Fort Worth

Mirena IUD Lawyers Accepting Mirena IUD Lawsuits Nationwide

Free Legal Shield Mirena IUD Lawyers are accepting Mirena IUD cases where the device has migrated from position to the uterus, abdomen or a nearby organ. The device becomes embedded and causes a perforation and usually needs to be surgically removed.

Can you answer yes to any of these questions? If so, we need to hear from you today.

Were there any complications with the original insertion?
Do you have a perforation?
Has the device been surgically removed?

Symptoms to watch out for include:

Lower abdominal pain
Heavy vaginal bleeding
Inability to locate the Mirena IUD string
Bloating,and pain in the abdomen
Nausea, Vomiting, Chills, Fever and Rapid heartbeat

Serious side effects that have been linked to Mirena include:

  • Embedment in the uterus
  • Embedment in the abdomen or a nearby organ
  • Erosion of adjacent areas such as the vagina
  • Intestinal perforations or obstruction
  • Perforation of the uterus

Mirena IUD Lawsuits Alert

Mirena IUD lawyers are filing Mirena lawsuits for a implanted Mirena IUD needing to be surgically removed because it migrated from its original position and perforated the uterine lining, You may have a potential Mirena lawsuit.

Legal Shield has launched an aggressive outreach campaign to locate all women who have had a perforation of the uterus or abdomen or another organ.

Lawyers for Airplane Accidents and Aviation Crash Injuries

Nationwide Airplane Crash Lawyers

Nationwide Lawyers for Airplane Accidents and Aviation Crash Injuries

An airplane disaster with loss of life can be devastating to a family and can cause severe emotional distress. If you or a loved one is a victim of an aircraft accident, control tower misconduct, or pilot negligence, not only do you need an aggressive airplane accident lawyer, but you also need emotional support. An airplane disaster can affect you for months, and live in your memory for years. Our experienced airplane crash lawyers provide effective representation while understanding your emotional needs after such a traumatic experience.

When an airplane crash occurs, people try to make sense of what happened in order to deal with the anxiety and stress of the situation. Emotional and psychological trauma results from the extraordinarily stressful event. This may shatter your sense of security, making you feel helpless and vulnerable in a dangerous world. The emotional damage can linger long after the crisis is over and a permanent mark may be left on your psyche. Further, airplane accident lawsuits do not settle quickly or easily thus, adding to your overall stress. For this reason, your choice of an airplane accident law firm is extremely important. A law firm inexperienced with these disasters may not understand the extent of your emotional trauma. The aircraft disaster team at Injury Lawyers USA has over 15 years of experience, as they have served the needs of airplane crash victims since 1996.

After a disaster of this magnitude, you may begin to have some common psychological reactions such as:

– Disbelief, shock, and post traumatic stress
– Fear and anxiety about the present and the future
– Disorientation; difficulty making decisions or concentrating
– Apathy and emotional numbing
– Nightmares and reoccurring thoughts about the event
– Irritability, anger, and occasional outbursts
– Sadness and depression
– Feeling powerless
– Changes in eating patterns; loss of appetite or overeating
– Crying for “no apparent reason”
– Headaches, back pains, and stomach problems
– Difficulty sleeping or falling asleep; sleep deprivation symptoms
– Increased use of alcohol and drugs

Facts About Airplane Accident Law

Airplanes are considered common carriers. This means that aircraft employees are required to use the highest degree of care in transporting you to your destination. The airplane carrier is also required to inspect and maintain all equipment, and workers are required to have the skill to carry out their duties in order to protect your safety. When the airline fails to uphold these safety standards, accidents can occur. The airplane accident lawyers at Injury Lawyers USA will argue that the airline failed to satisfy its duty of the highest care to you.


If you or a loved one has been injured in an airplane accident, seek out a law office that will aggressively pursue your case while providing you with the care and concern you deserve. As it may be difficult to make decisions during a time of such vulnerability, it is necessary to trust the airplane crash lawyer you retain. Injury Lawyers USA is here for you. Our lawyers are experienced in dealing with such issues are available to guide you and help you during this difficult time.

