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Lawyers for Airplane Accidents and Aviation Crash Injuries

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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 news Updates, Dialysis Medication Lawsuits Consolidation

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GranuFlo and Naturalyte heart attack form dialysis medication lawyers are filing lawsuits for cardiac injury and death from GranuFlo and Naturalyte.

There was a class 1 recall of GranuFlo last year due to cardiac injury during or just after dialysis treatment. NaturaLyte is a liquid acid concentrate and GranuFlo is a dry acid concentrate. Both products contain sodium acetate that converts to bicarbonate at higher then expected rates leading to immediate cardiac arrest in many dialysis patients and cardiac injury bin others.
At year s end in 2012,a Motion to Consolidate the cases into multidistrict litigation (MDL) for all federal lawsuit was filed. A request has been filed with the U.S. Judicial Panel on Multidistrict Litigation asking that all Naturalyte and GranuFlo lawsuits filed in U.S. District Courts throughout the country be consolidated for pretrial proceedings in the District of Massachusetts.
Early in 2013, Fresenius said in court papers that it agreed that consolidation of the NaturaLyte and Granuflo litigation was appropriate and supported the transfer of the cases to the District of Massachusetts
On January 3, several Plaintiffs with pending lawsuits have objected to centralizing the cases in Massachusetts, indicating that the litigation should be consolidated in the southeast, because of the number of cases filed in that region. Their choices are the Southern District of Mississippi and the Northern District of Alabama have been requested. Many Florida retired seniors are dialysis patents and have been injured or killed sue to a cardiac episode from GranuFlo or Naturalyte.

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

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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

Fosamax Lawyers for Women Injured By Fosamax, Femur Fractures

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Fosamax Femur Fracture Lawyers

Our Fosmax lawyers are filing lawsuits for Femur faracture from Fosmax.

Fosamax (alendronate) is a part of the class of bisphosphonates. Fosamax alters the cycle of bone formation and breakdown in the body. Fosamax slows bone loss while increasing bone mass, which may prevent bone fractures.

Fosamax is used in men and women to treat or prevent osteoporosis that is caused by menopause or by taking steroids. Fosamax is also used to increase bone mass in men who have osteoporosis, and to treat Paget s disease of the bone in men and women.

However, Fosamax has been a central focus of lawsuits. Fosamax has been linked to a number of severe side effects that has required many revisions of the Fosamax Warning label. These side effects have brought about a wide range of Fosamax lawsuits. Fosamax has been shown to cause Osteonecrosis of the Jaw Injury, Femur Fractures, and Severe Musculoskeletal Pain.

FDA Issues Fosamax Warning

On Oct. 13, 2010, the U.S. Food and Drug Administration issued a Fosamax safety about the risk of atypical femur fractures. The victims of Fosamax are mostly post menapausal women who lose bo have osteoporosis due to loss of estrogen. Fosamax has caused what it was prescibed to help, femur fractures.

Reports from the Hospital for Special Surgery and Columbia University Medical Center have reported that Fosamax changes bone remodeling in an unknown manner and may contribute to Fosamax Femur Fractures. Many medical journals have reported Femur faractures from Fosamax. According to the geriatric social worker who runs the helpline" Our concern is with the elderly who have been prescibed Fosamax. Femur fractures heal slower as we age and usually require long periods of rehabilitation and physical therapy."

The femur is one of the largest, and strongest bones in the body. The femur is the thigh bone. The femur extends from the hip joint down to the knee joint. Because the femur is such a strong bone, it can take tremendous force to cause a femur fracture. Spontaneous femur bone fractures are extremely unusual and serious for anyone but, especially serious for older women."

For the most part Femur fractures are caused by extremely high impact accidents like car accidents or Falls from a height although they can happen to the fragile elderly from a fall.

It is interesting to note that womwn may also have bone that is weakened by osteoporosis thae exact medical condition Fosamax was to help.

Femur fractures include:

  • Hip Fractures
  • Femoral Neck Fractures
  • Intertrochanteric Femur Fractures

Femur fractures almost always require surgery and long periods of rehabilitation and Physical therapy. Sometimes they result in a length variatopn due the a potential hip rotation during surgery and cam lead to poor balance. In some cases the pre- fracture level of functioning does not return completely.

Fosamax MDL Update

All Fosamax lawsuits alleging that the victim sustained an atypical femur fracture as a result of taking the bisphosphonate Fosamax, can also include victims who took similar medications such as Reclast or Boniva as long as they did, in fact, take Fosamax.

If you a family member or someone you are a caregiver for has a spontaneous femur fracture and is on one of these medications contact our Fosamax Helpline to find out if you can be included in the current Fosamax litigation underway.

Current Fosamax News

A U.S. District Court judge has ordered hundreds of Fosamax lawsuits returned to the state courts and out of the MDL.Judge John Keenan ordered that 200 Fosamax cases a month be returned to the state courts where they were filed.

GranuFlo Lawyers, NaturaLyte Lawsuits

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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.

