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.
If you have kidney failure after taking Nexium or Prilosec contact our Nexium- Prilosec Lawsuit Helpline.
If you have a diagnosis of kidney disease and proof that you were taking Nexium, Prilosec or other acid reflux- proton-pump inhibitor medications for extending periods we can help. Lawsuits are being filed by our Nexium- Prilosec Kidney Disease lawyers.
Proton Pump Inhibitor Lawsuits Filed
Nexium, Aciphex, Protonix, Prevacid, Zegerid,omeprazole, Dexilant, Prilosec, omeprazole
Kidney Side Effects of Proton Pump Inhibitor drugs:
Kidney Failure Lawyer
Chronic Kidney Failure,
Acute Kidney Failure,
Acute Interstitial Nephritis,
Dialysis Treatment, and
Kidney Removal or Transplant Surgery
Symptoms Of Kidney Disease:
Nausea and vomiting, Passing only small amounts of urine, Swelling, particularly of the ankles, and puffiness around the eyes, Unpleasant taste in the mouth and urine-like odor to the breath,
Persistent fatigue or shortness of breath, Loss of appetite,Increasingly higher blood pressure, Muscle cramps, especially in the legs, and Pale skin, Excessively dry, itchy skin.
Get a Nexium or Prilosec Helpline lawyer
Our extensive bleeding blood thinner lawyers are accepting Eliquis and Xarelto cases for extenive bleeding injury and wrongful death claims.
Eliquis is a blood thinner that is similar to Pradaxa, and Xarelto. The problem appears to be once bleeding begins it is very difficult to control. This can result in severe internal bleeding and bleeding that results in fatal injury.
Eliquis Injury Lawsuits Filed For:
Wrongful Death from extensive bleeding
There is currently no reversal agent for Eliquis internal bleeding.
If you have lost a loved one due to extensive bleeding from Eliquis contact our Blood thinner class action lawsuit department today
The hip and knee lawsuit attorneys at Class Action Lawyer Network are accepting:
Faulty Hip Replacement Lawsuits for :
- DuPuy ASR,
- Zimmer MMC,
- DePuy Pinnacle (metal on metal),
- Wright Medical Conserv,
- Stryker Rejeuvenate or ABG11,
- Stryker Accolade/Citation/ Meridian,
- Encore Metal on Metal
Faulty Knee Replacement Lawsuits For :
Zimmer Persona Knee
Knee Implant Failure Complications: dislocation, early joint breakdown due to poor design infection, and loosening at the knee joint,
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 breast cancer. Taxotere has been shown to cause permanent hair loss. Taxotere lawyers are filing permanent hair loss lawsuits against the manufacturer of Taxotere, Sanofi-Aventis. The U.S. Food and Drug Administration has acknowledge that Taxotere can result in permanent hair loss, and this warning will now be placed on the Taxotere label.
If you or a loved one has been a victim of permanent hair loss from Taxotere contact a Taxotere class action lawyer today
Power Morcellator Lawyers Filing Lawsuits
Power Morcellator Device Spreads Uterine Cancer Continue To Grow
Morcellator lawyers advise that power Morcellator lawsuits have been consolidated by the Judicial Panel on Multidistrict Litigation. 2652 cases have been filed for women who underwent laparoscopic power morcellation for hysterectomies or myomectomies and were put at risk for spreading previously hidden cancer cells.
- The Morcellator has jaw-like blades that rapidly spin to shred fibroid tissue so that the pieces are able to be removed from the body.
- It is now known that as tool does this, it uncovers and disseminates uterine sarcoma cells.
- The FDA issued a safety warning against laparoscopic power morcellation procedures due to the risk of spreading cancer.
- Many women have developed serious or fatal leiomyosarcoma.
- There have been deaths of “hundreds, if not thousands of women in America”.
Morcellator lawyers at Class Action Lawyer Netowork are accepting cases for women who have undergone power morcellation and who has subsequently been diagnosed with cancer.
Invokana lawyers are filing Invokana lawsuits for Ketoacidosis, heart attack, diabetic coma and deaths.
Invokana is an SGLT2 inhibitor that may lead to ketoacidosis. The FDA has issued warnings that
Have been shown to cause serious medical conditions including:
The Invokana lawyers at Class Action Lawyer Network are filing lawsuits on behalf of patients who suffered serious injuries after taking:
Xigduo XR (dapagliflozin/metformin)
The FDA Issued A Warning For Invokana
In May 2015, the FDA warned that Invokana may put patients at risk for ketoacidosis. Ketoacidosis may cause diabetic comas or death.
The Dangers Of Invokana Resulting In Lawsuits
Our Invokana lawyers are filing lawsuits claiming the manufacturer failed to warn patients and doctors of the risks of kidney failure, myocardial infarction, and ketoacidosis Invokana os a medication given to diabetics to help lower blood sugar.
Invokana Class Action Lawyers
Our Invokana lawyers are filing Invokana lawsuits for kidney damage,heart attacks, and ketoacidosis complications from the medication Invokana. Lawsuits are being filed because the manufacturers and of SGLT2 inhibitors (such as Johnson & Johnson, Janssen Pharmaceuticals Inc., AstraZeneca & Boehringer Ingelheim) failed to warn patients and physicians of the risks of kidney failure, myocardial infarction and ketoacidosis.
