Posts Tagged ‘Glens Falls’
Network Zimmer Hip Replacement Lawyer Win $2 Million Against Zimmer Hip ReplacementDo You Have A Faulty Zimmer M/L Taper Hip Prothesis With Connective Technology and Cobalt Chromium Head?
Do You Have Have Metallosis or Chromium Cobalt Toxicity?A judge in Florida has found that Zimmer Orthopedics manufactured and marketed a hip replacement implant which has an “unreasonably dangerous design,” and has ordered the company to pay a victim $2 million.
Zimmer Hip Replacement LawyersWe are proud to say that the $2 million award against Zimmer was won by a member of our lawyer network in co counsel with another attorney.
Testing Inadequate To Substantiate SafetyThe testing done by Zimmer for this prothesis hip implant was inadequate to substantiate safety for the recipient.
Get a Zimmer Hip Replacement Lawyer NowIf you have a faulty Zimmer hip replacement or have high levels of chromium or cobalt in your blood stream contact us immediately for a Zimmer Hip Replacement lawyer. Zimmer Hip replacement lawyers are being filed for victims of the faulty hip replacement and people with metallosis ( Metal Toxicity ) in: we have attorneys in: Auburn AL; Birmingham AL; Dothan AL; Gadsden AL; Huntsville AL; Mobile AL; Montgomery AL; Muscle Shoals AL; Tuscaloosa AL; Anchorage AK; Fairbanks AK; Juneau AK; Flagstaff AZ; Sedona AZ; Mohave County AZ; Phoenix AZ; Prescott AZ; Show Low AZ; Sierra Vista AZ; Tucson AZ; Yuma AZ; Fayetteville AR; Fort Smith AR; Jonesboro AR; Little Rock AR; Bakersfield CA; Chico CA; Fresno CA; Humboldt County CA; Inland Empire CA; Long Beach CA; Los Angeles CA; Mendocino (new) CA; Merced CA; Modesto CA; Monterey CA; O.C. 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Do You Want To File A Talcum Powder Lawsuit?If you have used talcum powder or baby powder products and developed ovarian cancer you may be able to file a Talcum Powder lawsuit Current lawsuits Johnson & Johnson claim that long-term use of talc-based products caused women to develop ovarian cancer. Victims claim that they were not warned of the risks associated with these talc products. Women and their families may be able to seek compensation for ovarian cancer diagnosis with the help of one of our lawyers.
Is There A Risk of Talcum Powder Causing Ovarian Cancer?Talcum powder lawsuits claim Talcum Powder caused ovarian cancer. When used as a feminine hygiene product, talc particles can travel through the vagina and into the ovaries and remain trapped for years. These talc particles can cause inflammation and eventually lead to the growth of ovarian cancer cells.
Studies Claim Dangers Of Talcum PowderAlthough Johnson & Johnson maintains that talcum powder is safe for use, plaintiffs in ovarian cancer lawsuits offer studies that suggest an association between talc and ovarian cancer dating as far back as 1971. In 1994, Johnson & Johnson was put on notice of a link between talc and ovarian cancer. A letter was sent from the Cancer Prevention Coalition to the then-CEO of the company.
Will There Be a Talcum Powder Ovarian Cancer Class Action Lawsuit I Can Join ?According to news reports, more than 1,200 women claim talcum powder caused their ovarian cancer. Currently the lawsuits are being filed at the state level.
Talcum Powder Lawsuit SettlementsA $72 million talcum powder verdict is handed down against Johnson & Johnson in favor of a woman who claimed that long-term Shower-to-Shower use for feminine hygiene caused her to develop ovarian cancer. The verdict included a $62 million award of punitive damages against the company. Our talcum powder cancer lawyers are available to discuss your options.
Benicar Gastrointestinal Injury Lawyers
Filing Benicar Intestinal Injury Lawsuits
What Is Benicar?Benicar is a high blood pressure medication. Benicor has been linked to severe intestinal injury, intestinal damage, chronic diarrhea, malnourishment and severe weight loss. Seniors are the largest population receiving prescriptions for Benicar and are the most vulnerable to sever injury from Benicar.
FDA Benicar WarningsThe FDA has warned patients and doctors that Benicar (olmesartan medoxomil) may cause a severe gastrointestinal (GI) problem called Villous Atrophy. Benicar causes the intestines to lose the texture and makes it difficult to absorb nutrients. This leads to malnutrition which and other digestive problems. This is very dangerous for seniors and can lead to death or hospitalization because of dehydration, chronic diarrhea and malnutrition. Villous Atrophy can result in limiting the ability of the small intestines to absorb nutrients from food. At the most serious stages, villous atrophy causes damage to the intestinal crypts, which is the intestinal lining that surround the villi.