Airplane crashes and injuries can be caused by:

-Dangerous conditions inside the aircraft
-Careless handling of the aircraft
-Severe turbulence
-Negligent actions by incompetent flight staff
-Faulty maintenance of the aircraft and equipment
-Poor flight and airport traffic control
-Faulty equipment at the airport

Many federal, state, and international laws regulate standards for the maintenance, operation, and safety of airplanes. However, even though these laws help protect passengers of airlines, an accident may still happen. Aviation law covers personal injuries that occur aboard aircraft, including slip and fall accidents and wrongful deaths that may occur in the rare case that an airplane crashes. The laws are highly specialized, and the causes of airplane accidents may be difficult to determine. Our lawyers are skilled litigators assisting crash victims and families nationwide and internationally. If you or a loved one has been injured in an airplane accident, your lawyer can review your case, protect your rights, and help you get the compensation you deserve. Our airplane accident lawyers at Injury Lawyers USA are supportive of your personal and emotional needs and fierce in their legal representation.

Contact us if you or a loved one has been a victim of:

U.S. airline accident l awyer ,
Private aircraft accident lawyer,
International aviation accident lawyer,
Helicopter crash lawyer,
Sightseeing air tour accident,
Charter aircraft accident,
Medical aircraft crash,
Flight school accident,
Seaplane crash,
Air Balloon crash,

Fighting for the people…….Demanding truth, justice and accountability Airplane Crash Wrongful Death

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

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.


Dialysis Injury Help Center, GranuFlo Naturalyte Helpline

Lawyers for GranuFlo and Naturalyte are filing lawsuits for dialysis injury from Granuflo and Naturalyte. Fresenius Medical Care’s dialysis product GranuFlo is a medication that dialysis centers use to treat acute and chronic kidney failure.

Your kidneys clean the blood of waste products and help maintain the body’s pH level. When they fail, the body’s pH level become more acidic than is should be. Kidney failure is treated with chemicals that help the body convert ph level. These substances convert into the alkaline substance bicarbonate, which neutralizes some of the acid buildup in the blood stream.
GranuFlo and Naturalyte have had issues with this conversion and have shown instances of immediate heart attacks as a side effect. GranuFlo contains more bicarbonate than other dialysates.

The June 2012 New York Times article describes Fresenius’s knowledge of these risks of granuFlo and Naturalyte and the product’s high bicarbonate level. According to the article, Fresenius sent a memo to its clinics warning that the higher bicarbonate levels in GranuFlo had caused 941 heart attacks in the company’s own clinics in 2010, leading the company’s researchers to estimate that GranuFlo increases a patient’s risk of heart attack by six times. Fresenius did not send the memo to GranuFlo-using clinics that the company didn’t own, however, until March 29, 2012, when the FDA consequently began investigating Fresenius for possible violations of federal regulations, the Times reports.

Currently GranuFlo and Naturalyte lawyers are accepting claims against Fresenius for immediate hear attack form their GranuFlo and Naturalyte products. A number of dialysis patients may have already been injured by GranuFlo. If GranuFlo diaysis medication caused a sudden heart attack or cardiac arrest, hemodialysis cardiac arrest or cardiopulmonary arrest, stroke, or arrhythmia speak to a GranuFlo lawyer now by calling the GranuFlo legal team of free legal Shield. We seek justice for seniors.

Mesothelioma Lawsuits, Mesothelioma Lawyers, Asbestos, Lung Cancer

Mesothelioma is a fatal lung cancer caused by exposure to asbestos. Certain work environments are more prone to causing mesothelioma.

  • Shipyard Workers
  • Construction Workers
  • Power Plant Workers
  • Chemical Plant Workers
  • Industrial Workers
  • Insulators
  • Boiler Workers
  • Auto Mechanics

Types of mesothelioma

  • Pleural mesotheliomas start in the chest.
  • Peritoneal mesotheliomas begin in the abdomen.

