Class Action Article

  • Physiomesh Hernia Mesh Lawyers: Physiomesh Hernia Mesh lawyers are filing Hernia Mesh lawsuits for your failed Physiomesh used to repair your hernia. Ethicon voluntarily withdrew the Physiomesh from the  market in May of 2016  after independent studies revealed high rates...

Class Action News

  • Stryker Femoral Heads Hip Replacement Lawyers: Stryker V40 Taper Hip Replacement Lawyers Stryker Hip Replacement Lawyers Hip Implant lawyers are filing hip replacement lawsuits for V40 Femoral head failure in the Stryker Hip Implant. In August 2016, Stryker contacted implanting physic...

Drug Class Actions

  • Taxotere Lawyers for Permanent Hair Loss: Taxotere Baldness Lawyers For  Permanent Hair Loss Lawsuits Have you received Taxotere for breast cancer? Taxotere can result in hair loss or baldness  that is permanent. Taxotere  is a chemotherapy drug used for the treatment of breas...

Medical Device Lawsuits

  • File An IVC Filter Lawsuit: Our IVC Filter lawyers are filing IVC Filter lawsuits for injury and Death from a fractured migrating IVC Filter part. The IVC Filters, also known as blood clot filters, Blood Clot Capture Filters and Inferior Vena Cava Filters, are implant...

Posts Tagged ‘Arlington’

Stryker Femoral Heads Hip Replacement Lawyers

Written by lisaspitzer on . Posted in Class MDL Class Action News, Stryker femoral head hip Implant lawyer

Stryker V40 Taper Hip Replacement Lawyers Stryker Hip Replacement Lawyers

Hip Implant lawyers are filing hip replacement lawsuits for V40 Femoral head failure in the Stryker Hip Implant. In August 2016, Stryker contacted implanting physicians about metal wear associated with its V40 Taper when used with some cobalt chromium heads.Stryker Orthopaedics sent an Urgent Medical Device Recall Notification to orthopedic surgeons. The recall involves certain sizes of LIFT™ Anatomic CoCr V40™ Femoral Heads manufactured prior to 2011. If you had a LIFT- V40 Femoral Head implanted during total hip replacement, you should be watching for a letter from your surgeon in the next few weeks. You may also be getting a letter from Stryker or a company hired by Stryker to handle claims.

 Stryker Recall Metal V 40 Femoral Heads Lawsuits

Stryker has voluntarily recalled some of their metal V40 femoral heads used with hip implants. Stryker hip replacement lawyers are interested in speaking to anyone with a failed: Exeter, Citation, Meridian, Reliance, Definition, Restoration, Accolade Rejuvenate ABG 2 stems.

This failure may be due to the problems with the V40 femoral head.

The failure of these heads is caused by corrosion and metal debris at the junction between the metal head and neck. The clinical results for patients include pain, loss of mobility, ambulation problems and an inability to work. Poisoning of the soft tissue, muscle and bone are the cause. Revision surgeries may be needed due to premature failures. Stryker lawyers  are seeking patients with  LFit V40 femoral heads made before 2011.

What Is The Femoral Head  Problem?

This is a ball for total hip replacements that can be attached to hip stems, including the Accolade TMZF, Accolade 2, Meridian, and Citation. There have been numerous incidents  of taper lock failures on LFit V40 femoral heads made before 2011,  This taper lock connects the “ball” part of the hip joint to the  hip stem that is inserted in the femur. When it breaks the femoral head will detach from the femoral neck.

Get A Stryker Hip Implant Lawyer

Our Stryker Hip Replacement lawyers are currently accepting Stryker LFit V40 failure cases.

Hip Replacement Helpline Launched

Written by lisaspitzer on . Posted in Biomet Hip Replacement lawyers, DePuyPinnacle- ASR Hip Replacement lawyers, encore hip replacement lawyers, Medical Device Lawsuits, Omnilife Hip Replacement lawyers, Smith amd Nephew Hip Replacement Lawyers, Wright hip Replacement lawyers

Hip Replacement Lawsuits

Many 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 Lawsuits

Hip 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.