Benicar Villous Atrophy Lawyers Filing Benicar LawsuitsBenicar has been used by millions of people. Benicar warnings did not adequately disclose how serious the side effects form this medication is. The Benicar lawyers at Class Action Lawyer Network are filing claims for individuals who have experienced chronic diarrhea, sprue-like enteropathy or villous atrophy after using Benicar.
Hemorrhages Caused by Xarelto
Xarelto Lawyers Filing Extensive Bleeding LawsuitsOur Xarelto lawyers are accepting Xarelto lawsuits for hemorrhage caused by Xarelto. Nationwide Xarelto attorneys are reviewing cases of excessive bleeding from Xarelto. In a recent Xareleto lawsuit a widow from Missouri has filed an Xarelto claim against Johnson & Johnson, Janssen Research & Development, Bayer Healthcare Pharmaceuticals, et al. to demand that the defendants be held liable for the death of her husband. Dixie A. Smith, surviving spouse of Jay Christopher Smith, filed the complaint in the U.S. District Court for the Eastern District of Louisiana, where it joins similar lawsuits pending in multidistrict litigation (MDL) No. 2592 before Judge Fallon. The plaintiff contends that had her late husband never taken the defendants’ medication, Xarelto, he would not have suffered a deadly intracerebral hemorrhage. Ms. Smith is suing for compensatory damages for past, present, and future economic expenditures incurred as a result of the decedent’s use of Xarelto, including medical and funeral expenses, loss of earnings, loss of companionship and support, and loss of the prospective net accumulations of an estate. Xarelto Caused A Brain Hemorrhage The decedent’s physician prescribed Xarelto (rivaroxaban) during December of 2012. He continued to take the medication as prescribed until May of 2013. On May 4, the decedent was admitted to an intensive care unit (ICU), at which point the hospital staff discontinued his use of Xarelto. He was transferred to the care of a specialty hospital unit on May 18 and on May 22 he died of the intracerebral hemorrhage. According to Ms. Smith’s Xarelto lawsuit, her late husband’s passing was a direct result of his use of rivaroxaban, which he reportedly never would have taken had he been fully informed of the risks. Xarelto is an anticoagulant or blood thinner that is prescribed for the treatment and prevention of blood clots. The medication is intended to reduce the risk of life-threatening complications caused by blood clots, including pulmonary embolism and stroke. Xarelto Lawsuits The product liability lawsuit regarding Xarelto draws attention to several reviews and clinical studies of the drug, including a 2012 report issued by The Institute for Safe Medication Practices. This report stated that there had been “356 reports of serious, disabling, or fatal injury in which rivaroxaban was the primary suspect drug. The report more than doubled from the previous quarter total of 128 cases.” The organization brought these statistics to the attention of the defendants, who reportedly advised The Institute for Safe Medication Practices that the data did not reflect any safety issues that required action. Ms. Smith’s Xarelto lawsuit alleges that the defendants prioritized profit over patient safety. Her complaint further claims that the defendants concealed their knowledge of the severe and life-threatening complications of Xarelto from consumers and the medical community. The lawsuit notes that the pharmaceutical giants failed to highlight the risks of uncontrollable bleeding events, nor did they provide medical protocols for stabilizing patients suffering from these bleeding events. Xarelto had been marketed as a replacement for an older blood thinner, warfarin (Coumadin). Warfarin has been used for years for patients who may be at a higher risk of blood clots. However, patients taking warfarin required regular medical monitoring and dietary restrictions, which Xarelto had promised to eliminate. Our Xarelto lawyers have been reviewing claims for excessive bleeding like these. Xarelto lawsuits are now consolidated in an MDL because many people have suffered injuries of a same type from Xarelto. Speak to an Xarelto lawyer today.
Lawyers Filing Ovarian Cancer Lawsuits For Baby Powder
Talcum Powder Ovarian Cancer Lawsuits Do You Want To File A Baby Powder Cancer Lawsuit?Studies show that talcum-based powder can cause ovarian cancer in women who have used it for genital/perineal hygiene. Studies dating back to 1982 have consistently linked prolonged talc-based baby and body powder usage with ovarian cancer. The talc particles moves through the female reproductive system and settles in the ovaries. These particles may remain in the ovaries for many years, creating inflammation resulting in the development and proliferation of cancer cells. Studies HAVE Linked Ovarian Cancer to Talc-Based Baby/Body Powder The pathology reports and tissue samples that were used to diagnose the ovarian cancer can now be examined to determine whether your ovarian tissues contain talc particles. Talc particles can be found in the pelvic lymph nodes, ovaries, and fallopian tubes and take many years to disintegrate and exit the body. The talcum powder cancer lawyers at Class Action Lawyer Network are speaking to women about talc having caused your ovarian cancer.
Speak To A Talcum Powder LawyerIf you have been diagnosed with ovarian cancer after long term use of talcum-based products, such as Johnson & Johnson Baby Powder, Shower to Shower, and others we want to talk to you regarding filing a talcum powder cancer lawsuit.
