Posts Tagged ‘Port st Lucie’
Hip Replacement LawsuitsMany of the Hip replacement manufacturers of the metal-on-metal hip implants have recalled their implants for functional defects. There have been settlement offers on hip replacements for victims of a faulty hip implant or cobalt and chromium poisoning to the blood stream.
Hip Replacement Revision Surgery LawsuitsHip replacement or revision surgery is one of the most common orthopedic procedures performed in the United States. There have been numerous defective implants placed on the market resulting in needles pain, suffering and revision surgeries
Get A Hip Replacement Lawyer
Below is a list of cases our hip replacement lawyers will take a look at.
- Stryker Rejuvenate Modular Neck Cases – All
- Stryker ABG II Modular neck Cases – All
- Stryker Accolade (TMZF) Stem cases with Cobalt Chromium modular heads. These stems have the potential for significant head neck corrosion – All cases with Metallosis.
- Wright Medical Conserve Cup (MOM) cases – ALL
- Wright Medical Profemur Stem Cases (this is their modular neck design)- These cases are prone to Fracture (either the titanium or CoCr necks) and Metallosis. ALL.
- Depuy ASR – ALL
- Depuy Pinnacle Metal on Metal (MOM) with modular heads greater than 36 mm.
- Zimmer Durom Cup cases with modular heads greater than 36 mm.
- Zimmer M/L Taper Kinectiv Stem cases (this is their Modular neck design)- All cases with Metallosis.
- Biomet M2A 38mm / Magnum MOM cases. ALL cases with Metallosis.
- DJO / Encore MOM hip cases. All cases revised due to Metallosis.
- Omnilife Apex Arc – This is a smaller manufacturer but this device is a mixed metal modular neck device. ALL
- Smith & Nephew R3 (MOM) cup cases. Only cases that have metallosis and were revised or need a revision.
- Smith & Nephew SMF stem (this is their mixed metal modular neck product). We have not seen many of these yet but, our hip replacement lawyers are interested in them.
IVC Filter Lawyers Advise – Bard IVC Filter Lawsuits ConsolidatedBard IVC Filter lawsuits have been transferred to a federal court in Arizona. IVC Filter lawyers of Class Action Lawyer Network will help victims injured by the defective IVC filters.
IVC Filter MDLA transfer order filed Monday, in the U.S. Judicial Panel on Multidistrict Litigation (JPML), resulted in all present and future federal product liability lawsuits against inferior vena cava filter (IVC filter) manufacturers, C.R. Bard, Inc. and Bard Peripheral Vascular, Inc. (BPV), to be centralized in a multidistrict litigation (MDL) in the District of Arizona.
What Are IVC Filters?IVC filters are surgical implants that catch blood clots before they travel to the lungs to avoid causing a pulmonary embolism. The Bard IVC Filter devices are fracturing, tilting, migrating, or puncturing the vena cava.
FDA Vena Cava Filter WarningsThe U.S. Food and Drug Administration issued a safety warning in 2010, citing that more than 900 IVC Filter adverse event reports were filed over five years A study published in the April 2013 edition of Jama Internal Medicine, found that less than 10% of retrievable IVC filters surveyed were successfully removed. They also reported that 8% of persons surveyed still suffered venous thrombotic events while the IVC filter was in place. In 2014, the FDA issued an updated warning to doctors recommending that IVC filters be removed within one to two months once the need for the filter has passed. They noted that doctors may not have previously been made aware of the urgency surrounding retrieval of the device.
IVC Filter LawyersIVC filter lawyers will help you get compensation as part of the Bard IVC filter MDL, which has been consolidated to the U.S. District Court of Arizona.
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.
It has become apparent that there is a large number of drugs and devices class actions that have been filed against manyfacturers that have targeted women.
We can start with the Dow Corning siicone breast implant class action of years ago. Women are still suffering today. The Dow Corning Trust just recently launched a silicone breast implant explant program. The leaking silicone and bursting implants lead to toxicity related immune system diseases like lupus and fibromylagia and other immune deficiency diseases. Women to this date are still suffering from their Dow silicone Breast Implants and the Dow Corning settlement trust is stll living out payments like the new breast explant program.
Fosamax was supposed to cure osteoporosis but ended up causing femur fractures.Then we have Yaz and Yasmine birth control pills. Young women were having their lives altered by pre-mature strokes, pulmonary embolisms, deep vein thrombosis, blood clots and heart attacks. Many girls harmed were barely starting a college life.
History moves along to the metal on metal and metal componednt hip replacements like the DePuy Pinnacle and ASR Hip Replacement and the Stryker Rejuvinate and ABG II Modular Stems. These are a metal on metal hip replacement recalled for their need for revision surgery. These hip replacements failed in women more then men. The smaller frame of a women makes the device more prone to problems in the female structure.