Bladder Sling Lawyers, Vaginal Mesh Lawsuits

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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

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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

Pradaxa Breaking News, Pradaxa lawyers, Pradaxa Lawsuits, Pradaxa Bleeding

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Pradaxa has warnings for excessive bleeding. Pradaxa Helpline is concerned about Pradaxa and the elderly

The Pradaxa Helpline Has Pradaxa Lawyers to Help You

LONDON | Fri May 25, 2012 6:07am EDT

(Reuters) Doctors and patients should be given clearer guidance on how to avoid bleeding risks when using Boehringer Ingelheim s new stroke prevention pill Pradaxa, European regulators said on Friday.

The European Medicines Agency said data continued to confirm the positive benefit-risk balance of the anticoagulant medicine, despite cases of fatal bleeding, but advice on the risks should be strengthened.

Pradaxa is the first in a new class of medicines aimed at replacing the old and problematic drug warfarin. It is designed for use after hip and knee surgery and to prevent strokes in patients with atrial fibrillation, a form of irregular heartbeat common among the elderly.

Rival drugs include Xarelto, from Bayer and Johnson & Johnson, and Eliquis, from Bristol-Myers Squibb and Pfizer.

Pradaxa is an anticoagulant. Anticoagulants effect the clotting time of the blood. Pradaxa is described as a prescription blood-thinning medicine used to reduce the risk of stroke and blood clots in people with atrial fibrillation not caused by a heart valve problem. With atrial fibrillation, part of the heart does not beat the way it should. This can cause blood clots to form, increasing your risk of a stroke. Pradaxa lowers the chance of blood clots forming in your body. There is a chnce of excessive bleeding on Pradaxa that can be fatal.

We can locate a Pradaxa lawyer to help you:

Silicone Breast Implant Claims Lawyers, Silicone Breast Implant Class Action

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Breast implant Class Action lawyers Helping women with Dow Corning, Mentor and other Silicone breast implant claims.

Silicone breast implants caused silicone toxicity and Immune deficiency diseases with symptoms of:

  • Muscle Pain -Upper arms, neck, chest, upper back, thighs, buttocks
  • Joint Pain -hands, feet, toes, elbows
  • Pressure headaches
  • Ringing in ears
  • Sun sensitivity & rash; face, neck & upper chest
  • Hives
  • Intermittent tingling in legs, feet, arms, fingers, right upper back, neck and face
  • Many urinary tract and yeast infections
  • Burning lips, mouth, tongue
  • Dry eyes, nose, mouth, and vagina
  • Nausea, heartburn, constipation, diarrhea
  • Insomnia
  • Anxiety

And:

  • Breast Pain
  • Upper and Lower Back Pain
  • dry eyes
  • joint pain and swelling
  • myalgias
  • chronic fatigue
  • Lupus
  • numbness and tingling in extremities
  • photosensitivity
  • Chemical Sensitivities
  • Muscle Pain, Stiffness, Unusual Fatigue
  • Excessive Hair Loss
  • Achy or Swollen Joints
  • Extreme fatigue
  • Skin Rashes
  • Rheumatoid Arthritis
  • Polymyositis-Dermatomyositis
  • Mixed Connective Tissue Disease
  • Scleroderma
  • Sjogren s syndrome
  • Anemia
  • Sensitivity to Sunlight
  • Kidney Problems
  • Fever
  • Difficulty Swallowing or Breathing

Women are still suffering today and settlements are still pending for the Silicone Breast Implant Clas Action. If you currently are registered fo r one of the breast implant settlement manufacturers and need help with your claim call 1 877 522-2123

Women Filing nationwide Vaginal mesh lawsuits, vaginal Mesh lawyers

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The vaginal mesh has been wrecking havoc on womens lives and the numbers are just starting to reveal themselves. Wome have stories about their vaginal mesh and are ready to file vaginal mesh lawsuits. one of the women below:

Texarkana woman files personal injury lawsuit over vaginal mesh implant
5/21/2012 10:22 PM By Michelle Keahey, East Texas Bureau

TEXARKANA After suffering several complications allegedly stemming from transvaginal mesh implantation, a Texarkana woman has filed a personal injury lawsuit against the medical device manufacturer.

Peggy Green filed suit against Boston Scientific Corp., doing business as Mansfield Scientific Inc. & Microvasive Inc. on May 14 in the Eastern District of Texas, Texarkana Division.

Due to stress urinary incontinence, Green was surgically implanted with the Uphold Vaginal Support System, manufactured by the defendant, on May 14, 2010.

After her surgery, she began to experience complications such as vaginal pressure and pain, vaginal bleeding and/or dyspareunia. She states that these complications are the result of the implanted medical device.

The defendant is accused of breach of warranty, negligence, and failure to warn.

The plaintiff is seeking an award of compensatory damages, punitive damages, exemplary damages, incidental damages, consequential damages, attorney s fees, and court costs.

Green is represented by Erin K. Copeland of Fibich, Hampton, Leebron, Briggs & Josephson in Houston. A jury trial is requested.

U.S. District Judge Michael H. Schneider is assigned to the case.

This is just one of many vaginal mesh lawsuits. If you have been injured and your life destroyed by a defective vaginal mesh do not delay. There are statue of limitation issues. contact our vaginal mesh free legal department today.