Sheff Law – Experts in Trucking Accidents

September 20th, 2011

The holiday season is right around the corner.  Soon Massachusetts highways will be full of trucks and tractor trailers bringing products across the Commonwealth.

At Sheff Law, we have a long tradition of protecting people who are injured in trucking accidents.  These large freight trucks often make wide right-turns causing dangers to drivers.  We are also experts at wheel off cases in Massachusetts.

We recently secured a settlement of $5,000,000.00 for a family of a woman who was brain injured when a wheel fell off a truck and struck her car.

If you or a loved one has been injured by a trucking accident give an attorney at Sheff Law a call today.  Stay safe this fall on Massachusetts highways.

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Ground Turkey recalls linked to Salmonella

September 14th, 2011

Cargill Inc. has recalled an additional 185,000 pounds of ground turkey from its Arkansas plant after already recalling 36 million pounds of meat last month that had been linked to a salmonella outbreak.

To learn more about this recall and products liability visit Shefflaw.com.

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Number of Vaginal Mesh Patch Lawsuits Continues to Rise

September 9th, 2011

Lawyers across Massachusetts and the country are filing suits to protect the rights of injured women who received transvaginal mesh patches. It has been recently discovered that the U.S. Food and Drug Administration (FDA) used an abbreviated process known as 510(k) to clear use of Johnson & Johnson surgical mesh, this had lead to troubling consequences.   On July 13, the FDA warned of the rise in injuries related to the mesh, and has said that the device should be reclassified from moderate risk to high risk.

These transvaginal mesh patches have been known to break down after being inserted inside a woman’s vaginal wall.  This decomposition has lead to pain, discomfort, and even death. If you or someone you love has been injured as a result of transvaginal mesh patches you need a Boston lawyer suited to take on these massive medical device manufacturers.

The mesh started being used by surgeons in the 1950’s to repair abdominal hernias. In 1996, it was cleared for stress urinary incontinence by the FDA. In 2002, it was cleared for pelvic organ prolapse.  Manufactures of these mesh patches continue to disagree that they should be reclassified from moderate risk to high risk. Mesh makers include Johnson & Johnson, Bard, Boston Scientific of Natick, Massachusetts, and American Medical Systems. These makers believe that the mesh is safe and effective and that any serious adverse events remain rare and it is a valuable treatment option for women.

If you or a loved one have had transvaginal mesh implanted and have suffered pain, discomfort, malfunction or death, please contact Sheff Law immediately at (888) 423-4477 or by filling out our free consultation form.

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CELEXA LINKED TO ABNORMAL HEART RHYTHMS

August 24th, 2011

Celexa (citalopram hydrobromide) is a widely distributed and popular antidepressant. The Food and Drug Administration has notified healthcare professionals that when used at doses greater than 40 mg per day, Celexa can cause abnormal changes in the electrical activity of the heart. These changes can lead to an abnormal heart rhythm which can be fatal. Patients at the greatest risk are those with underlying heart conditions and those who are predisposed to low levels of potassium.

At personalinjuryattorney.com, we work with products liability attorneys across the United States who have experience representing people who have been hurt by harmful drugs. Celexa might be linked to the death of patients. If you or a loved has taken Celexa and now has abnormal heart activity contact a products liability lawyer today by filling out a free evaluation. We’ll help you get the compensation you deserve.

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Volvo Recalls Vehicles with Steering Problems

August 1st, 2011

Volvo has announced the recall of over 8,000 S80 models because of power steering fluid problems. Volvo Cars has said that the issue could result in a burst hose at the steering gear. They said it can also cause a sudden loss of power steering, increasing the chance of an accident.

Officials say they have not received any reports of accidents or injuries due to this defect, but if you or a loved one has experienced any of the issues above and have been injured as a result, contact a product liability attorney today FOR FREE.

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Ford Recalling 1 Million Trucks

July 28th, 2011

Ford motor Company has recently issued the recall of 1 million trucks due to problems with the fuel tank strap. The straps may corrode resulting in the falling of the fuel tank.

There has already been 3 fires and one injury caused by this defect.

If someone you know or love has been injured as a result of a products liability injury, or a Ford Truck recall, you need an attorney with the experience, credentials, and resources to stand up to the companies who hurt you. Contact an attorney FOR FREE.  An attorney will personally review the information you provide and may contact you to discuss your legal options.

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FDA Alert: Diflucan Use May Be Associated With Birth Defects

July 25th, 2011

The FDA has announced and is informing the public that the use of Diflucan (fluconazole) over the course of a long period of time and in high dosages during the first trimester of pregnancy may be associated with rare, but distinct birth defects in infants.

If you or a loved one has taken Diflucan in high dosages for a long period of time while pregnant, you should contact your healthcare professional.

If you or someone you love has been injured as a result of harmful pharmaceutical drugs, you need an attorney with the experience, credentials, and resources to stand up to the people who hurt you. Contact an attorney FOR FREE. An attorney will personally review the information you provide and may contact you to discuss your legal options.