NuvRing has been another disaster for women causing:
blood clots in women
cerebral thrombosis in women
deep vein thrombosis
heart attack in women
retinal thrombosis in women
stroke or cerebral hemorrhage
thrombophlebitis and venous thrombosis with or without embolism
toxic shock syndrome
Fosamax for osteoporosis actually causes what it is prescribed to fix , femur fractures.
Vaginal Mesh Lawsuits
The biggest and most horrific is the the various vaginal mesh devices for urinary incontinence and uterine, bladder and bowel prolapse. This mesh device is made of a Prolene plastic synthetic fiber that has been falling aprt in women. Thousands of women across the country are screaming the horrors of the vaginal mesh and lawsuits are being filed in droves. Women are in severe pain described as razor blades. The mesh has been reported by female victims to be eroding thru the vaginal wall and at times into the bladder and bowel. Women can no longer have sexual intercourse and marriages are falling apart. Women are losing their jobs and cannot work. And then we have the Mirena IUD which has been gravitating our of postion and ending up embedded in the uterus or a nearby organ.
Lives are being ruined and justice must be sought. Lawsuits are the only thing these manufacturers understand.
Lipitor lawyers of Class Action Lawyer Network are filing lawsuits for women who are getting type 2 diabetis from lipitor.
Lipitor is prescribed to lower her cholesterol levels and help decrease the risk of developing cardiovascular disease. However, after using the medication many women are being d diagnosed with type 2 diabetes.
It appears Pfizer knew about the increased risk of diabetes from Lipitor, but failed to provide adequate warnings for women and their doctors.
Lipitor Is Causing Type 2 diabetes in women taking Lipitor
What Is Lipitor?
Lipitor (atorvastatin) is one of the most widely used brand-name medications in the United States. Millions of people take the medication to help lower cholesterol. Pfizer had more than $125 billion in Lipitor sales.
FDA Warning For Lipitor
In February 2012, the FDA required new diabetes warnings for Lipitor. This was due to the increased risk of changes to blood glucose levels.
Lipitor lawyers are filing Lipitor lawsuits
Mullti District Litigation Consolidation For Lipitor Lawsuits
U.S. Judicial Panel on Multidistrict Litigation (JPML) rejected a request filed by Lipitor lawyers to centralize all cases brought in the federal court system. The MDL panel has determined that each of the cases will proceed as individual lawsuits in the U.S. District Court where they were filed.More than half of the pending actions are already consolidated before one judge in the District of South Carolina.
If you or a loved one has been diagnosed with Type II Diabetis after taking Lipitor contact us to speak toa Lipitor lawyer today.
DePuy Hip Replacement Lawsuit Update
DePuy ASR lawsuit claims stemming from the 2010 DePuy hip recall continue to move forward in courts throughout the country . According to documents filed in California’s San Francisco Superior Court on April 25th, a Plaintiff who had been seeking an expedited trial of her DePuy hip lawsuit is voluntarily seeking dismissal of the case. (Tilman v. DePuy Orthopaedics, Inc., et al., No. CGC11508806; Calif. Super. Ct., San Francisco).
This news is particularly interesting as when a case is voluntarily dismissed it is often an indication that the parties have come to an agreement.
DePuy ASR Hip Lawsuits Lawyers Filing DePuy Lawsuits
Court records indicate that there are more than 10,000 DePuy ASR hip lawsuits currently pending in courts throughout the U.S. The DePuy hip recall was announced after the metal-on-metal hip implants were found to be failing in an unacceptably high number of patients. The U.S. Food & Drug Administration (FDA) is now reviewing the safety of all metal hip implants, over fears that the devices can shed dangerous amounts of metal debris into patient’s bodies, leading to premature failure of the hips and other serious complications. In January, the agency proposed a new regulation that would make such devices ineligible for the agency’s 510(k) clearance process, which allowed all-metal hips like the ASR hip to gain FDA approval without first undergoing human clinical trials. The FDA also advised doctors to test metal hip implant patients for elevated metal ion levels if they present with symptoms of a failing hip implant.*
The majority of DePuy hip lawsuits have been filed in a multidistrict litigation now underway in U.S. District Court, Northern District of Ohio. Court records indicate that the first trials in that litigation will begin this September. (In re: DePuy Orthopaedics, Inc. ASR Hip Implant Products Liability Litigation – MDL 2197) Two lawsuits have already gone to trial at the state level, one of which ended with a California Superior Court jury awarding the Plaintiff more than $8 million in damages. (Kransky v. DePuy, BC456086, California Superior Court, Los Angeles County) However, the jury hearing a second trial in Illinois state court found for DePuy. (Strum v. DePuy, 2011-L-9352, Circuit Court of Cook County) According to an April 16th report from The New York Times, documents submitted as evidence in both of those trials indicated that Johnson & Johnson and its DePuy Orthopaedics unit knew that the ASR was flawed years before the recall was announced, but did not disclose this information to the public or the medical community.**
Earlier this month, DePuy Orthopaedics announced it would end sales of metal-on-metal hip implants, citing recent FDA actions and decreased demand for the products, according to the New York Times. The sales suspension includes a metal-on-metal version of the company’s DePuy Pinnacle hip replacement system, which is also the subject of lawsuits.