Symptoms of Mesothelioma

  • Shortness of breath and
  • A heavy feeling in the chest area.
  • Pain under the rib cage.
  • Pain or swelling in the abdomen.
  • Lumps in the abdomen.
  • Weight loss for no known reason.

Mesothelioma Comes from Inhaling Asbestos For Long Periods Of Time

When a person breathes in the small asbestos fibers, they remain in the lungs and cause scar tissue to form on the the tiny air sacs where oxygen and carbon dioxide are exchanged. The amount of oxygen that is available to the body is reduced through asbestos exposure and worsened through repeated inhalations for long periods of time.

Notable asbestos verdicts in the United States include:
Mississippi

In May 2011, the current largest plaintiff s asbestos verdict was awarded to a former oil refinery worker. Union Carbine and Chevron Phillips Chemical were instructed to pay the man $322 million.
San Francisco, California

Alfred Todak, a former Navy electrician, was awarded $22.7 million, and his was wife was awarded $11 for loss of consortium.
Madison County, Illinois

Madison County s asbestos verdicts have typically favored the plaintiff, including the 2000 Hutchinson v. Shell Oil Company case in which a man was awarded a total of $34.1 million.

Incidence of Mesothelioma

State/Region Incidence per 100,000
New Jersey 1.52
Seattle-Puget Sound 1.44
Louisiana 1.37
Connecticut 1.08
Greater California 1.06
Utah 1.02
New Mexico 0.99
Detroit 0.89
Kentucky 0.85
Iowa 0.80
Georgia 0.70

The six states with the highest mesothelioma death rates include: Maine, Wyoming, West Virginia, Pennsylvania, New Jersey and Washington

Mesothelioma Lawyers

If you or a loved one has been diagnosed with mesothelioma or asbestos related cancer call our mesothelioma helpline today. We will connect you with an experienced mesothelioma, mass tort lawyer. Mesothelioma lawsuits are mass torts and must be handled by an experienced mass tort lawyer.

Januvia, Byetta Risks of Pancreatic Cancer, Lawyers Looking At Lawsuits

New Information on Byetta and Januvia is gaining interest by lawyers for Pancreatic and Thyroid Cancer. Type II Diabetics are potential victims of cancer from these Diabetic drugs.

Popular diabetes drugs may raise pancreatic cancer risk, study suggests
By Steven Reinberg, HealthDay
Updated 9/23/2011 6:15 PM

People with type 2 diabetes taking the drugs Januvia or Byetta might have an increased risk of developing pancreatitis and pancreatic cancer, a preliminary study suggests.
Sponsored Links

The study also found that Byetta (exenatide) may raise the risk of thyroid cancer.

Although the links aren t conclusive, they merit further investigation, the researchers noted.

"We have raised concern that there may be a link, but we haven t confirmed it," said lead researcher Dr. Peter Butler, director of the Larry L. Hillblom Islet Research Center at the University of California, Los Angeles. "We need to do more work to figure out whether this is real or not."

Both drugs help control blood sugar levels by encouraging production of a hormone called glucagon-like peptide 1 (GLP-1).

Januvia (sitagliptin) and Byetta, an injectable drug, are a new way of treating type 2 diabetes, and they potentially have advantages over older medications, Butler said. But, because these drugs are new, they re "the ones we know least about," he said. "When new drugs come out, the long-term side effects of these drugs are not well understood."

For the study, recently published in the journal Gastroenterology, Butler s team used 2004-2009 information in the U.S. Food and Drug Administration s database on adverse events, which are reported by doctors whose patients use these drugs.

When compared to other treatments, the researchers found a sixfold increase of reported cases of pancreatitis (inflammation of the pancreas) linked to patients taking Januvia or Byetta; a 2.9-fold increase in reported cases of pancreatic cancer among those taking Byetta and a 2.7-fold increase of reported pancreatic cancers among Januvia users.

In addition, they also noted an increase in reported cases of thyroid cancer with Byetta.