Injured In An Accident Due To The Faulty GM Ignition Switch?
GM is facing at least 15 federal lawsuits in relation to the recalled faulty ignition switch.
GM Class Action Lawyers Filing Lawsuits
GM has admitted to knowing of the defect in 2001
This is well over a decade before the recall was even announced.
GM did not give drivers safety warnings
They merely recommended using the ignition key with no keychain or other keys on the keyring.
Can I File GM Ignition Switch Lawsuit?
Class Action Lawyer Network GM Ignition lawyers are accepting injury cases if you or somebody you know has been injured by the faulty GM ignition switch.
Time to File Depends on the Date of Injury
Statutes of limitations are state laws that require plaintiffs to file their cases within set time periods. Because all defective medical device lawsuits are tort claims, they are covered by state law and not federal law. Any medical device lawsuits before U.S. District Courts are claims brought under state law by plaintiffs from states other than the ones in which the manufacturers are located. The purpose of statutes of limitations is to encourage injured parties to bring their claims in a timely manner to prevent courts from dealing with old records and hazy memories.
The amount of time a statute of limitations gives someone to file a claim depends on the type of claim the plaintiff is filing. Commonly, the limitations period for products liability cases is two or three years from the date of injury. When the injury occurred matters significantly from a legal standpoint. Sometimes, the injury “occurs” the day the vaginal mesh was implanted; other times it “occurs” when the plaintiff first knew or could have reasonably found out about the injury. This can be troubling for vaginal mesh recipients because the pain and symptoms of mesh erosion might not occur until long after the initial procedure. Because some women might have already had their vaginal mesh problems resolved years ago and didn’t meet with a Vaginal mesh lawyer, the statute of limitations might have already expired for them, and they will be unable to obtain compensation via a transvaginal mesh lawsuit. If you are having complications ffrom a vaginal mesh it is in your best interests not to wait and file with a lawyer immediately. You must not run the risk of losing your rights to file a lawsuit. The vaginal mesh complications are sever and the mesh implants are ruining lives. You Must send a message and contact a lawyer today. 1 877 522-2123
More than 150 federal lawsuits involving vaginal mesh slings were consolidated in a U.S. District Court in West Virginia. "actions in each MDL share factual issues arising from allegations of defects in pelvic surgical mesh products manufactured by AMS, Boston Scientific, and Ethicon." The cases will be heard in front of one judge who understands the issues.
Ask Questions Get Answers
Also known as a pelvic sling, bladder mesh, or transvaginal mesh, the vaginal mesh support systems are used to help with pelvic organ prolapse as well as urinary incontinence It is now known that they can cause serious internal injuries. These vaginal mesh patch implants, manufactured by Johnson & Johnson , C.R. Bard, Boston Scientific, American Medical Systems, and others, may cause pain, infection, erosion, organ damage, and additional surgeries, and other vaginal mesh injuries.
If you have experienced vaginal mesh complications following pelvic organ prolapse surgery or stress urinary incontinence surgery, The vaginal mesh Helpline will offer support and direct you to a lawyer who may be able to help you obtain significant compensation for the vaginal mesh problems you are experiencing.
Call us at 1 877 -522-2123 to speak with a female social worker and be directed to a lawyer.
Vaginal Mesh- History of the Problem
Between the years of 2005 and 2010, nearly 4,000 vaginal mesh injuries have been reported to the Food and Drug Administration. In a 2010 article in the journal Obstetrics & Gynecology, researchers stated that they had to cease a vaginal mesh clinical trial early because of the higher-than-expected number of complications and injuries. The trial was stopped when it was discovered that more than 15 percent of women who were implanted with vaginal mesh suffered vaginal mesh erosion within only three months of implantation. As a result of numerous negative reports, the FDA issued a vaginal mesh warning to patients and physicians in 2011, cautioning that the risks of using vaginal mesh are so severe that alternative treatments should be considered. It is now widely accepted that, in most cases, pelvic organ prolapsed can be treated without the use of vaginal mesh
What are the vaginal Mesh Injuries
Erosion of vaginal tissue
Hardening of the vaginal mesh
Pain and discomfort
Perforations of the bowel, bladder or blood vessels
Recurrence of Pelvic Organ Prolapse (POP) and Stress Urinary Incontinence (SUI)
Vaginal mesh erosion
Many women who have suffered injuries as a result of vaginal mesh have decided to file defective medical device lawsuits. This has become a class and class action lawsuits are being filed. An product liability, class action attorney can review your case.
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If you have suffered any of the above listed injuries after being implanted with vaginal mesh to remedy a pelvic organ prolapse or urinary incontinence you may be entitled to compensation in a dangerous medical device class action litigation. An experienced medical product liability Attorney will analyze your claim and explain your legal rights. Speak to A female MSW about your vaginal mesh .