  1. Stryker Rejuvenate Modular Neck Cases – All
  2. Stryker ABG II Modular neck Cases – All
  3. Stryker Accolade (TMZF) Stem cases with Cobalt Chromium modular heads. These stems have the potential for significant head neck corrosion – All cases with Metallosis.
  4. Wright Medical Conserve Cup (MOM) cases – ALL
  5. 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.
  6. Depuy ASR – ALL
  7. Depuy Pinnacle Metal on Metal (MOM) with modular heads greater than 36 mm.
  8. Zimmer Durom Cup cases with modular heads greater than 36 mm.
  9.  Zimmer M/L Taper Kinectiv Stem cases (this is their Modular neck design)- All cases with Metallosis.
  10.  Biomet M2A 38mm / Magnum MOM cases. ALL cases with Metallosis.
  11.  DJO / Encore MOM hip cases. All cases revised due to Metallosis.
  12.  Omnilife Apex Arc – This is a smaller manufacturer but this device is a mixed metal modular neck device. ALL
  13.  Smith & Nephew R3 (MOM) cup cases. Only cases that have metallosis and were revised or need a revision.
  14. 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.

Knee Replacement Lawyers For Knee Replacement Lawsuits

Written by lisaspitzer on . Posted in Smith & Nephew's OXINIUM devices lawyer, Stryker’s Scorpio implant lawyers, Zimmer’s NexGen Natural Knee System implant lawyers

Knee replacement lawsuits are being filed for
  • Zimmer’s NexGen Natural Knee System implant lawyers,
  • Stryker’s Scorpio implant lawyers,
  • Smith & Nephew’s OXINIUM devices lawyer.

Knee Replacement Complications

Complications Lawsuits are Being Filed For: Persistent pain, swelling or stiffness, Deep vein thrombosis, Implant failure within five years, Nerve injuries, Fracturing, chipping and migration and Infections.

Brand Knee Replacements Lawsuit Filings

Knee Replacements Causing Problems Include: DePuy knee, Zimmer NexGen LPS, CR and MIS, Natural Knee System, Stryker Scorpio CR and PS components, Duracon Total Knee, Unicompartmental Knee System, Smith & Nephew Oxinium Genesis II and Profix II, Journey Uni Tibial Baseplate, and Biomet Vanguard CR.

Knee Replacement Recalls

Has your  knee replacement caused debilitating side effects? Have you needed  to undergo revision surgery  to fix or replace the device or to correct complications caused by the device?

Complications  resulting  in a  knee replacement recall include:

Persistent pain of recipient, Infection or drainage, Swelling or inflammation, Damage to surrounding bone, muscle, or nerves

Zimmer NexGen Knee Recalls

While there has not been a total recall on any Zimmer NexGen knee replacement devices, a number of device components have been recalled. In 2010, Zimmer NexGen MIS Tibial Components were recalled due to high incidences of failure associated with the components. The Zimmer NexGen LPS-Flex GSF Femoral Component was also recalled due to evidence of loosening. Additionally, the Zimmer Natural-Knee II Durasul Patella faces a Class II recall. This component is not part of the Zimmer NexGen product line.

Zimmer Recalls

Zimmer NexGen knee recalled components include: NexGen MIS Tibial Components,NexGen TM Tibial Trays, NexGen LPS-Flex GSF Femoral Component, NexGen MIS Modular Tibial Plates and Keels.

Stryker Knee Replacement Recalls

In April 2013, the FDA issued a Class I recall of Stryker’s ShapeMatch Cutting Guide.  The Guides help to position knee replacement components and guide the marking of the patient’s bone prior to cutting. In November 2012, Stryker acknowledged manufacturing defects in the ShapeMatch Cutting Guide and instructed surgeons to discontinue use. This knee replacement recall was because  the software has a defect that causes wider cutting ranges. As a result, knee replacement patients may experience severe complications such as instability of the joint, fracture, chronic pain, and mobility limitations. Patients may also require the need for revision surgery.

Other Knee Replacement Recalls

StrykerDuracon Total Knee, Unicompartmental Knee System, Scorpio PS and CR components, BiometVanguard CR, Smith & Nephew Journey Uni Tibial Baseplate, Oxinium Genesis II and Profix II

Get a Knee Replacement Lawyer

Bard IVC Filter Lawyers | Bard Inferior Vena Cava Filter Alert

Written by lisaspitzer on . Posted in Bard IVC Filter Lawyers, Cook IVC Filter Lawyer, Medical Device Lawsuits

File A Bard IVC Filer Lawsuit For A Failed Bard Inferior Vena Cava Filter

Bard IVC Filter Dangers

Bard  IVC Filters have  certain dangers. The filters can fracture and pieces can migrate and perforate various organs in the body.  Inferior Vena Cava filters are implanted to capture blood clots before they can settle in the brain or lungs resulting in a pulmonary embolism or stroke.