This latest study builds on earlier research, published in a 2009 issue of Diabetes, which found an increase in pancreatitis in rats whose GLP-1 levels were raised, the researchers said.

Butler is quick to point out that these increases in pancreatic cancer risk, while statistically significant, are not specifically related to patients, but rather to an increase in doctors reporting these cases to the FDA.

"It is important to avoid alarmism and have people stop medicines that they may be benefitting from when the risk is not yet defined," he stressed.

"If the drug and you are working well together, I wouldn t say there is any reason to stop the drug, based on the evidence we have right now," he said. "But if you have any concern you should talk to your doctor about it."

Being overweight is an important risk for both pancreatic cancer and type 2 diabetes, Butler noted. So the first advice to overweight patients with type 2 diabetes is to lose weight. "By doing that, you reduce the risk of pancreatic cancer," he said.

In addition, the first medication used to control blood sugar in type 2 diabetics is metformin, which by itself may reduce the risk for pancreatic cancer, Butler said. Metformin is an older drug with a well-known safety profile, he noted.

Dr. Mary Ann Banerji, director of the Diabetes Treatment Center at SUNY Health Science Center Brooklyn in New York City, said that "this is not perfect data."

However, Banerji does not prescribe these drugs for patients who have had a history of pancreatitis or a family history of thyroid cancer. There are alternatives such as metformin and insulin, as well as Avandia and Actos, she said, but studies have turned up an increased risk for heart attack and heart failure in the last two drugs. The FDA has removed Avandia from pharmacy shelves, and the agency issued a warning last summer that there is a possible increased risk of bladder cancer in patients who take Actos for more than a year.

The concerns about Januvia and Byetta "should not be blown out of proportion," Banerji said. "You prescribe them on an individual basis, because, in the end, all of medicine is individual," she said. "We should use these drugs judiciously along with metformin."

Industry representatives, insisting that no studies involving these drugs have found an increased risk of pancreatitis or pancreatic cancer, stand by their products. The database used for the study contains information on doctor-reported cases and does not reflect cause-and-effect, they said.

Dr. Barry Goldstein, vice president and therapeutic area head for diabetes and endocrinology at Merck Research Laboratories, which makes Januvia, said that "there has been no association shown between Januvia and pancreatitis."

"We have full confidence in Januvia, which is used by millions of patients around the world," he said.

Anne Erickson, a spokeswoman for Amylin Pharmaceuticals, makers of Byetta, said that "the conclusions of the study are in contrast to other nonclinical, clinical and adequately conducted post-marketing epidemiological studies."

Epidemiological studies have not established a significantly increased risk of pancreatitis associated with Byetta, she said. "To date, the available data do not demonstrate that exenatide increases the overall risk of cancer in humans."

Another expert, Dr. Ronald Goldberg, professor of medicine, biochemistry and molecular biology at the University of Miami Miller School of Medicine, said the findings merit consideration. "I don t think the study is definitive, but it raises a flag and is clearly something we need to pay attention to going forward."

There is "more benefit than risk with these drugs, based on our current knowledge," he

GranuFlo Lawyers, NaturaLyte Lawsuits

Fresenius Medical is the manufacturer of GranuFlo and NaturaLyte acid concentrate. These are drugs used in dialysis treatment. There has been a recall of these dialysis drugs and lawsuits are being filed.

Injury and death has resulted from these drugs:

  • GranuFlo cardiovascular death,
  • GranuFlo sudden cardiac death,
  • GranuFlo cardiopulmonary arrest,
  • GranuFlo heart attack,
  • GranuFlo catastrophic cardiovascular injuries

Fresenius manufactures GranuFlo and NaturaLyte used in dialysis. These drugs cause alkalosis, a condition associated with an increase in cardiovascular fatalities.

The FDA received complaints describing alkali dosing errors that occurred during hemodialysis using dialysate concentrates containing acetic acid and acetate. When metabolized, these potential sources of alkali can contribute to elevated bicarbonate levels in patients undergoing hemodialysis.

