Florida

Florida Lawyers File Stryker Rejuvinate, ABG II Modular Stems Hip Replacement Lawsuits

Stryker Hip Replacement Lawyers are filing lawsuits for seniors with a defective Stryker hip replacement. Local Hip replacement lawyers continue to file lawsuits for the Stryker Rejuvinate and ABG II Modular Stems Due To Complications.

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  •     Loosening or dislocation of the hip joint
  •     Corrosion and fretting at the modular-neck junction which may lead to adverse local tissue reactions
  •     Excessive metal debris leading to high levels of metal ions in the blood
  •     Inflammation of surrounding tissue
  •     Pseudotumors
  •     Swelling and pain at the implant site
  •     Difficulty  walking
  •     Need for additional painful revision surgeries
  •     Rehabilitation and decline in quality of life
  •     Metallosis
  •     Hypersensitivity/allergic response
  •     Swelling
  •     Unexplained hip pain more than three months post-surgery

Many seniors who underwent hip replacement surgery did this with the idea that their senior years would be better as a result. They could travel, play golf and be active. But, this has caused severe pain and suffering at a  time when retirement should mean pleasure. We must get justice and stand up against these companies. Florida Stryker lawyers of Free Legal Shield are here to help Florida seniors and loved ones; a parent or grandparent who  is suffering from one of these  Stryker hip replacements.

Call now. Get a Stryker Hip replacement lawyer.

Dialysis Injury Help Center, GranuFlo Naturalyte Helpline

Lawyers for GranuFlo and Naturalyte are filing lawsuits for dialysis injury from Granuflo and Naturalyte. Fresenius Medical Care’s dialysis product GranuFlo is  a medication  that  dialysis centers   use to treat acute and chronic kidney failure.
 

Your kidneys clean the blood of waste  products  and help maintain the body’s pH level. When they fail, the body’s pH level become more acidic than is should be.  Kidney failure is treated with chemicals that help the body convert ph level. These substances convert  into the alkaline substance bicarbonate, which neutralizes some of the acid buildup in the blood stream.
GranuFlo  and Naturalyte have had issues with this conversion and have shown instances of immediate  heart attacks as a side effect. GranuFlo contains more bicarbonate than other dialysates.

The June 2012 New York Times article describes Fresenius’s knowledge of these risks  of granuFlo and Naturalyte and the product’s high bicarbonate level. According to the article, Fresenius sent a memo to its clinics warning that the higher bicarbonate levels in GranuFlo had caused 941 heart attacks in the company’s own clinics in 2010, leading the company’s researchers to estimate that GranuFlo increases a patient’s risk of heart attack by six times. Fresenius did not send the memo to GranuFlo-using clinics that the company didn’t own, however, until March 29, 2012, when the FDA consequently began investigating Fresenius for possible violations of federal regulations, the Times reports.

Currently GranuFlo and Naturalyte lawyers are accepting claims against Fresenius for immediate hear attack  form their GranuFlo and Naturalyte products. A number of dialysis patients may have already been injured by GranuFlo. If  GranuFlo diaysis medication caused a sudden heart attack or cardiac arrest, hemodialysis cardiac arrest or cardiopulmonary arrest, stroke, or arrhythmia speak to a GranuFlo lawyer now by calling the GranuFlo legal team of free legal Shield. We seek justice for seniors.

Mesothelioma Lawsuits, Mesothelioma Lawyers, Asbestos, Lung Cancer

Mesothelioma is a fatal lung cancer caused by exposure to asbestos. Certain work environments are more prone to causing mesothelioma.

  •     Shipyard Workers
  •     Construction Workers
  •     Power Plant Workers
  •     Chemical Plant Workers
  •     Industrial Workers
  •     Insulators
  •     Boiler Workers
  •     Auto Mechanics

Types of mesothelioma

  •     Pleural mesotheliomas start in the chest.
  •     Peritoneal mesotheliomas begin in the abdomen.

 

 Symptoms of Mesothelioma

  •     Shortness of breath and
  •     A heavy feeling in the chest area.
  •     Pain under the rib cage.
  •     Pain or swelling in the abdomen.
  •     Lumps in the abdomen.
  •     Weight loss for no known reason.

Mesothelioma Comes from Inhaling Asbestos For Long Periods Of Time

When a person breathes in the small asbestos fibers, they remain in the lungs and cause scar tissue to form on the the tiny air sacs where oxygen and carbon dioxide are exchanged. The amount of oxygen that is available to the body is reduced through asbestos exposure and worsened through repeated inhalations for long periods of time.

