Jersey City

Physiomesh Hernia Mesh Lawyers

Ehicon Physiomesh Recall Lawyers

The Physiomesh is a Flexible Composite Hernia  Mesh  used in hernia repair surgery. The Physiomesh is made of a synthetic plastic-like material called polypropylene and is used as a patch to repair the hernia. It is the same exact material used in the Ethicon vaginal mesh that has caused problems in thousands of women.

Physiomesh Complications

 

  • Need for revision surgery due to mesh failure
  • Recurring hernia due to failure of the Physiomesh
  • Pain after surgery.
  • Recurring hernia in the first 6 months following surgery

Ethicon Physiomesh Lawyers Filing Physiomesh Lawsuits

If you have had a hernia repair surgery using the Ethicon Physiomesh and are experiencing complications contact our Physiomesh lawyers. Lawsuits are being filed against Ethicon Inc. for failure of their Physiomesh.

 

 

 

Bard IVC Filter Lawsuit Update | Cook IVC Filter Lawyer

The federal multi-district litigation panel for the Bard IVC Filters  has appointed a federal judge in Phoenix to oversee the C.R. Bard Inc. (NYSE: BCR) IVC filter consolidated lawsuits for all Bard Inferior Vena Cava filter lawsuits nationwide.

An  IVC filter was designed to capture  blood clots in patients who could not use  blood thinners. Our IVC Filter lawyers are filing defective IVC Filter lawsuits for people injured by a defective IVC Filter. Injuries include those from the fracturing of the filter and parts of the filter migrating and puncturing vital organs.  Faulty IVC filters puncture veins, fracture and migrate to other parts of the body causing injury and even death.

Why Are IVC Filter Lawsuits Being Filed?

IVC filter is problematic because   pieces can break off and thru-out the body and injure  parts of the body or get embedded in the organ tissue. These temporary IVC filters are supposed to be taken out within six months.  Very often the device is not removed in time to prevent complications.

IVC Filter Complications

Deep vein thrombosis
Difficulty in removing the filter
Movement of the entire filter or filter fragments to the heart or lungs
Fracture of the filter
Migration of the filter to another part of the body or vital organ
Perforation of the inferior vena cava
Tilting of the filter

If you or a loved one has been injured by a defective Bard or Cook Ivc Filter contact us to speak to an IVC Filter lawyer.

 

 

 

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.

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