If you have a faulty DePuy and have had revision surgery or have been told you need revision surgery call and speak to a hip replacement lawyer today.
The following dangrous drugs and devices are appearing in lawyer ads and email blasts across the country.: Vaginal Mesh, Transvaginal Mesh, Pelvic mesh, Surgical mesh, Bladder sling, Stryker Rejuvinate hip replacement, Stryker ABG Modular II Stems, Yaz, and Mesothelioma. The following dangrous drugs and devices are appearing in lawyer ads and email blasts across the country.:
Vaginal Mesh Lawsuits
Women nationwide in the thousands are filing vaginal mesh lawsuits for severe mesh complications. The vaginal mesh lawsuits have been consolidated and the bellwether trials are moving ahead.
Vaginal Mesh Multi District Lawsuit List Consolidated Under Judge Goodwin in West Virginia
MDL – 2325, IN RE: American Medical Systems, Inc., Pelvic Repair System Products Liability Litigation
MDL – 2326 IN RE: Boston Scientific Corp. Pelvic Repair System Products Liability Litigation
MDL – 2327 IN RE: Ethicon, Inc., Pelvic Repair System Products Liability Litigation
MDL – 2387 IN RE: Coloplast Corp. Pelvic Support Systems Products Liability Litigation
TransVaginal Mesh Lawsuits
These are still the same Prolene mesh which is causing severe complication, just unsder another name
Pelvic Mesh Lawsuits
Still the same Prolene mesh and vaginal mesh lawyers, transvaginal mesh lawyers, and pelvic mesh lawyers are filing vaginal mesh lawsuits for all of these
Surgical Mesh Lawsuit, Bladder Sling Lawsuits
Still the same vaginal mesh lawsuit products
Stryker Rejuvinate and ABG Modular II Stems Hip Replacement
Class action Stryker lawsuit lawyers are filing lawsuit for the failed Stryker hip replacement where revision surgery is needed. We suggest you see an orthpedic doctor immediately.
The U.S. Judicial Panel on Multidistrict Litigation is considering forming an MDL to handle the growing number of Stryker lawsuits. Both the Rejuvenate and the ABG II hip implants were recalled in July 2012. This was done due to reports that the implants were causing complications including loosening of the joint, corrosion, and increased risk of inflammation as well as metal toxicity. Many victims of these failed devices have had to undergo revision surgery to remove and replace them long before they reached the end of their expected 15-20 year lifespan. On March 18, 2013, Stryker filed a brief with the JPML, agreeing that coordination of lawsuits involving the recalled devices was appropriate.
Yaz class action lawyers are accepting Yaz cases for blood clots, stroke, pulmonary embolism and untimely death of young women.
As of February 12, 2013, Bayer had reached agreements, without admission of liability, to settle the claims of approximately 4,800 Yaz victims in the U.S. for a total amount of about US$1 billion," according to the annual report.
Bayer also said that it, "is only settling claims in the U.S. for venous clot injuries (deep vein thrombosis or pulmonary embolism) after a case-specific analysis of medical records on a rolling basis. Such injuries are alleged by about 3,200 of the pending unsettled claimants. Bayer will continue to consider the option of settling individual lawsuits in the U.S. on a case-by-case basis.
1000's of hard working citizens are starting to show signs of mesothelioma from asbestos exposure on the job. Class action lawyers for Mesothwlioma victims and their families are here to help you.
GranuFlo and Naturlayte, the Dialyis medications causing immediate cardiac arrest have been consolidated into a Massachusetts MDL. The Fresenius Granuflo and NaturaLyte lawsuits filed in the federal court system will now be consolidated before one Massachusetts’ judge for pretrial proceedings, as part of a multidistrict litigation (MDL).
Class Action Lawyer Network GranuFlo lawyers are filing lawsuits for heart attacks or sudden deaths caused by the use of GranuFlo or NaturaLyte dialysis products during hemodialysis. Victims hearts suddenly stop during or shortly after dialysis treatment involving the use of Granuflo Acid Concentrate or NaturaLyte Liquid Acid Concentrate in dialysis treatment.
It appears Fresenius failed to adequately research the side effects of their dialysate products or warn about the potential risks including the importance of monitoring bicarbonate levels of patients receiving the products to avoid sudden cardiac arrest and death.
Dialysis medication lawyers are accepting immediate cases for injury and wrongful death.