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Medical Device Lawsuits

  • Zimmer Hip Replacement Lawyers: Network Zimmer Hip Replacement  Lawyer Win $2 Million Against Zimmer Hip Replacement Do You Have A Faulty Zimmer M/L Taper Hip Prothesis With Connective Technology and Cobalt Chromium Head? Do You Have Have Metallosis or Chromium Cobalt T...

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Zimmer Hip Replacement Lawyers

Written by lisaspitzer on . Posted in Chromium cobalt toxicity, Medical Device Lawsuits, Zimmer hip replacement lawyer

Network Zimmer Hip Replacement  Lawyer Win $2 Million Against Zimmer Hip Replacement

Do You Have A Faulty Zimmer M/L Taper Hip Prothesis With Connective Technology and Cobalt Chromium Head?

Do You Have Have Metallosis or Chromium Cobalt Toxicity?

A judge in Florida has found that Zimmer Orthopedics manufactured and marketed a hip replacement implant which has an “unreasonably dangerous design,” and has ordered the company to pay a victim  $2 million.

Zimmer Hip Replacement Lawyers

We are proud to say that the  $2 million award against Zimmer was won by a member of our lawyer network in co counsel with another attorney.

Testing Inadequate To Substantiate Safety

The testing done by Zimmer for this prothesis hip implant was inadequate to substantiate safety for the recipient.

