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Physiomesh Hernia Mesh Lawyers

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Ehicon Physiomesh Recall Lawyers

The Physiomesh is a Flexible Composite Hernia  Mesh  used in hernia repair surgery. The Physiomesh is made of a synthetic plastic-like material called polypropylene and is used as a patch to repair the hernia. It is the same exact material used in the Ethicon vaginal mesh that has caused problems in thousands of women.

Physiomesh Complications

  • Need for revision surgery due to mesh failure
  • Recurring hernia due to failure of the Physiomesh
  • Pain after surgery.
  • Recurring hernia in the first 6 months following surgery

Ethicon Physiomesh Lawyers Filing Physiomesh Lawsuits

If you have had a hernia repair surgery using the Ethicon Physiomesh and are experiencing complications contact our Physiomesh lawyers. Lawsuits are being filed against Ethicon Inc. for failure of their Physiomesh.

What Is An Inferior Vena Cava Filter? Can I File An IVC Filter Lawsuit?

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An inferior vena cava filter, IVC filter  or blood clot capture filter is a small cone-shaped surgical implant   that is implanted in the inferior vena cava just below the kidneys. The filter is designed to capture  a blood clot that has broken loose from one of the deep veins in the legs on its way to the heart and lungs. The goal is to stop the clot from causing a stroke or pulmonary embolism. Placing an IVC  filter in the inferior vena cava (IVC) is a way to prevent pulmonary embolism (PE) from a deep vein thrombosis (DVT). This procedure is currently performed under radiologist  guidance thru the  femoral vein or jugular vein.

Inferior Vena Cava Filter Lawsuits

The U.S. Judicial Panel IVC Filters fail to improve Anticoagulant Therapyon Multidistrict Litigation (JPML) has established a single court to consolidate all the Bard IVC filter lawsuits filed against C.R. Bard. All Bard cases will be centralized in the federal court system under one judge in Arizona.

IVC Filter Lawsuit Complications- Commonality Of Injuries For Lawsuits Filed
Device migration
Filter perforation
Filter fracture
Detached device componentsy

These complications must have resulted in significant injury, damage to internal organs or death. IVC Filters are helpful in preventing serious medical problems yet, they can cause serious medical problems. Speak to an IVC Filter lawyer today.

Bard IVC Filter Lawsuit Update | Cook IVC Filter Lawyer

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The federal multi-district litigation panel for the Bard IVC Filters  has appointed a federal judge in Phoenix to oversee the C.R. Bard Inc. (NYSE: BCR) IVC filter consolidated lawsuits for all Bard Inferior Vena Cava filter lawsuits nationwide.

An  IVC filter was designed to capture  blood clots in patients who could not use  blood thinners. Our IVC Filter lawyers are filing defective IVC Filter lawsuits for people injured by a defective IVC Filter. Injuries include those from the fracturing of the filter and parts of the filter migrating and puncturing vital organs.  Faulty IVC filters puncture veins, fracture and migrate to other parts of the body causing injury and even death.

Why Are IVC Filter Lawsuits Being Filed?

IVC filter is problematic because   pieces can break off and thru-out the body and injure  parts of the body or get embedded in the organ tissue. These temporary IVC filters are supposed to be taken out within six months.  Very often the device is not removed in time to prevent complications.

IVC Filter Complications

Deep vein thrombosis
Difficulty in removing the filter
Movement of the entire filter or filter fragments to the heart or lungs
Fracture of the filter
Migration of the filter to another part of the body or vital organ
Perforation of the inferior vena cava
Tilting of the filter

If you or a loved one has been injured by a defective Bard or Cook Ivc Filter contact us to speak to an IVC Filter lawyer.

Blood Clot Filter Lawyers

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An inferior vena cava filter,  IVC filter, blood clot filter is a small cone-shaped device that is surgically implanted in the inferior vena cava just below the kidneys. The filter is designed to capture  a blood clot that has broken loose from one of the deep veins in the legs and capture it  on its way to the heart or lungs.