This can contribute to metabolic alkalosis, which is a significant risk factor associated with :

Low blood pressure

Cardiopulmonary arrest

Cardiac arrhythmia

Sudden heart attack

Stroke

Hemodialysis cardiopulmonary arrest

A study which was conducted between January and December of 2010 found that patients with pre-dialysis bicarbonate levels greater than 28mEq/L were 4.7 times more likely to suffer a cardiac arrest. The study also discovered that patients with pre-dialysis potassium lower than 4 mEq/L had a 6.3 times higher risk of cardiac arrest.

In May 2012 the FDA notified health care providers to consider the presence and quantity of acetate, citrate, and/or acetic acid in dialysate concentrates when determining the patients’ dialysate prescription.

There is a GranuFlo and NaturaLyte Class 1 Recall

Serial numbers for recalled Naturalyte Liquid Acid Concentrate range from:

08-0231-4, 08-1001-0, 08-1201-8, 08-1231-3, 08-1251-1, 08-1301-4, 08-2201-5, 08-2231-2, 08-2251-0, 08-2301-3,08-2351-8, 08-3201-4, 08-3231-1, 08-3251-9, 08-3301-2, 08-4123-1, 08-4223-7, 08-4225-1, 08-4230- 2, 08-4231-0, 08-4323-5, 08-4325-1, 13-1251-1, 13-2201-5, 13-2231-2, 13-2251-0, 13-3231-1, 13-3251-9, 13-4123-1, 13-4220-1, 13-4225-1, 13-4325-

Serial numbers for recalled Naturalyte GranuFlo (powder) Acid Concentrate range from:

OFD1201-3B, OFD1251-3B, OFD2123-3B, OFD2201-38, OFD2220-3B, OFD2223-3B, OFD2225-3B, OFD2231-3 B, OFD2251-3B, OFD2301-3B, OFD2323-3 B, OFD2325-3B, OFD3201-3B, OFD3231-3B, OFD3251-3B, OFD3301-3B

GranuFlo & NaturaLyte is one of the most widely prescribed dry acid products used for dialysis at Fresenius clinics, as well as other hemodialysis centers that purchase their dialysis supplies from Fresenius. It is estimated that 125,000 patients in non-Fresenius clinics are treated with GranuFlo.

Dilaysis Patient Alert

If you, a loved one or someone you care for has been injured by these products contact us for a GranuFlo and NaturaLyte lawsuit.

Vaginal Mesh Update, Vaginal Mesh Lawyers

Vaginal mesh lawsuits have been consolidated in three major jurisdictions: West Virginia, New Jersey and Georgia. There are a total of 6 MDL s that are currently active. No matter where your case is filed it will most likely end up in one of these under the auspices of a lead cousel that will proceed on your behalf. These are not class actions but, consolidations. This is very different as it is still on an individual settlemement basis. Just to give you a point of reference the first Yaz settlements have settled for $250,000 for the first grouo of victims and the DePuy for $600,000 for six victims.

Problems with vaginal mesh systems marketed by a number of different medical device manufacturers have caused thousands of women throughout the United States to suffer severe injuries. The major manufactures involved in the litgations are Johnson and Johnson, Bard, Boston Scientific, and American Medical. Johnson and Johnson has just recently pulled 4 of the Gynecare mesh off the market and has published a new label change for one still on the market.

The vaginal mesh lawsuit lawyers are filing mesh lawsuits for women who have received any type of surgical mesh or bladder sling to repair pelvic organ prolapse, which could include:

Bard Avaulta Support System
AMS Elevate Prolapse Repair System
AMS Apogee Vault Suspension System
AMS Perigee System
AMS Monarc Sling System
AMS Sparc Sling System
Ethicon Gynecare Gynemesh
Ethicon Gynecare Prolene Soft Mesh
Ethicon Gynecare Prolift Pelvic Floor Repair System
Ethicon Gynecare TVT Transvaginal Sling
Boston Scientific Pinnacle Pelvic Floor Repair Kit
Boston Scientific Uphold Vaginal Support System
UGYTEX Dual Knit Mesh
Coviden IVS Tunneler Sling

Due to the risk of vaginal mesh complications, the FDA warned in July 2011 that doctors should recognize that in most cases, pelvic organ prolapse can be treated successfully without a bladder sling or pelvic mesh. Thousands of women had a bladder sling or vaginal mesh implanted in recent years, and compensation may be available for serious injuries caused by the defective and dangerous design of the pelvic support systems.