Bard IVC Filter Lawyers Filing Inferior Vena Cava Lawsuits For a Failed

  • Bard Recovery filter;
  • Bard G2 filter;
  • Bard G2 Express filter;
  • Cook Gunther Tulip

Vena Cava Filter Lawsuits Filed

What are the Complications Of The Bard  IVC Filters?

Fracture of the Cook  IVC Filter, Bard IVC Filter Migration, Perforation, Puncture or Serious Damage to the Heart, Lungs or Vena Cava, Internal Bleeding, Hematoma or Nerve Injury at the Puncture Site of the Bard IVC Filter, Inferior Vena Cava Filter related Pulmonary Embolism, Respiratory Distress From the IVC Filter, Infection from the IVC Filter, Shortness of Breath, Death

Get a Bard Inferior Vena Cava Filter Lawyer   File Your Bard  IVC Filter Lawsuit

Texas Vena Cava Filter Lawyers, Blood Clot Filter Attorneys

Written by lisaspitzer on . Posted in Atlanta, Baltimore, Bard IVC Filter Lawyers, Biloxi, Blood Clot Filter lawyer, Boca Raton, Boston, Charleston, Charlotte, Dallas, Denver, Detroit, Fort Lauderdale, Houston, Los Angeles, Louisville, Macon, Medical Device Lawsuits, Miami, Minneapolis, NYC, Philadelphia, Phoenix, Provo, Texas Multidistrict Litigation Lawyers

Get A Texas Vena Cava Filter Lawyer

IVC Filter Lawyers

Blood Clot Filter Lawyer

Dallas, Houston, Abilene, Amarillo, Austin, Arlington, Beaumont, Brownsville, College Station, Corpus Chrisit, Del Rio, Denton, EL Paso, Fort Worth, Galveston, Houston, Huntsville, Killeen, Laredo, Lubbock, Mcallen, Odessa, San Antonio, San Marcos, Tylor, Victoria, Waco, and Wichita Falls Vena Cava Filter, Blood Clot Filter, IVC Filter Lawyers.

What Is A Blood Clot Filter?

The  Vena Cava Filters are implanted in patients to capture blood clots before they can become lodged in the brain or lungs. This is used for patients who cannot tolerate blood thinners. The blood clot is captured to avoid traveling and causing a stroke or pulmonary embolism.

Manufacturers  IVC Filters  Lawsuits Being Filed

MDL’s or multi district litigations have been formed for both the Bard and Cook IVC Filters

C.R. Bard IVC Filters

  • Recovery IVC Filter (withdrawn in 2005),
  • G2 IVC Filter,
  • G2 Express,
  • G2X Filter,
  • Eclipse,
  • Meridian
The U.S. Judicial Panel on Multidistrict Litigation (JPML) has centralized all Bard blood clot filter lawsuits into (MDL No. 2641, In Re: Bard IVC Filters Products Liability Litigation) in Arizona under U.S. District Judge David G. Campbell.

Cook IVC Filters

  • Günther Tulip,
  • Celect
The Judicial Panel on Multidistrict Litigation (JPML) has consolidated all Cook blood clot filter lawsuits in the Southern District of Indiana, assigned to Judge Richard L. Young and Magistrate Judge Tim A. Baker. These cases allege defective design, misrepresentation in marketing, and failure to warn doctors and patients.

Other Retrievable IVC Filters

  • B. Braun TempoFilter IVC filter,
  • B. Braun VenaTech,
  • Rex Medical (Argon Medical) Option IVC filter,
  • ALN Optional Vena Cava Filter,
  • Crux Vena Cava Filter (VCF)-

Blood Clot Filter Dangers

Blood clot filters have serious side effects including vein and organ perforation, migration and breakage. Broken pieces of the Blood Clot Filters can travel through the body, damaging organs.

These Severe Injuries Can Result In:

Death, Hemorrhaging, Pulmonary Embolism, Stroke,

IVC Filter Lawsuits Are Being Filed

If you are a victim of an IVC Filter with serious or life threatening side effects or have lost a loved one due to a faulty blood clot filter contact our Vena Cava Filter Lawyers today.

IVC filters may cause the following severe complications:

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

File Your Vena Cava Filter Lawsuit

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.

