Posts Tagged ‘new orleans’
Stryker V40 Taper Hip Replacement Lawyers Stryker Hip Replacement LawyersHip 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 LawsuitsStryker 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 LawyerOur Stryker Hip Replacement lawyers are currently accepting Stryker LFit V40 failure cases.
Hip Replacement LawsuitsMany 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 LawsuitsHip 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.
- Stryker Rejuvenate Modular Neck Cases – All
- Stryker ABG II Modular neck Cases – All
- Stryker Accolade (TMZF) Stem cases with Cobalt Chromium modular heads. These stems have the potential for significant head neck corrosion – All cases with Metallosis.
- Wright Medical Conserve Cup (MOM) cases – ALL
- 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.
- Depuy ASR – ALL
- Depuy Pinnacle Metal on Metal (MOM) with modular heads greater than 36 mm.
- Zimmer Durom Cup cases with modular heads greater than 36 mm.
- Zimmer M/L Taper Kinectiv Stem cases (this is their Modular neck design)- All cases with Metallosis.
- Biomet M2A 38mm / Magnum MOM cases. ALL cases with Metallosis.
- DJO / Encore MOM hip cases. All cases revised due to Metallosis.
- Omnilife Apex Arc – This is a smaller manufacturer but this device is a mixed metal modular neck device. ALL
- Smith & Nephew R3 (MOM) cup cases. Only cases that have metallosis and were revised or need a revision.
- 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.
- Zimmer’s NexGen Natural Knee System implant lawyers,
- Stryker’s Scorpio implant lawyers,
- Smith & Nephew’s OXINIUM devices lawyer.
Knee Replacement ComplicationsComplications 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 FilingsKnee 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 RecallsHas 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 RecallsWhile 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 RecallsZimmer 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 RecallsIn 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 RecallsStrykerDuracon 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 DangersBard 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
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 PowderAlthough 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 SettlementsA $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.
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.
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.
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