, and can prosecute cases that are part of a federal multi-district litigation. Andrew Sullo does not practice law in any other state, and is not certified by the Boards of Legal Specialization in any state. Not all states have board certifications. This information is not intended to solicit clients for matters outside of the State of Texas. Our firm is not accepting cases in any state where it would be impermissible for it to do so. Sullo & Sullo, LLP maintains its principal office in Houston, Texas.

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