Notable asbestos verdicts in the United States include:
Mississippi

– In May 2011, the current largest plaintiff's asbestos verdict was awarded to a former oil refinery worker. Union Carbine and Chevron Phillips Chemical were instructed to pay the man $322 million.
San Francisco, California

– Alfred Todak, a former Navy electrician, was awarded $22.7 million, and his was wife was awarded $11 for loss of consortium.
Madison County, Illinois

– Madison County's asbestos verdicts have typically favored the plaintiff, including the 2000 Hutchinson v. Shell Oil Company case in which a man was awarded a total of $34.1 million.

Incidence of Mesothelioma

State/Region  Incidence per 100,000
New Jersey  1.52
Seattle-Puget Sound  1.44
Louisiana  1.37
Connecticut  1.08
Greater California  1.06
Utah  1.02
New Mexico  0.99
Detroit  0.89
Kentucky  0.85
Iowa  0.80
Georgia  0.70

The six states with the highest mesothelioma death rates include: Maine, Wyoming, West Virginia, Pennsylvania, New Jersey and Washington

Mesothelioma Lawyers

If you or a loved one has been diagnosed with mesothelioma or asbestos related cancer call our mesothelioma helpline today. We will connect you with an experienced mesothelioma, mass tort lawyer. Mesothelioma lawsuits are mass torts and must be handled by an experienced mass tort lawyer.

  

 

 

Januvia, Byetta Risks of Pancreatic Cancer, Lawyers Looking At Lawsuits

New Information on Byetta and Januvia is gaining interest by lawyers for Pancreatic and Thyroid Cancer. Type II Diabetics are potential victims of cancer from these Diabetic drugs.

Popular diabetes drugs may raise pancreatic cancer risk, study suggests
By Steven Reinberg, HealthDay
Updated 9/23/2011 6:15 PM

People with type 2 diabetes taking the drugs Januvia or Byetta might have an increased risk of developing pancreatitis and pancreatic cancer, a preliminary study suggests.
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The study also found that Byetta (exenatide) may raise the risk of thyroid cancer.

Although the links aren't conclusive, they merit further investigation, the researchers noted.

"We have raised concern that there may be a link, but we haven't confirmed it," said lead researcher Dr. Peter Butler, director of the Larry L. Hillblom Islet Research Center at the University of California, Los Angeles. "We need to do more work to figure out whether this is real or not."

Both drugs help control blood sugar levels by encouraging production of a hormone called glucagon-like peptide 1 (GLP-1).

Januvia (sitagliptin) and Byetta, an injectable drug, are a new way of treating type 2 diabetes, and they potentially have advantages over older medications, Butler said. But, because these drugs are new, they're "the ones we know least about," he said. "When new drugs come out, the long-term side effects of these drugs are not well understood."

For the study, recently published in the journal Gastroenterology, Butler's team used 2004-2009 information in the U.S. Food and Drug Administration's database on adverse events, which are reported by doctors whose patients use these drugs.

When compared to other treatments, the researchers found a sixfold increase of reported cases of pancreatitis (inflammation of the pancreas) linked to patients taking Januvia or Byetta; a 2.9-fold increase in reported cases of pancreatic cancer among those taking Byetta and a 2.7-fold increase of reported pancreatic cancers among Januvia users.

In addition, they also noted an increase in reported cases of thyroid cancer with Byetta.

This latest study builds on earlier research, published in a 2009 issue of Diabetes, which found an increase in pancreatitis in rats whose GLP-1 levels were raised, the researchers said.

Butler is quick to point out that these increases in pancreatic cancer risk, while statistically significant, are not specifically related to patients, but rather to an increase in doctors reporting these cases to the FDA.

"It is important to avoid alarmism and have people stop medicines that they may be benefitting from when the risk is not yet defined," he stressed.

"If the drug and you are working well together, I wouldn't say there is any reason to stop the drug, based on the evidence we have right now," he said. "But if you have any concern you should talk to your doctor about it."

Being overweight is an important risk for both pancreatic cancer and type 2 diabetes, Butler noted. So the first advice to overweight patients with type 2 diabetes is to lose weight. "By doing that, you reduce the risk of pancreatic cancer," he said.

In addition, the first medication used to control blood sugar in type 2 diabetics is metformin, which by itself may reduce the risk for pancreatic cancer, Butler said. Metformin is an older drug with a well-known safety profile, he noted.

Dr. Mary Ann Banerji, director of the Diabetes Treatment Center at SUNY Health Science Center Brooklyn in New York City, said that "this is not perfect data."