Get a Zimmer Hip Replacement Lawyer Now

If you have a faulty Zimmer hip replacement or have high levels of chromium or cobalt in your blood stream contact us immediately for a Zimmer Hip Replacement lawyer. Zimmer Hip replacement lawyers are being filed for victims of the faulty hip replacement and people with metallosis ( Metal Toxicity ) in: we have attorneys in: Auburn AL; Birmingham AL; Dothan AL; Gadsden AL; Huntsville AL; Mobile AL; Montgomery AL; Muscle Shoals AL; Tuscaloosa AL; Anchorage AK; Fairbanks AK; Juneau AK; Flagstaff AZ; Sedona AZ; Mohave County AZ; Phoenix AZ; Prescott AZ; Show Low AZ; Sierra Vista AZ; Tucson AZ; Yuma AZ; Fayetteville AR; Fort Smith AR; Jonesboro AR; Little Rock AR; Bakersfield CA; Chico CA; Fresno CA; Humboldt County CA; Inland Empire CA; Long Beach CA; Los Angeles CA; Mendocino (new) CA; Merced CA; Modesto CA; Monterey CA; O.C. CA; Oakland CA; Palm Springs CA; Palmdale CA; Redding CA; Sacramento CA; San Diego CA; San Fernando Valley CA; San Francisco CA; San Gabriel Valley CA; San Jose CA; San Luis Obispo CA; San Mateo CA; Santa Barbara CA; Santa Cruz CA; Santa Maria CA; Siskiyou CA; Stockton CA; Susanville CA; Ventura CA; Visalia CA; Boulder CO; CO Springs CO; Denver CO; Fort Collins CO; Pueblo CO; Rockies CO; Western Slope CO; Eastern CT CT; Hartford CT; New Haven CT; Northwest CT CT; Wilmington DE; Dover DE; Newark DE; Pike Creek DE; Bear DE; Washington D.C. District of Columbia; Daytona FL; Fort Myers FL; Ft Lauderdale FL; Gainesville FL; Jacksonville FL; Keys FL; Lakeland FL; Miami FL; Ocala FL; Orlando FL; Panama City FL; Pensacola FL; Sarasota FL; Space Coast FL; St. Augustine FL; Tallahassee FL; Tampa FL; Treasure Coast FL; West Palm Beach FL; Albany GA; Athens GA; Atlanta GA; Augusta GA; Brunswick GA; Columbus GA; Macon GA; Northwest GA GA; Savannah GA; Statesboro GA; Valdosta GA; Big Island HI; Honolulu HI; Kauai HI; Maui HI; Boise ID; East ID ID; Lewiston ID; Twin Falls ID; Bloomington IL; Carbondale IL; Chambana IL; Chicago IL; Decatur IL; La Salle County IL; Mattoon IL; Peoria IL; Rockford IL; Springfield IL; Western IL IL; Bloomington IN; Evansville IN; Ft Wayne IN; INpolis IN; Kokomo IN; Lafayette IN; Muncie IN; Richmond IN; South Bend IN; Terre Haute IN; Cedar Rapids IA; Des Moines IA; Dubuque IA; Fort Dodge IA; IA City IA; Mason City IA; Ottumwa IA; Quad Cities IA; Sioux City IA; Waterloo IA; Lawrence KS; Manhattan KS; Topeka KS; Wichita KS; Bowling Green KY; Eastern KY KY; Lexington KY; Louisville KY; Owensboro KY; Western KY KY; Baton Rouge LA; Lafayette LA; Lake Charles LA; Monroe LA; New Orleans LA; Shreveport LA; Portland ME; Lewiston ME; Bangor ME; West Scarborough ME; Annapolis MD; Baltimore MD; Cumberland Valley MD; Eastern Shore MD; Frederick MD; Western MD MD; Boston Massachusetts; Cape Cod Massachusetts; South Coast Massachusetts; Springfield Massachusetts; Worcester Massachusetts; Ann Arbor MI; Battle Creek MI; Central MI MI; Detroit MI; Flint MI; Grand Rapids MI; Holland MI; Jackson MI; Kalamazoo MI; Lansing MI; Monroe MI; Muskegon MI; Northern MI MI; Port Huron MI; Saginaw MI; Southwest MI MI; Upper Peninsula MI; Duluth MN; Mankato MN; Minneapolis MN; St Paul MN; Rochester MN; St. Cloud MN; Biloxi MS; Hattiesburg MS; Jackson MS; Meridian MS; Natchez MS; North MS MS; Columbia/Jeff City MO; Joplin MO; Kansas City MO; Kirksville MO; Lake of the Ozarks MO; Southeast MO MO; Springfield MO; St. Joseph MO; St. Louis MO; Billings MT; Missoula MT; Great Falls MT; Bozeman MT; Butte MT; Grand Island NE; Lincoln NE; North Platte NE; Omaha NE; Scottsbluff NE; Las Vegas NV; Reno NV; Manchester NH; Nashua NH; East Concord NH; Concord NH; Derry Village NH; Central Jersey NJ; Jersey Shore NJ; North Jersey NJ; South Jersey NJ; Albuquerque New Mexico; Santa Fe New Mexico; Albany NY; Binghamton NY; Buffalo NY; Catskills NY; Chautauqua NY; Elmira NY; Finger Lakes NY; Glens Falls NY; Hudson Valley NY; Ithaca NY; Long Island NY; New York City NY; Oneonta NY; Plattsburgh NY; Potsdam NY; Rochester NY; Syracuse NY; Twin Tiers NY; Utica NY; Watertown NY; Westchester NY; Asheville NC; Boone NC; Charlotte NC; Eastern NC; Fayetteville NC; Greensboro NC; Hickory NC; Outer Banks NC; Raleigh NC; Wilmington NC; Winston Salem NC; Fargo ND; Akron OH; Canton OH; Ashtabula OH; Athens OH; Chillicothe OH; Cincinnati OH; Cleveland OH; Columbus OH; Dayton OH; Huntington/Ashland OH; Lima/Findlay OH; Mansfield OH; Sandusky OH; Toledo OH; Tuscarawas County OH; Youngstown OH; Zanesville/Cambridge OH; Lawton OK; OK City OK; Stillwater OK; Tulsa OK; Bend OR; Corvallis OR; East OR OR; Eugene OR; Medford OR; OR Coast OR; Portland OR; Roseburg OR; Salem OR; Allentown PA; Altoona PA; Cumberland Valley PA; Erie PA; Harrisburg PA; Lancaster PA; Meadville PA; Philadelphia PA; Pittsburgh PA; Poconos PA; Reading PA; Scranton PA; State College PA; Williamsport PA; York PA; Providence RI; Warwick RI; Cranston RI; Pawtucket RI; East Providence RI; Woonsocket RI; Charleston SC; Columbia SC; Florence SC; Greenville SC; Hilton Head SC; Myrtle Beach SC; Sioux Falls SD; Rapid City SD; Aberdeen SD; Chattanooga TN; Knoxville TN; Memphis TN; Nashville TN; Tri-cities TN; Abilene TX; Amarillo TX; Austin TX; Beaumont TX; Brownsville TX; College Station TX; Corpus Christi TX; Dallas TX; Denton TX; El Paso TX; Fort Worth TX; Galveston TX; Houston TX; Huntsville TX; Killeen TX; Laredo TX; Lubbock TX; Mcallen TX; Odessa TX; San Antonio TX; San Marcos TX; Texarkana TX; Texoma TX; Tyler TX; Victoria TX; Waco TX; Wichita Falls TX; Logan UT; Ogden UT; Provo UT; Salt Lake City UT; St. George UT; Burlington VT; Essex Junction VT; Bennington VT; Charlottesville VA; Chesapeake VA; Danville VA; Fredericksburg VA; Hampton VA; Harrisonburg VA; Lynchburg VA; New River Valley VA; Newport News VA; Norfolk VA; Portsmouth VA; Richmond VA; Roanoke VA; SouthWV VA; Suffolk VA; VA Beach VA; Bellingham WA; Everett WA; Moses Lake WA; Olympia WA; Pullman WA; Seattle WA; Spokane WA; Tacoma WA; Tri-cities WA; Wenatchee WA; Yakima WA; Charleston WV; Huntington WV; Martinsburg WV; Morgantown WV; Parkersburg WV; Southern WV WV; Wheeling WV; Appleton WI; Eau Claire WI; Green Bay WI; Janesville WI; La Crosse WI; Madison WI; Milwaukee WI; Racine WI; Sheboygan WI; Wausau WI; Cheyenne WY; Casper WY; Laramie WY; Gillette WY;

