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.
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 of recurrence and failure from the Physiomesh.
What Is The Physiomesh?
The Physiomesh is a hernia repair mesh made from polypropylene just like the vaginal mesh products.
The FDA originally approved Ethicon’s Physiomesh on April 9, 2010. Ethicon used the FDA 510(k) approval program for the Physiomesh. This allowed them to get it on the market fast.
Problems With The Physiomesh
Numerous studies have shown that the Physiomesh has lower incorporation strengths than the other hernia mesh products. Physiomesh coating issues were observed over time to lead to scar plate formation, but little to no abdominal wall adherence.
Physiomesh: Ethicon Hernia Mesh Lawyers
Speak to a physiomesh hernia mesh attorney to discuss a Physiomesh lawsuit
A Multi District Litigation has been requested for the consolidation of the Invokana lawsuits by Invokana lawyers as lawsuits continue to increase. A consolidation is requested to facilitate proceeding under one judge and jurisdiction.
The lawsuits against the manufacturer of the diabetes drug Invokana are alleging serious injuries after taking Invokana, including heart attack, kidney damage and a dangerous blood condition known as ketoacidosis. The lawsuits claim that Johnson & Johnson and its subsidiary Janssen failed to warn patients and doctors about the risks of taking Invokana.
Invokana lawyers filed a motion on September 20 asking the U.S. Judicial Panel on Multidistrict Litigation to consolidate Invokana lawsuits. The formation of an MDL would transfer all cases to a single judge and jurisdiction.
Invikana lawyers explained in the motion that the FDA had received many reports of kidney damage as a result of patients taking Invokana, which led the FDA to issue a stronger Invokana warning risk with a June 2016 label change. That warning was preceded by another label change in May 2015, alerting users to the risk of ketoacidosi. Ketoacidoasis can be a life-threatening condition that occurs when blood acids known as ketones reach dangerously high levels. Additional warnings were added to the label in August 2016, noting that fatal cases of ketoacidosis had been reported with Invokana use.
What Is Invokana?
Invokana is a diabetes drug in the SGLT2 inhibitor category. It regulate blood sugar levels by encouraging the body to eliminate extra glucose in urine.
Consolidation has been requested for the District Court of New Jersey in Trenton, where 36 of the Invokana lawsuits are already pending. All of those cases are before Judge Brian R. Martinotti, a federal judge the motion notes has extensive experience with complex litigation.
If you or a loved one has had a life threatening event due to Invokana call out Invokana Helpline today.
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.
Faulty Knee Replacement Lawyers
Depuy Knee Replacement, Zimmer Persona Knee
Zimmer NexGen Knee Replacement Lawyers
Zimmer NexGen “High-Flex” femoral components
Cruciate Retaining (Zimmer CR Flex)
Zimmer Legacy Posterior Stabilized (Zimmer LPS Flex)
Zimmer Gender Solutions High-Flex Knee
MIS Total Knee Procedure Stemmed Tibial Component Fixed Bearing Precoa
Signs Of Knee Implant Failure
early joint breakdown due to poor design or manufacturing,
loosening at the knee joint,
or wear and tear.
Failed Knee Replacement Complications
Limited range of movement
Warm, inflamed or red skin
Instability in the knee
Loosening of the knee implant
Swelling and/or pain in the knee
Abnormal sound in the knee implant
Decreased ability to walk
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,
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.
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