IVC Filter Lawsuits

Our blood clot filter lawyers are accepting IVC filter cases throughout the United States.The Judicial Panel on Multidistrict Litigation has consolidated Bard IVC filter lawsuits in the District of Arizona and has consolidated Cook Medical IVC filter lawsuits in the Southern District of Indiana. All IVC filter lawsuits will be a part of one of these two multi district litigations.

Particles Of The IVC Filter can fracture and migrate resulting in:

Inferior Vena Cava Perforation
Heart or Lung Perforation
Severe Chest Pain
Severe Shortness of Breath
Hemorrhagic Pericardial Effusion or  Hemorrhage

Speak to an IVC Filter Lawyer Today

Vena Cava Blood Clot Lawyers

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The Bard Vena Cava Filter is implanted in patients to capture blood clots. This is used for patients who cannot tolerate blood thinners. The blood clot is captured to avoid traveling to the barain or lungs and causing a stroke of pulmonary embolism. Recent studies show high rates of IVC filter failures and serious injury to the patient.

Bard Recovery filter,

Bard G2 filter,

Bard G2 Express Filter

The use of an IVC filter may cause the following complications:

IVC Filter migration
IVC Filter fracture
IVC Filter perforation
Tilting of the IVC Filter
The inability to retrieve the IVC Filter
Pulmonary embolism
Compromised respiration
Stroke
Death

The filters have caused serious injury in patients. If you or a loved one has been injured by an IVC Filter contact us to discuss inclusion in the current IVC Filer lawsuits.

IVC Filters such as Bard IVC Filters and Bard G2 IVC Filters have been linked to serious injuries

  • Parts of the device breaking lose
  • Movement or migration of the device through the body
  • Puncture or perforation of organs
  • Device being lodged in the wrong part of
    the body
  • Blockage of blood vessels
  • Device being wedged in the body

Lawyers For Dangerous Drugs

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Zofran Lawyers

Zofran is m anufactured by GlaxoSmithKline. Zofran has been prescribed to expectant mothers to treat morning sickness, but has since been linked to birth defects such as cleft palates and lips and congenital heart defects if taken in the first trimester, The FDA never approved this drug to treat morning sickness. It wwas approved for chemotherapy patients.

Xarelto Lawyers

This is a blood thinner made by Janssen Pharmaceuticals. It has caused severe and uncontrolled bleeding resulting in organ injury and deaths

GranuFlo Lawyers

Granuflo is a product developed by Fresenius Medical Care. It is used during kidney dialysis to neutralize excess acid in a patient’s blood. Granuflo has caused sudden, fatal heart attack and was recalled by the FDA in May 2012.

Januvia Lawyers

Januvia is prescribed for Type II diabetes and made by Merck & Co. It is shown to cause pancreatitis and pancreatic cancer that can lead to death.

Thousands of lawsuits have been filed against the manufacturers of drugs for failing to warn the public and medical community about possible side effects. If you or a loved one has been injured or you have lost a loved one due to these medications speak to one of our drug or devices lawyers today

Talcum Powder Lawyers For Ovarian Cancer Lawsuits

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Did You Use Talc Baby Powder?

Have You Been Diagnosed With Ovarian Cancer?

Talcum powder lawyers are filing Talcum Powder lawsuits for women who have gotten ovarian cancer from Talcum Powder.

Think talcum powder and many of us picture chortling babies and smiling mothers changing diapers. Nothing seems more safe and wholesome. And many women use talc products daily, as well, for feminine hygiene and after showering.

Do you remember this famous phrase from Johnson & Johnson s Shower to Shower  ads?  Just a sprinkle a day helps keep odor away. Well that sprinkle is now resulting in  women  filing  lawsuits against Johnson & Johnson claiming  that talc in this and other products led to them developing  ovarian cancer. They claim that the they  should have been warned.

Johnson s baby powder was one of the company s household name  products.  It has been sold for more than a 100 years. Now they say it can cause ovarian cancer?  A recent lawsuit awarded $72 million to a woman whose ovarian cancer could be scientifically linked to use of Talc.