However, Banerji does not prescribe these drugs for patients who have had a history of pancreatitis or a family history of thyroid cancer. There are alternatives such as metformin and insulin, as well as Avandia and Actos, she said, but studies have turned up an increased risk for heart attack and heart failure in the last two drugs. The FDA has removed Avandia from pharmacy shelves, and the agency issued a warning last summer that there is a possible increased risk of bladder cancer in patients who take Actos for more than a year.

The concerns about Januvia and Byetta "should not be blown out of proportion," Banerji said. "You prescribe them on an individual basis, because, in the end, all of medicine is individual," she said. "We should use these drugs judiciously along with metformin."

Industry representatives, insisting that no studies involving these drugs have found an increased risk of pancreatitis or pancreatic cancer, stand by their products. The database used for the study contains information on doctor-reported cases and does not reflect cause-and-effect, they said.

Dr. Barry Goldstein, vice president and therapeutic area head for diabetes and endocrinology at Merck Research Laboratories, which makes Januvia, said that "there has been no association shown between Januvia and pancreatitis."

"We have full confidence in Januvia, which is used by millions of patients around the world," he said.

Anne Erickson, a spokeswoman for Amylin Pharmaceuticals, makers of Byetta, said that "the conclusions of the study are in contrast to other nonclinical, clinical and adequately conducted post-marketing epidemiological studies."

Epidemiological studies have not established a significantly increased risk of pancreatitis associated with Byetta, she said. "To date, the available data do not demonstrate that exenatide increases the overall risk of cancer in humans."

Another expert, Dr. Ronald Goldberg, professor of medicine, biochemistry and molecular biology at the University of Miami Miller School of Medicine, said the findings merit consideration. "I don't think the study is definitive, but it raises a flag and is clearly something we need to pay attention to going forward."

There is "more benefit than risk with these drugs, based on our current knowledge," he

Fosamax Lawyers for Women Injured By Fosamax, Femur Fractures

Fosamax Femur Fracture Lawyers

Our Fosmax lawyers are filing lawsuits for Femur faracture from Fosmax.

Fosamax (alendronate) is a part of the class of bisphosphonates. Fosamax  alters the cycle of bone formation and breakdown in the body. Fosamax slows bone loss while increasing bone mass, which may prevent bone fractures.

Fosamax is used in men and women to treat or prevent osteoporosis that is caused by menopause or by taking steroids. Fosamax is also used to increase bone mass in men who have osteoporosis, and to treat Paget's disease of the bone in men and women.

However, Fosamax has been a central focus of lawsuits.  Fosamax has been linked to a number of severe side effects that has required many revisions of the Fosamax Warning label.  These side effects have brought about a wide range of Fosamax lawsuits. Fosamax has been shown to cause Osteonecrosis of the Jaw Injury, Femur Fractures, and Severe Musculoskeletal Pain.

FDA Issues Fosamax Warning

On Oct. 13, 2010, the U.S. Food and Drug Administration issued a Fosamax safety about the risk of atypical femur fractures. The victims of Fosamax are mostly  post menapausal women who lose bo have osteoporosis due to loss of estrogen.  Fosamax has caused what it was prescibed to help, femur fractures.

Reports from the Hospital for Special Surgery and Columbia University Medical Center have reported  that Fosamax changes bone remodeling in an unknown manner and may contribute to Fosamax Femur Fractures.  Many medical journals have reported Femur faractures from Fosamax. According to the geriatric social worker who runs the helpline" Our concern is with the elderly who have been prescibed Fosamax. Femur fractures heal slower as we age and usually require long periods of rehabilitation and physical therapy."

The femur is one of the largest, and strongest bones in the body. The femur is the thigh bone. The femur extends from the hip joint down to the knee joint. Because the femur is such a strong bone, it can take tremendous force to cause a femur fracture. Spontaneous femur bone fractures are extremely unusual and  serious for anyone but, especially serious for older women."

For the most part Femur fractures are caused by extremely high impact accidents like car accidents or   Falls from a height although they can happen to the fragile elderly from a fall.

It is interesting to note  that womwn may also have bone that is weakened by osteoporosis thae exact medical condition Fosamax was to help.

Femur fractures include:

  •         Hip Fractures
  •         Femoral Neck Fractures
  •         Intertrochanteric Femur Fractures

Femur fractures almost always require surgery and long periods of rehabilitation and Physical therapy. Sometimes they result in a length variatopn due the a potential hip rotation during surgery and cam lead to poor balance. In some cases the pre- fracture level of functioning does not return completely.