Were You Or A Loved One Injured Because

Parts of the IVC Filter  broke  lose Moved or migrated Punctured or perforated organs Became  lodged in the wrong part of the body Blocked  blood vessels Became  wedged in the body

Speak to a Blood Clot Filter Lawyer Now

Resperdal Class Action Lawyers, Resperdal Lawsuit Helpline

Written by lisaspitzer on . Posted in Alabama Multidistrict Litigation Lawyers, Arizona Multidistrict Litigation Lawyers, Arkansas Multidistrict Litigation Lawyers, California Multidistrict Litigation Lawyers, Colorado Multidistrict Litigation Lawyers, Delaware Multidistrict Litigation Lawyers, Drug Lawsuits, Florida Multidistrict Litigation Lawyers, Georgia Multidistrict Litigation Lawyers, Indiana Multidistrict Litigation Lawyers, Kansas Multidistrict Litigation Lawyers, Massachusetts Multidistrict Litigation Lawyers, Michigan Multidistrict Litigation Lawyers, Minnesota Multidistrict Litigation Lawyers, Missouri Multidistrict Litigation Lawyers, Montana Multidistrict Litigation Lawyers, New Jersey Multidistrict Litigation Lawyers, New Mexico Multidistrict Litigation Lawyers, New York Multidistrict Litigation Lawyers, Ohio Multidistrict Litigation Lawyers, Resperdal lawsuits

Risperdal Lawyers Filing Gynecomastia Lawsuits

If you or a loved one was prescribed Risperdal as a teenage boy and now have enlarged breasts, developed female type breasts and /or been diagnosed with Gynecomastia,  contact Class Action Lawyer Network  Risperdal Injury Lawyers today to discuss your options in a Risperdal lawsuit.

Our Resperdal lawyers are reviewing cases for young  boys diagnosed with gynecomastia or male breasts after using Risperdal. Problems may result in:

  •     Breast Growth Among Boys
  •     Puffy Nipples or Enlarged Nipples
  •     Galactorrhea (production of milk from breasts)
  •     Painful Breasts or Nipple Discharge
  •     Mastectomy or Gynecomastia Surgery to Remove Male Breasts
  •     Gynecomastia (growth of male breasts, which may be painful or tender)

If your son has been diagnosed with Gynacomastia call our Resperdal helpline and speak to our trained medical social worker today.

Rispedral Side Effects In Male Children

Risperdal (risperidone) is an antipsychotic manufactured by Johnson & Johnson. It  was originally approved by the FDA for use for adults with schizophrenia.  Risperdal has also been widely used by children for bi-polar disorders, autism, irritability, aggression and behavior disorders.

Speak To A Risperdal Lawyer

The Riserdal  lawyers are reviewing cases for Risperdal breast growth among boys.

Children Are Being Injured By Risperdal

Lawsuits are being filed  for  abnormal development of large mammary glands among boys and adolescents, resulting in breast development.  Surgery has been  necessary to remove the breasts caused by the Risperdal gynecomastia.  This has caused emotional trauma for boys and young adult males and some incidents of suicide. Parents throughout the United States are pursuing a Rispedal lawsuit on behalf of kchildren  who developed breasts on Risperdal.

Lawsuits allege that Johnson & Johnson failed to adequately research the effects of their medication or warn about the connection between Risperdal and breast growth.

Risperdal Lawsuit Update

Although Resperdal is not currently an MDL, settlements for Risperdal breast growth have been reached by Johnson & Johnson in lawsuits bellwether trials where a number of cases are presented to juries to test the potential settlements and outcomes. Do not delay. Call no to discuss a Resperdal lawsuit.
 

 

 

Nationwide Bladder Sling Lawyer Outreach, Bladder Sling Lawsuits Being Filed

Written by lisaspitzer on . Posted in Class MDL Class Action News

Bladder Sling Lawyers, Bladder Sling Lawyers Filing Nationwide Bladder Sling Lawsuits

The bladder sling lawyers of Class Action Lawyer Network are accepting all nationwide bladder sling lawsuits. Lawsuits are being filed as a part of the consolidated MDL'S in West Virginia.

What Is A Bladder Sling?

Bladder slings are used to treat urinary incontinence by implanting  a sling around the urethra. The bladder sling is attached to the abdominal wall or pelvic bone. The bladder sling is a vaginal mesh device, and has all the complications for which TVT lawsuits are being filed.

Bladder Sling Complications

Erosion thru the vaginal wall 

Erosion into the bladder,

Pain during sexual intercourse,

Bleeding,

Infection,

Perforation of bladder, colon,

Urinary incontinence

Problems voiding.

Our bladder sling lawyers are  filing bladder sling lawsuits for  women. You must file a bladder sling lawsuit quickly, as the statute of limitations is running very close in many states.