But, you say,  I have been using this product for years. Since I was a  teenager or younger and they knew and did not tell us? Yes, in the  last few decades, studies have suggested a possible link between talc and ovarian cancer.

These studies go back, he says, to a British study in 1971. Researchers reported that microscopic analysis of 13 ovarian tumors found talc particles in 10 of them. Several other studies followed in the early 1980s in the United States and Europe and suggested that women who use talc feminine hygiene products may have up to a 35% higher risk of ovarian cancer than women who don’t those products.

The Johnson and Johnson website proclaims  Few ingredients have demonstrated the same performance, mildness and safety profile as cosmetic talc, which has been used for over 100 years by millions of people around the world. It goes on to note that talc is used in a range of other consumer products such as toothpaste, chewing gum, and aspirin.

If you think you have gotten ovarian cancer from Talcum powder contact us today to speak to a Talcum Powder lawyer

Bard IVC Filters Get National Attention | IVC Lawyers Filing Lawsuits

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Bard IVC Lawsuits Are Being Filed By IVC Filter Lawyers

Bard IVC Filter Injury Lawsuit News

The Bard IVC filter lawsuits came to national awareness with the NBC Nightly News segment on IVC filter complications.

A National broadcast has raised public awareness of current lawsuits filed by IVC filter lawyers against Bard. Lawsuits have been filed for patients whi have had a Bard IVC filter break or fail. These IVC lawsuits are consolidated as multidistrict litigation, MDL 2641 Bard IVC Filters Products Liability Litigation.

The Bard IVC lawyers of our Bard Injury Lawyer Network are pleased to see that there is now an awareness as these filters are primarily implanted in an older population. Attorneys representing families in IVC filter lawsuits are now accepting lawsuits for inclusion in the Bard IVC Filter MDL.

The Bard IVC filters are breaking, fracturing, and moving inside the body, causing damage to the heart and lungs and resulting in stroke and death according to adverse incident reports.

Our National Bard IVC Filter Helpline is ready to assist families, victims and caregivers. The National Bard IVC filter lawyers are accepting claims from victims, and their family members for injuries and deaths from the Bard IVC filter.

The vena cava filters are implanted in the veins of patients to catch blood clots before they reach the lungs. The filters have complications including vein and organ perforation, migration and breakage. This can result in injury or even death of patients.


Xarelto Extensive Bleeding Lawsuits Increase

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Xarelto is a medication which thins the blood. Xarelto has been shown to cause excessive bleeding resulting in serious injury and sometimes death. There is no way to stop the bleeding. Xarelto lawyers are filing lawsuits against the manufacturer for lack of warnings regarding their medication.

In December 2014, the U.S. Judicial Panel on Multidistrict Litigation (JPML) centralized all federal Xarelto lawsuits into one court in the Eastern District of Louisiana. At the time, about 50 product liability lawsuits were pending in the court. That number has now increased to about 400.

Not long after the Xarelto MDL was established, Philadelphia consolidated all state Xarelto lawsuits into a mass tort in the Philadelphia County Court of Common Pleas. What started as about 70 cases has now increased to about 200.

Defendants Resisted Formation of Mass Tort

Plaintiffs involved in Xarelto lawsuits claim that Johnson & Johnson subsidiary Janssen Pharmaceuticals and Bayer Healthcare Pharmaceuticals—manufacturers of the drug—should be held liable for damages associated with serious Xarelto side effects, including severe gastrointestinal bleeding and sometimes death.

The defendants initially resisted consolidating cases in Philadelphia, arguing that New Jersey would be a better location, since that’s where the company headquarters are located. They added that most plaintiffs also lived in other states, so it didn’t make sense to bring all cases to Pennsylvania.

The cases all do not involve common issues of fact, either, the defendants argued, since Xarelto is approved for multiple purposes. These include the prevention of blood clots after hip and knee replacement surgery, and the reduction of stroke risk in patients with non-valvular atrial fibrillation.

The court disagreed, stating the cases did share common issues of fact, that the defendants had strong ties to Pennsylvania, and that the Philadelphia court was an appropriate forum for the mass tort.