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

Risperdal Lawyers | Enlarged Breasts in Boys Lawyers

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

Our Risperdal lawyers are accepting cases for unusual breast development in males. Risperdal  $70M Verdict In Philadelphia  Risperdal  Trial Johnson & Johnson was hit with a $70 million verdict on Friday when a  Philadelphia jury found that the antipsychotic drug Risperdal had caused an adolescent boy to grow female breasts. Risperdal and Enlarged Breasts In Young  Males Risperdal   has been linked to enlarged breasts in your males. This is  a condition called gynecomastia. he Growth of male breasts can cause severe emotional distress.  Surgery may be required to correct the condition.  Risperdal may increase levels of prolactin, a hormone which stimulates breast development in women. Young boys who have taken prolactin and are displaying increased levels of this hormone may develop male breasts or gynecomastia. Can I Join The Risperdal Gynecomastia Lawsuits? If you  are a male and have  enlarged female breast call no to see if you qualify to join others in a Risperdal lawsuit. Risperdal is the  brand name for the drug called Risperidone. This is approved to treat schizophrenia and bipolar disorders. Risperdal  but has resulted in gynecomastia. Gynecomastia, the development of real female breasts.  It is real breast tissue growth caused by an increase in the hormone prolactin. If you have enlarged breasts with; Pain, Swelling, Tenderness and Nipple discharge and may need surgery  to remove excess breast tissue you may be able to join the Risperdal class action lawsuits. Get A Risperdal Lawyer Lawsuits are being filed against  Johnson & Johnson through its subsidiary Janssen Pharmaceuticals, for  failing to properly inform doctors and patients about the effects of Risperdal.  