 The manufacturers are:

    Bard Avaulta Support System MDL No. 2187

    AMS Elevate Prolapse Repair System MDL No. 2325

    AMS Apogee Vault Suspension System

    AMS Perigee System

    AMS Monarc Sling System

    AMS Sparc Sling System

    Ethicon Gynecare Gynemesh MDL No. 2327

    Ethicon Gynecare Prolene Soft Mesh

    Ethicon Gynecare Prolift Pelvic Floor Repair System

    Ethicon Gynecare TVT Transvaginal Sling

    Boston Scientific Pinnacle Pelvic Floor Repair Kit MDL No.2326

    Boston Scientific Uphold Vaginal Support System

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 No. 2187 | In RE: CR Bard, 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
 

Our experienced bladder sling lawyes ready to file bladder sling lawsuits  slings problem lawsuits.  Vaginal mesh products have many different names. Do not assume your bladder sling is not covered in the TVT lawsuits  until you speak to one of our bladder sling  lawyers. Many states have a  statue of limitations issue. Time is of the essence. Call our nationwide bladder sling lawyers today.

Did You Take Yaz Or Yasmin? Settlements For Yaz Lawsuits For Bloodclots

Written by lisaspitzer on . Posted in Class MDL Class Action News

Yaz, Yasmin Lawsuit  Multidistrict Litigation


MDL 2100 – Yasmin and YAZ (Drospirenone) Marketing, Sales Practices and Products Liability Litigation, multidistrict litigation (MDL) in Illinois federal court.


Yaz lawyers are accepting Yaz lawsuits for blood clot related injuries:

  • Pulmonary Embolism
  • Blood Clots
  • Stokes
  • Deep Vein Thrombosis

Bayer is facing thousands of Yaz and Yasmin lawsuits involving blood clot related injuries.

Yaz Blood Clot Settlements

According to Bayer’s 2nd Quarter 2013 Statement, Bayer  haa agreed to pay more than $1.4 billion to resolve an estimated 6,700 lawsuits from women  who suffered a:
    Heart attack or Stroke from Yaz or Yasmin
    Pulmonary Embolism from Yaz or Yasmin
    Deep Vein Thrombosis from Yaz or Yasmin

There are still  more than 5,000 additional claims involving a thrombosis blood clot related injury.  Bayer is continuing negotiating on a case-by-case basis, after complete documentation and presentation of the claim by an attorney. It is not too late to file your Yaz blood clot lawsuit. Our Yaz lawyers are still  continuing to review and evaluate potential claims from women who suffered a pulmonary embolism, deep vein thrombosis, heart attack, stroke or other blood clot injury while using Yaz, Yasmin or Ocella.

If you or a loved one has been injured by Yaz or a loved one has died from a Yaz related injury call us for a Yaz lawyer today.
 

Tylenol Lawsuits For Liver Damage Multi District Litigation Consolidation

Written by lisaspitzer on . Posted in Tylenol Liver Damage Lawyers, Tylenol Liver Failure Lawsuit News

Class Action Lawyer Network Tylenol liver damage lawyers report that tylenol liver failure  lawsuits will be centralized in a multidistrict litigation in Pennsylvania  Federal Court,

Tylenol Lawsuit Consolidated In Pennsylvania

All Tylenol liver damage  lawsuits filed against McNeil-PPC, Perrigo, Novartis and others have  been consolidated under multidistrict litigation in the Eastern District of Pennsylvania to facilitate the pretrial proceedings for  these cases

The U.S. Judicial Panel on Multidistrict Litigation (MDL) has ruled that 27 Tylenol liver damage lawsuits filed against  the manufacturers of tylenol related products will be consolidated under Tylenol Lawsuit MDL 2436 in the Eastern District of Pennsylvania.
All of the cases conslidated in MDL 2436 involve liver damge related injury or wrongful death. These  claims alledged that use of over-the-counter (OTC) Tylenol (generically acetaminophen) caused the victims to suffer from serious liver damage or  liver failure.

Call Class Action Lawyer Network's Tylenol Liver Damage Lawsuit Department Today.

The MDL  Judicial Panel feel that the  allegations of liver injury associated with the use of OTC Tylenol, the cases share factual issues regarding the design, manufacture, labeling, marketing and sale of Tylenol. Consequently, the centralization of these cases in the Eastern District of Pennsylvania would eliminate duplicative discovery facilitate the proceedings.