The companies expressed their intentions to defend against the claims brought in litigation, maintaining that Xarelto has a favorable benefit-risk profile.

Drug Makers Failed to Warn About Serious Xarelto Side Effects

The FDA approved Xarelto in 2011. Manufacturers immediately marketed it as a more convenient option to warfarin, the leading anti-coagulant for decades, because it came in a once-daily dose and required no dietary restrictions.

Within just a year, however, reports of excessive bleeding began coming in, numbering more than 1,000 by June 30, 2012—at least 65 of those involving the death of the patient. By the end of that year, more than 151 people had died in events related to Xarelto.

Plaintiffs filed lawsuits to recover damages, claiming that the drug makers had failed to provide proper warnings on the labels. Patients were left in the dark, for instance, on the fact that there was no readily available antidote to Xarelto bleeding. While all blood thinners carry some risk of bleeding, patients taking warfarin can have that bleeding stopped with vitamin K injections. There is no such solution for patients on Xarelto, making bleeding events much more serious and potentially deadly.

State and Federal Courts to Coordinate Pre-Trial Proceedings

Both parties plan to coordinate the mass tort with the Xarelto MDL. In a recent case management conference, for instance, held in April 2015, the MDL court noted that five days before each future status conference, the defendants are to identify and share any Xarelto lawsuits pending in state courts, to facilitate coordination.

If you or a loved one has been injured by Xarelto contact us for an Xarelto attorney.

GranuFlo Recall, Dialysis Medication Lawsuits, Heart Attack From Dialysis Medication Lawyers

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GranuFlo is used in Dialysis treatment. it has been recalled due to sudden heart attacks and deaths. Heart attack from dialysis medication lawyers are filing lawsuits for deaths from dialysis medications.

Definitions and Kindney Disease Overview

Chronic kidney disease (CKD): any condition that causes reduced kidney function over a period of time. CKD is present when a patient’s glomerular filtration rate remains below 60 milliliters per minute for more than 3 months or when a patient’s urine albumin-to-creatinine ratio is over 30 milligrams (mg) of albumin for each gram (g) of creatinine (30 mg/g).

End-stage renal disease (ESRD): total and permanent kidney failure. When the kidneys fail, the body retains fl uid. Harmful wastes build up. A person with ESRD needs treatment to replace the work of the failed kidneys.

Acute kidney injury (AKI): sudden, temporary, and sometimes fatal loss of kidney function

incidence: the number of new cases of a disease in a given time period

prevalence: the number of existing cases of a disease at a given point in time


Chronic Kidney Disease, Dialysis and GranuFlo. GranuFlo is a Threat to Seniors

  • The incidence of CKD is increasing most rapidly in people ages 65 and older.
  • The incidence of recognized CKD in people ages 65 and older more than doubled between 2000 and 2008.
  • The incidence of recognized CKD among 20- to 64-year-olds is less than 0.5 percent.

CKD Prevalence , GranuFlo Threat in 60 and Over Population

The prevalence of CKD is growing most rapidly in people ages 60 and older.
Between the 1988–1994 National Health and Nutrition Examination Survey (NHANES) study and the 2003–2006 NHANES study, the prevalence of CKD in people ages 60 and older jumped from 18.8 to 24.5 percent.
During that same period, the prevalence of CKD in people between the ages of 20 and 39 stayed consistently below 0.5 percent.