Ovarian Cancer Talcum Powder Lawyers

Written by lisaspitzer on . Posted in Class MDL Class Action News, Consumer products Injury Lawyer, File A Talcum Powder Lawsuit

Do You Want To File A Talcum Powder Lawsuit?

If you have used talcum powder  or  baby powder products and developed ovarian cancer you may be able to file a Talcum Powder  lawsuit  Current lawsuits Johnson & Johnson claim that long-term use of talc-based products caused women to develop ovarian cancer. Victims claim   that they were not  warned of the risks associated with these talc products. Women and their families may be able to seek compensation for  ovarian cancer diagnosis  with the help of one of our lawyers.  

Is There A Risk of Talcum Powder Causing Ovarian Cancer?

Talcum powder lawsuits claim Talcum Powder  caused ovarian cancer. When used as a feminine hygiene product, talc particles can travel through the vagina and  into the ovaries and remain trapped for years. These  talc particles can cause inflammation and  eventually  lead to the growth of ovarian cancer cells.

Studies Claim Dangers Of Talcum Powder

Although Johnson & Johnson maintains that talcum powder is safe for use, plaintiffs in ovarian cancer lawsuits offer   studies that  suggest an association between talc and ovarian cancer dating as far back  as 1971. In 1994, Johnson & Johnson was put on notice of a  link between talc and ovarian cancer. A letter was sent from the Cancer Prevention Coalition to the then-CEO of the company.

Will  There Be  a Talcum Powder Ovarian Cancer Class Action Lawsuit I Can Join ?

According to news reports, more than 1,200 women claim talcum powder caused their  ovarian cancer. Currently the lawsuits are being filed at the state level.

Talcum Powder Lawsuit Settlements

A $72 million talcum powder verdict is handed down against Johnson & Johnson in favor of a woman who claimed that long-term Shower-to-Shower use for feminine hygiene caused her to develop ovarian cancer. The verdict included a $62 million award of punitive damages against the company. Our  talcum powder cancer lawyers  are available to discuss your options.    

GranuFlo Lawyers, Dialysis Medication Lawsuits

Written by lisaspitzer on . Posted in Drug Warnings, GranuFlo Dialysis Medication Lawyers

 

Dialysis Medication Lawsuits Filed For Heart Attacks

Our lawyers have been filing both Naturalyte GranuFlo Acid Concentrate and Liquid Acid Concentrate GranuFlo  recall lawsuits due  to reported immediate  heart attacks . These products are used in dialysis treatment to cleanse the blood in conjunction with a dialysis machine. Fresenius Medical Care is facing lawsuits  due  to failure to  warn the public of the GranuFlo heart attack risk when it was aware of GranuFlo has a tendency to increase bicarbonate levels to a hazardous degree.   Fresenius Medical Care is a leading provider of dialysis clinics, machines and other dialysis products.

GranuFlo Heart Attack Risks

The risk of GranuFlo heart attack (myocardial infarction) known by Fresenius Medical Care in 2011.  The GranuFlo heart attack risk was first disclosed in a Fresenius internal company memo which stated the company had made “troubling findings” related to GranuFlo heart attack death risks, and noted that, “the issue needs to be addressed urgently.”  The drug's have elevated bicarbonate levels in the bloodstream, resulting in metabolic alkalosis. Our GranuFlo heart attack risk lawyers will expain to you what the medical product lawsuits are amd review your case.

GranuFlo FDA Recall, GranuFlo FDA Warning

  • The FDA issued a GranuFlo Heart Attack Warning on May 25, 2012, 
  • Class 1 FDA GranuFlo Recall on June 27, 2012. 

 GranuFlo Lawsuits, GranuFlo Recall Lawsuits

Dilaysis medication  lawsuits are being  filed by or on behalf of persons who have had a heart attack immediately after GranuFlo was used in their dialysis treatment.

 

 

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.
 

 

 

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