Fosamax MDL Update

All Fosamax lawsuits alleging that  the victim  sustained an atypical femur fracture as a result of taking the bisphosphonate Fosamax, can also include victims who took similar medications such as Reclast or Boniva as long as they did, in fact, take Fosamax.

If you a family member or someone you are a caregiver for has a spontaneous femur fracture and is on one of these medications contact our Fosamax Helpline to find out if you can be included in the current Fosamax litigation underway.

Current Fosamax News

 A U.S. District Court judge has  ordered  hundreds of  Fosamax lawsuits returned to the state courts and out of the MDL.Judge John Keenan ordered that 200 Fosamax  cases a month be returned to the state  courts where they were filed.

 

Florida Unpaid Time and Half Claims, Unpaid Overtime Lawyers

If you have not been paid time and a half in Florida for overtime worked you may have a wage and hour claim against your employer.  You deserve to get paid according to Florida law for the hours you put in. You may have a class action lawsuit for unpaid wages. Our lawyers for unpaid wages offer legal help for:

  •     Lawyers for time and a half pay for overtime,
  •     Lawyers for Fair Labor Standards Act,
  •     Labor Emplyment Lawyers ,
  •     Class actions  for Unpaid Overtime Wages,
  •     Lawyers for Wage and Hour Claims,
  •     Lawyers for FLSA and Unpaid Commissions,

Overtime pay of time and a half is due once an employee has worked forty (40) hours in a work week.

 The Fair Labor Standards Act (“FLSA”)  

The FLSA establishes the rules for  governing employees’ rights to minimum wage and overtime pay which include:

  • Time and a half wages for employees for all hours over 40 worked in a workweek.
  •  A minimum wage of at least $7.25 for all hours worked.

What can I expect if I win a wage and hour claim against my employer?

  • Back pay for all unpaid overtime, beginning two (2) years before the lawsuit is filed.
  • Double the amount of unpaid wages, in some instances
  • Your employer will be liable for the attorneys fees

 

For the full details about your Florida unpaid wages, to file an unpaid wages claim and to see if you have a claim for unpaid overtime call our wage and hour claim hotline today

In Florida you deserve to get paid your full WAGES FOR HOURS WORKED and all overtime back pay for unpaid wages claims.

Meningitus Outbreak Due To Steroid Medication, Meningitus Lawyers Ready as 26 States Effected

A menigitus outbreak is now expanding to 26 states. The outbreak is linked to a contaminated shipment of steroid medication from a Massachusetts compounding pharmacy. Product liability lawyers are looking at injuries and potential deaths increasing. According to the product liabilities lawyers of Free Legal Shield there may be a huge number of pharmaceutical liability lawsuits filed against the manufacturer of thi s product. A manufacturer can be held liable for injury and death due to contamination of it's products. The hardest hit has been a clinic in Nashville Tennessee.


By

Michelle Castillo /
CBS News/ October 4, 2012, 3:22 PM
Meningitis outbreak may affect more than 23 states

The Centers for Disease and Control and Prevention (CDC) and Food and Drug Administration (FDA) announced today they are advising medical professionals not to use any products manufactured by the New England Compounding Center in Framingham, Mass., due to an outbreak of fungal meningitis tied to some medications made by the company.

Three lots of the company's preservative-free methylprednisolone acetate that go back to July 2012 have been recalled and are believed to be the cause of the recent outbreak. Thirty-five cases of fungal meningtitis in six states have been identified, with five deaths. The majority of the cases, 25 in total, have been discovered in Tennessee.

"Given the severity of illness, we believe these precautionary measures are warranted to protect public health," Ilisa Bernstein, director of the FDA office of compliance, said to reporters during a conference call today.

    Meningitis outbreak sickens 35 in 6 states, kills 5
    Tenn. meningitis outbreak tied to steroid shots

Dr. Benjamin Park, medical epidemiologist with the Centers for Disease Control and Prevention, told reporters that 23 states may have received shipments of the tainted product. These states include: California, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Maryland, Michigan, Minnesota, North Carolina, New Hampshire, New Jersey, Nevada, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Virginia, Texas and West Virginia. A total of 75 facilities may have received product from one of these three recalled lots.


Deadly meningitis outbreak in U.S.

However, because the New England Compounding Center is licensed in all 50 states, there is a possibility contaminated products may be in other areas, Bernstein said.

"We don't know the scope of this," she admitted.