What is Invokana?
You may have been prescribed Invokana to improve glycemic control and lower blood sugar if you are a type 2 diabetic. These medications lower a person’s blood sugar by causing the kidneys to remove it through the urine.
Heart Attack Ketoacidosis Drugs
Canagliflozin and Metformin,
Dapagliflozin and Metformin extended-release,
Empagliflozin and Linagliptin.
Risks Alert For Kidney Failure
Kidney failure occurs when your kidneys stop functioning. When your kidneys stop properly functioning, you will experience cause weakness, shortness of breath, lethargy, confusion, abnormal heart rhythms and even sudden death.
Risk Alert For Heart Attacks
A heart attack results in the death of cells within the heart. This is caused by a restriction of blood. It occurs when there is a blockage in the arteries preventing blood from reaching portions the heart.
Risk Alert For Ketoacidosis
Ketoacidosis is high levels of ketones. Ketoacidosis can result in a patient suffering a diabetic coma, extended hospitalization and even death. The FDA warns that SGLT2 inhibitors for diabetes may result in a serious condition of too much acid in the blood. Medications in the class include AstraZeneca’s Farxiga and Xigduo, Jardiance and Glyxambi from Lilly and Boehringer Ingelheim. J&J also combines the active ingredient in Invokana with metformin and markets it as Invokamet.
Speak to one of our Invokana lawyers today
Class Action Lawyer Network lawyers are now accepting
Benicar Gastrointestinal Damage Lawsuits
Bard Blood Clot Vena Cava Fracture Lawsuits
Zocar Kidney Failure Lawsuits
Xarelto Extensive Bleeding Lawsuits
GranuFlo Dialysis Medication- Immediate Heart Attack Lawsuits
The lawyers of Class Action Lawyer Network are always up to date on all the current drugs and devices harming patients or with knew FDA warnings.
What Is Benicar? What Is The Benicar Lawsuit?
Benicar is a blood-pressure medication that has been linked to gastrointestinal injury including sprue-like enteropathy. This disease causes chronic diarrhea and weight-loss. The lining of the intestine is no longer able to absorb nutrients due to the lining damage from this medication. Benicar lawsuits have been filed for people with this severe side effect.
What Is The Bard Vena Cava? What Is The Bard Vena Cava Lawsuit?
The Bard IVC filters are designed to capture blood clots before they enter the lungs. These filters have fractured and fragments have migrated puncturing internal organs and veins.
Surgeons have implanted the inferior vena cava filter in the veins of patients to prevent blood clots from moving into the lungs. The filters capture the clots in the blood stream. Reported adverse incident complications include punctured organs, blood vessels and filter migration to different parts of the body.
IVC Filter Lawsuits Filed
The Bard Recovery filter
The Bard G2 filter
The Bard G2 Express filter
What Is Zocar? What Are The Zocar Lawsuits For?
Zocor is a cholesterol drug and is prescribed to many people with high cholesterol. Zocar has warnings for Zocor liver damage and muscle damage. Lawsuits are being filed for liver damage and liver damage death from Zocar
What Is Xarelto? What Are The Xarelto Lawsuits For?
Xarelto (rivaroxoaban) is an anticoagulant prescribed to reduce the risk of stroke, deep vein thrombosis (DVT), pulmonary embolism (PE) and blood clots. injuries. It is prescribed to people with non-valvular atrial fibrillation and following knee and hip replacement surgery to prevent blood clots.
Xarelto Extensive Bleeding Lawsuits Are Being Filed For:
Gastrointestinal bleeding- bleeding ulcers,
Brain Hemorrhage and Deaths
What Is GranuFlo?
Granuflo dry concentrate and NaturaLyte liquid concentrate are among the most widely used products during hemodialysis treatment.
What Are GranuFlo Dialysis Medication Lawsuits Filed For?
Sudden MI or heart attack
Class Action Benicar lawyers announce a new Benicar lawsuit helpline because the number of Benicar lawsuits in the multidistrict litigation, as of July 15, 2015, has reached 915 lawsuits. The lawsuits are against the makers of Benicar, Daiichi Sankyo, Inc., its parent company, Daiichi Sankyo Co. Ltd., and Forest Laboratories Inc. Benicar is a drug prescribed to patients with high blood pressure and has been noted to cause the development of sprue-like enteropathy. This is a severe gastrointestinal condition with symptoms such as chronic diarrhea, nausea and vomiting, and significant weight loss and malnutrition.
Benicar was approved by the FDA in April 2002. In July 2013 the FDA issued a Safety Warning for Benicar after reviewing data submitted by the Mayo Clinic. The data showed that Benicar may be associated with sprue-like enteropathy. The first lawsuits against Daiichi Sankyo were filed soon after the FDA issued the warning. This multidistrict litigation, formed in April 2015, is based in the US District Court in New Jersey.
Benicar lawyer are interested in representing individuals with these symptoms as the result of taking Benicar.
For more information on Benicar, or if you believe you have been injured by using Benicar, speak to one of our qualified Benicar attorneys.