Mesh lawsuits should be filed quickly as the staute of limitations is running close in many states and some are past the filing date already.

Bladder Sling Lawyers, Vaginal Mesh Lawsuits

The bladder mesh is a vaginal mesh product primarily used for urinary incontinence. This mesh sling has caused severe complications and bladder mesh lawyers are filing lawsuits. Many women with a bladder mesh do not realize they are eligible to file a vaginal mesh lawsuit.

What is a Bladder Sling?

Urethral sling or bladder sling is used to treat urinary incontinence by placing a sling around the urethra to lift it back into a normal position and to exert pressure on the urethra to aid urine retention. The sling is attached to the abdominal wall. A bladder sling is a mesh device and is part of the vaginal mesh litigation. The complications of a failed bladder sling is increased incontinence or trouble voiding. Many women have needed to self catherize.

Bladder Sling Complications?

According to the July 2011 FDA news release, the most common complications associated with surgical mesh bladder slings is erosion thru the vaginal wall or into the bladder, pain during sexual intercourse, bleeding, infection, perforation of various pelvic organs (bladder, colon, vaginal walls), and urinary incontinence or problems voiding as well as; neuromuscular problems, emotional problems, mesh contraction/shrinkage, and even a reoccurrence of POP and/or SUI.

Bladder sling lawsuits are being filed on a contingency fee basis against the mnaufacturers of the bladder sling:

Bard Avaulta Support System
AMS Elevate Prolapse Repair System
AMS Apogee Vault Suspension System
AMS Perigee System
AMS Monarc Sling System
AMS Sparc Sling System
Ethicon Gynecare Gynemesh
Ethicon Gynecare Prolene Soft Mesh
Ethicon Gynecare Prolift Pelvic Floor Repair System
Ethicon Gynecare TVT Transvaginal Sling
Boston Scientific Pinnacle Pelvic Floor Repair Kit
Boston Scientific Uphold Vaginal Support System
UGYTEX Dual Knit Mesh
Coviden IVS Tunneler Sling

Contact us today.

Stryker Hip Replacement Lawyers, Stryker Hip Replacement Helpline

Adding to the Zimmer and DePuy metal on metal hip replacement Stryker has recalled it s latest metal component hip replacement implant. Stryker has voluntarily recalled the Rejuvenate metal component hip replacement implant and ABG II modular- neck stems
Stryker has voluntarily stopped market distribution of these hip replacements due to increased risk of injury. The hip replacement implants have been shown to fret or corrode, harming body tissue and causing pain and swelling. Other injuries include:

  • Severe inflammatory reactions
  • Pain in the groin
  • metal toxicity ort poisoning
  • high metal levels in the blood
  • need for additional surgery
  • Breakdown of muscles, tendons and other soft tissues in and around the hip joint
  • Loss of surrounding bone
  • Loss of mobility

While other types of hip implants such as those made by Johnson & Johnson and DePuy Orthopaedics Inc. involve a metal ball rubbing against a metal socket, the Stryker Rejuvenate products involve a metal neck inside a metal stem. The Stryker Hip replacement Helpline and hip replacement lawyers are reaching out to all victims of the failed device for a potential multi district litigation.

The products have metal components and although they are not metal on metal run the same risks of chromium and cobalt toxicity poisoning. If you have been injured you are advised to contact your doctor immediately and contact the Stryker Hip Replacement Helpline for a Stryker lawyer