The initial three-lot recall by the New England Compounding Center involved 17,676 vials, the CBS News Investigative Team reported. There were two complaints filed against the company — one in 2002, one in 2003 — that were investigated and as a result the company entered into an agreement in 2006 with the Massachusetts Department of Health to correct any deficiencies. That same year, the FDA warned the company against compounding topical anesthetic creams for general distribution.

In March 2012, a complaint unrelated to the meningitis case was filed against the company regarding the potency of its eye medication. That complaint is still open and pending, according to the investigative team.

Play Video
Meningitis outbreak linked to Mass. pharmacy

Fungal meningitis is a non-contagious form of the disease. It is often caused by fungus normally found in leaf mold. Authorities said some people were experiencing mild stroke-like symptoms, including slurred speech, and difficulty walking and urinating. Other fungal meningitis symptoms include worsening and severe headache, nausea, dizziness and fever.

It can be treated with high-dose antifungal medications, usually given intravenously in a hospital. The earlier the disease is diagnosed and treated, the better the chances of survival are.

"We think that early antifungal treatment can improve the outcome of these patients," Park said.

Park said that the CDC was notified of a patient with an onset of meningitis 19 days after receiving an epidural steroid injection on Sept. 21 in Tennessee. Although all initial cultures were negative, fungus was isolated from the patient's cerebral spinal fluid. On Sep. 28, the CDC was notified of cases outside of Tennessee.

In total, one case in North Carolina, two cases in Florida, four cases in Virginia, two cases in Maryland and one case in Indiana have been discovered in addition to the 25 cases in Tennessee. Three people have died in Tennessee, as well as one person from Virginia and one person from Maryland.

The victims tend to be elderly because of the nature of patients who receive spinal epidural injections because of lower back pain. Overall, many of the patients were somewhat healthy until infection.

Play Video
Woman may have been exposed to meningitis

On Oct. 1, the New England Compounding Center voluntarily shut down their manufacturing center. During a FDA investigation of the plant, the investigators discovered contaminants in an unopened vial.

"Materials from an unopened vials was looked at under the microscope at an FDA lab and what was looked at under the microscope looked like a fungal matter," an FDA spokesperson confirmed.

The FDA added that they are working with the firm to get more information about their products. The

GranuFlo Lawyers, NaturaLyte Lawsuits

 

Fresenius Medical is the manufacturer of  GranuFlo and NaturaLyte acid concentrate. These are drugs used in  dialysis treatment. There has been a recall of these dialysis drugs and  lawsuits are being filed.

Injury and death has resulted from these drugs:

  •  GranuFlo cardiovascular death,
  •  GranuFlo sudden cardiac death,
  •  GranuFlo cardiopulmonary arrest,
  •  GranuFlo heart attack,
  •  GranuFlo catastrophic cardiovascular injuries

 

Fresenius manufactures GranuFlo and NaturaLyte used in dialysis. These drugs cause alkalosis, a condition associated with an increase in cardiovascular fatalities.

 

The FDA received complaints describing alkali dosing errors that occurred during hemodialysis using dialysate concentrates containing acetic acid and acetate. When metabolized, these potential sources of alkali can contribute to elevated bicarbonate levels in patients undergoing hemodialysis.

 

This can contribute to metabolic alkalosis, which is a significant risk factor associated with :

 

Low blood pressure

Cardiopulmonary arrest

Cardiac arrhythmia

Sudden heart attack

Stroke

Hemodialysis cardiopulmonary arrest

 

A study which was conducted between January and December of 2010 found that patients with pre-dialysis bicarbonate levels greater than 28mEq/L were 4.7 times more likely to suffer a cardiac arrest. The study also discovered that patients with pre-dialysis potassium lower than 4 mEq/L had a 6.3 times higher risk of cardiac arrest.

 

In May 2012 the FDA notified health care providers to consider the presence and quantity of acetate, citrate, and/or acetic acid in dialysate concentrates when determining the patients’ dialysate prescription.