Class Action Lawyer Nwtwork  attorneys  have decades of collective dangerous drig  and device lawsuit experience,

If you or a loved one has suffered liver damage or liver failure while taking Tylenol call us to discuss a Tylenol liver damage lawsuit or Tylenol liver failure lawsuit.

Tylenol Liver Damage Lawsuit Criteria

Have you or a loved one been diagnosed with Liver Failure, liver damage from taking Tylenol? Do you have a clean medical history of any liver problems such as: Liver cancer, liver mass, Autoimmune Hepatitis, Alcoholic Cirrhosis,Primary Sclerosing Colangitis, Wilson’s disease, or Budd Chiari Syndrome  and yet,  now have liver damage after taking Tylenol?
Our Tylenol liver damage lawyers are accepting Tylenol liver failure cases  if  the liver failure results in hospitalization, liver transplant, or liver transplant waiting list or death. If you meet this criteria we would like to speak to you regarding filing a Tylenol liver damage or liver failure case.

Class Action Lawyer Network  accepting Tylenol liver damage lawsuts  or liver failure  lawsuits for individuals who experienced  any of the following within a week after taking  an acetaminophen medication such as Tylenol:

  •     Hospitalization Due to Severe Liver Injury or Liver Problems
  •     Diagnosed with Liver Failure
  •     Liver Transplant or Placed on Waiting List for Liver Transplant
  •     Death from Liver Failure

Tylenol Liver Damage Lawyers, Tylenol Liver Failure Lawsuits

Written by lisaspitzer on . Posted in Class MDL Class Action News, Drug Lawsuits, Drug Warnings, Florida Multidistrict Litigation Lawyers, Tylenol Liver Damage Lawsuits, Tylenol Liver Damage Lawyers, Tylenol Liver Failure Lawsuit News

Tylenol Liver Damage Lawyers of Class Action Lawyer Network Are Filing  Nationwide Tylenol Liver Failure  Lawsuits

The Tylenol liver damage lawyers of Class Action Lawyer Network are accepting nationwide lawsuits for you , your loved one or child who has suffered liver damage from Tylenol. Our Tylenol Liver Damage Helpline is helping victims of liver damage from Tylenol.

The Tylenol Liver Damage Facts

It is now known that Tylenol can result in acute liver failure and death. Statistics have shown taht  Tylenol is the leading cause of acute liver failure in the United States; nearly half of U.S. incidents of acute liver failure are caused by  taking too much acetaminophen. Acetaminophen is anactive ingredient in Tylenool.  Call our Tylenol liver failure  helpline to speak to lawyers help who are filing liver damage lawsuits for victims  of Tylenol who have been diagnosed with Tylenol liver damage or failure.

Symptoms Of Liver Damage

  •     Discolored skin and eyes that appear yellowish
  •     Abdominal pain and swelling
  •     Itchy skin that doesn't seem to go away
  •     Dark urine color
  •     Pale stool color
  •     Bloody or tar-colored stool
  •     Chronic fatigue
  •     Nausea
  •     Loss of appetite
     

Class Action lawyers For Tylenol Liver Failure

  • Tylenol's manufacturer lowered the safe maximum dosage from 4000 mg to 3000 mg per day.
  • Tylenol liver Failure Helpline lawyers are fighting for justice for victims of tylenol Llver damage and liver failure
  • If you or a family member has  been diagnosed with  severe liver damage or acute liver failure from excessive use of Tylenol or other over the counter medications that contain acetaminophen the Tylenol liver damage helpline is here for you.
  • People who have experienced acute liver failure or serious liver damage related to Tylenol use may file a Tylenol liver damage lawsuit  lawsuit

Tylenol Lawsuit Multi District Litigation Has Formed

The  Tylenol injury lawsuits have now been centralized as part of multidistrict litigation in federal district court in Pennsylvania.

The lawsuits filed alledge a strong link between acetaminophen and liver failure. Lawsuits are  alleging that acetaminophen in various Tylenol products was responsible for users’ severe liver damage.

Tylenol Liver Damage Lawsuit Criteria

Have you or a loved one been diagnosed with liver Failure, liver damage or a severe liver injury from taking Tylenol?

Our Tylenol liver damage lawyers are accepting Tylenol liver failure if  the liver failure results in hospitalization, liver transplant, liver transplant waiting list or death. If you meet this criteria we would like to speak to you regarding filing a Tylenol liver damage lawsuit where there is no prior medical history of liver damage or any liver damage related medical conditions.
 

Call our Tylenol Liver Damage Helpline to file your liver damge lawsuit.