Dialysis Statistics By State

  • Alabama: 7,334
  • Alaska: 350
  • Arizona: 6,747
  • Arkansas:2,905
  • California: 45,047
  • Colorado: 3,360
  • Connecticut: 3,497
  • DC:1,809
  • Delaware: 1,170
  • Florida: 20,365
  • Georgia: 14,086
  • Hawaii: 2,449
  • Idaho: 916
  • I llinois: 15,268
  • Indiana: 6,539
  • Iowa: 2,296
  • Kansas: 2,384
  • Kentucky: 4,262
  • Louisiana: 7,287
  • Maine: 975
  • Maryland: 7,823
  • Massachusetts: 5,123
  • Michigan:12,293
  • Minnesota: 3,697
  • Mississippi:5,456
  • Missouri:6,467
  • Montana: 627
  • Nebraska:1,473
  • Nevada: 2,294
  • New Hampshire: 690
  • New Jersey: 10,580
  • New Mexico: 2,451
  • New York: 23,612
  • North Carolina: 12,895
  • North Dakota: 501
  • Ohio: 13,761
  • Oklahoma:3,793
  • Oregon: 2,703
  • Pennsylvania: 14,201
  • Puerto Rico:4,032
  • Rhode Island: 838
  • South Carolina: 7,199
  • South Dakota: 689
  • Tennessee: 7,482
  • Texas: 32,383
  • Utah: 1,303
  • Vermont: 380
  • Virginia: 9,332
  • Washington: 5,026
  • West Virginia: 1,794
  • Wisconsin: 4,899
  • Wyoming:248


The high incidence of Dialysis treatment in Florida is due to the numbers of aging population. Our Florida Seniors are at risk for sudden heart attack form the dialysis medication GranuFlo and Naturalyte.

Fresenius labs has used GranuFlo and Naturalyte in Dialysis Treatments. Fresnius knew of the dangers and still used the medication. As a result many of our seniors have suffered cardiac arrest and heart problems

Fresenius Claima To Be Patient-Centered Care for Chronic Kidney Disease

Fresenius Medical Care North America is a major provider of kidney dialysis services and renal care products. We provide products, dialysis care services, education and support for Chronic Kidney Disease (CKD), including treatment options for later stage CKD.

Our dialysis care services include hemodialysis, peritoneal dialysis, education tools and transplant support services, in-center, at home, or in a hospital, to fit our patients needs. We manufacture and distribute a variety of dialysis products and equipment, including dialysis machines, dialyzers and other dialysis-related supplies.

FDA Issues Class 1 Recall of GranuFlo

In late March of 2012, the FDA became aware of the apparent link between GranuFlo and cardiac arrest, according to the New York Times. In response to information about this threat to dialysis patients, which GranuFlo producer Fresenius had not made public, the FDA issued a Safety Communication warning about the dangers of alkali dosing errors for products like GranuFlo and NaturaLyte in hemodialysis patients.

In June, the FDA then issued a Class 1 recall of GranuFlo. This is the most serious class of recall, issued when the FDA deems there to be "a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death." The FDA described the reason for the recall thus:

The manufacturer is cautioning clinicians to be aware of the concentration of acetate or sodium diacetate (acetic acid plus acetate) contained in Fresenius Naturalyte Liquid and Granuflo Dry Acid Concentrate. Inappropriate prescription of these products can lead to a high serum bicarbonate level in patients undergoing hemodialysis. This may contribute to metabolic alkalosis, which is a significant risk factor associated with low blood pressure, hypokalemia, hypoxemia, hypercapnia and cardiac arrhythmia, which, if not appropriately treated, may culminate in cardiopulmonary arrest. This product may cause serious adverse health consequences, including death.

GranuFlo Lawsuits Mounting Up. Protect Our Seniors, File Your GranuFlo Lawsuit Today

GranuFlo and NaturaLyte lawsuits are being filed in courts around the country, after hundreds of patients suffered cardiac arrest, sudden cardiac death. Pur seniors are in danger. Serious heart problems have been reported following the use of the drugs during dialysis treatments. While Fresenius Medical, the manufacturer of GranuFlo and NaturaLyte, learned of the risks associated with the dialysis drugs in 2011, a GranuFlo and NaturaLyte recall was not announced until months later. GranuFlo and NaturaLyte lawsuits are now being filed on behalf of our seniors who are victims of serious heart side effects within 48 hours of a dialysis treatment with GranuFlo and Naturalyte. Problems include: sudden cardiac death, cardiopulmonary arrest, heart attack and the development of heart problems.

File Your GranuFlo Lawsuit and Protect Your Loved Ones. Get Justice form Manufacturers who value profits over harm to people. If you, a loved one or someone you are a caregiver for has been injured by a dialysis medication call the GranuFlo Lawyer Helpline of Free Legal Shiels today.