There is a GranuFlo and NaturaLyte Class 1 Recall

 

Serial numbers for recalled Naturalyte Liquid Acid Concentrate range from:

 

08-0231-4, 08-1001-0, 08-1201-8, 08-1231-3, 08-1251-1, 08-1301-4, 08-2201-5, 08-2231-2, 08-2251-0, 08-2301-3,08-2351-8, 08-3201-4, 08-3231-1, 08-3251-9, 08-3301-2, 08-4123-1, 08-4223-7, 08-4225-1, 08-4230- 2, 08-4231-0, 08-4323-5, 08-4325-1, 13-1251-1, 13-2201-5, 13-2231-2, 13-2251-0, 13-3231-1, 13-3251-9, 13-4123-1, 13-4220-1, 13-4225-1, 13-4325-

 

Serial numbers for recalled Naturalyte GranuFlo (powder) Acid Concentrate range from:

 

OFD1201-3B, OFD1251-3B, OFD2123-3B, OFD2201-38, OFD2220-3B, OFD2223-3B, OFD2225-3B, OFD2231-3 B, OFD2251-3B, OFD2301-3B, OFD2323-3 B, OFD2325-3B, OFD3201-3B, OFD3231-3B, OFD3251-3B, OFD3301-3B

GranuFlo & NaturaLyte is one of the most widely prescribed dry acid products used for dialysis  at Fresenius'  clinics, as well as other hemodialysis centers that purchase their dialysis supplies from Fresenius.  It is estimated that 125,000 patients in non-Fresenius clinics are treated with GranuFlo.

Dilaysis Patient Alert

If you, a loved one or someone you care for has been injured by these products contact us for a GranuFlo and NaturaLyte lawsuit.

Bladder Sling Lawyers, Vaginal Mesh Lawsuits

The bladder mesh is a vaginal mesh product primarily used for urinary incontinence. This mesh sling has caused severe complications and bladder mesh lawyers are filing lawsuits. Many women with a bladder mesh do not realize they are eligible to file a vaginal mesh lawsuit.

What is a Bladder Sling?

Urethral sling or bladder sling  is used  to treat urinary incontinence by placing a sling around the urethra to lift it back into a normal position and to exert pressure on the urethra to aid urine retention. The sling is attached to the abdominal wall. A bladder sling is a mesh device and is part of the vaginal mesh litigation. The complications of a failed bladder sling is increased incontinence or trouble voiding. Many women have needed to self catherize.

 Bladder Sling Complications?

According to the July 2011 FDA news release, the most common complications associated with surgical mesh bladder slings is erosion thru the vaginal wall or into the bladder, pain during sexual intercourse, bleeding, infection, perforation of various pelvic organs (bladder, colon, vaginal walls), and urinary incontinence or problems voiding as well as; neuromuscular problems, emotional problems, mesh contraction/shrinkage, and even a reoccurrence of POP and/or SUI.

Bladder sling lawsuits are being filed on a contingency fee basis against the mnaufacturers of the bladder sling:

        Bard Avaulta Support System
        AMS Elevate Prolapse Repair System
        AMS Apogee Vault Suspension System
        AMS Perigee System
        AMS Monarc Sling System
        AMS Sparc Sling System
        Ethicon Gynecare Gynemesh
        Ethicon Gynecare Prolene Soft Mesh
        Ethicon Gynecare Prolift Pelvic Floor Repair System
        Ethicon Gynecare TVT Transvaginal Sling
        Boston Scientific Pinnacle Pelvic Floor Repair Kit
        Boston Scientific Uphold Vaginal Support System
        UGYTEX Dual Knit Mesh
        Coviden IVS Tunneler Sling

Contact us today.

Stryker Hip Replacement Lawyers, Stryker Hip Replacement Helpline

Adding to the Zimmer and DePuy metal on metal hip replacement Stryker has recalled it's latest metal component hip replacement implant.  Stryker has voluntarily recalled the  Rejuvenate metal component hip replacement implant and ABG II modular- neck stems
Stryker has voluntarily  stopped  market distribution of these hip replacements due to  increased risk of injury. The hip replacement implants have been shown to fret or corrode, harming body tissue and causing pain and  swelling. Other injuries include:

  •     Severe inflammatory reactions
  •     Pain in the groin
  •     metal toxicity ort poisoning
  •     high metal levels in the blood
  •     need for additional surgery
  •     Breakdown of muscles, tendons and other soft tissues in and around the hip joint
  •     Loss of surrounding bone
  •     Loss of mobility

While other types of hip implants such as those made by Johnson & Johnson and DePuy Orthopaedics Inc. involve a metal ball rubbing against a metal socket, the Stryker Rejuvenate products involve a metal neck inside a metal stem. The Stryker Hip replacement Helpline and  hip replacement lawyers are reaching out to all victims of the failed device for a potential multi district litigation.

The products have metal components and although they are not metal on metal run the same risks of chromium and cobalt toxicity poisoning. If you have been injured you are advised to contact your doctor immediately and contact the Stryker Hip Replacement Helpline for a Stryker lawyer