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FDA Discovers a Potential Risk of Oral Osteoporosis Drugs causing Esophageal Cancer

July 22nd, 2011
The FDA has recently informed healthcare professionals and patients about their evaluation of data from published studies revealing that the use of oral bisphosphonate drugs may lead to an increased risk of cancer of the esophagus. Oral bisphosphonates are generally used to prevent and treat osteoporosis as well as to treat other bone diseases such as Paget’s disease.
The oral osteoporosis drugs that are included in the FDA’s evaluation include Fosamax (alendronate), Actonel (risedronate), Boniva (ibandronate), Atelvia (risedronate delayed release), Didronel (etidronate), and Skelid (tiludronate).
There has been contrasting findings from the studies which assess the risk of esophageal cancer from these drugs.  The patients who did not follow the specific directions for the use of oral bisphosphonates have been reported to have Esophagitis or other esophageal related side effects.  Patients are urged to discuss with their doctor the pros and cons of taking oral bisphosphonates and how long they will be expected to take them.  If a patient develops swallowing difficulties, chest pain, new or worsening heartburn, or they have trouble or pain when swallowing it is imperative that they contact a healthcare professional immediately.

The FDA has yet to make any final conclusions as to whether taking an oral bisphosphonate drug increases the risk of esophageal cancer. However, if you or a loved one has or is suffering from esophageal cancer, you should contact a Fosamax Cancer attorney immediately to preserve your legal rights.

You should continue to monitor this developing situation. The FDA will continue to evaluate all available data supporting the safety and effectiveness of bisphosphonate drugs and will continue to provide updates.

If you or a loved one has taken a osteoporosis drug, including Fosamax, and now has been diagnosed with esophageal cancer, contact a Fosamax Cancer Lawyer lawyer immediately at (888) 423-4477  or by filling out a FREE EVALUATION.

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FDA Warning and Recall: Transvaginal Mesh Patch

July 14th, 2011

Contact a Transvaginal mesh patch lawyer

Childbirth can create many complications for the mother.  Two common conditions after childbirth are Pelvic Organ Prolapse and Stress Urinary Incontinence.  Both of these conditions create various complications and symptoms for the mothers.  Many products have been introduced by major companies to solve these conditions. One solution has been the creation of the transvaginal mesh patches or slings.  However, it has been widely published by the New England Journal of Medicine and now the FDA that these products could be defective leading to many serious complications for patients, including death.

Please find more information below regarding defective transvaginal mesh patches or slings, and the FDA warning associated with their use and how you can contact a transvaginal mesh patch attorney.

Transvaginal Mesh Patches/Slings and How They Work

When a woman has a child, there is commonly tissue damage, tearing, and other complications inflicted on the abdominal area as a result of labor and delivery.  When the tissue damage is left untreated, it can continue to increase the pressure on the bladder and the pressure on the abdominal organs.  These are often signs of Pelvic Organ Prolapse and/or Stress Urinary Incontinence. If you or a loved one has experienced complications from transvaginal mesh patch, contact a defective transvaginal mesh patch lawyer today.

As stated above, several companies have released transvaginal mesh products onto the marketplace, and some of these companies include:
•    American Medical Systems
•    Bard
•    Boston Scientific
•    Ethicon division of Johnson & Johnson
•    Gynecare division of Johnson & Johnson
•    Johnson & Johnson

If you or a loved one has been a victim of a product made by one of the companies above, you need a transvaginal mesh patch lawyer to represent you and your interests.

Serious Injuries Reported
Defective Transvaginal Mesh patches have caused or led to perforation or puncture of the bladder, intestines and bowels, as well as blood vessels in and around the vaginal wall. The Food and Drug Administration (FDA) reported over 1,000 incidents of potentially fatal complications associated with transvaginal mesh patches.

What Does The Patch Do?
The transvaginal mesh patch is inserted by a doctor and stretched across the vaginal wall, the patch help support  internal organs that were once supported by the vaginal wall until a significant stretching, such as during childbirth, may have damaged the tissue.

Dangerous Symptoms and Side Effects of Transvaginal Patches Include:
•    Severe bleeding
•    Erosion of the vaginal epithelium
•    Serious infection
•    Return of Pelvic Organ Prolapse (POP)
•    Urinary incontinence

Recent Research Indicates Patches’ Serious Risks
The New England Journal of Medicine in May, revealed negative side effects associated with the transvaginal mesh patch. The study measured the effectiveness of the patch compared to that of colporrhaphy, the traditional treatment of sticking connective tissue in the vaginal wall back together.

What You Should Do:
First, if suffering severe complications, contact your doctor at once and seek medical attention.

If you are experiencing complications, contact the medical provider or doctor who inserted the patch and ask which manufacturer you have been given and schedule an appointment to see your physician as soon as possible.

Second, if you or a loved one has suffered an injury as a result of the transvaginal mesh patch, please contact a Transvaginal mesh patch lawyer immediately at (888) 423-4477 or by filling out a FREE EVALUATION .

Contact us today, there is no obligation.

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Mazda Recalls 103,300 Vehicles

July 5th, 2011

The Mazda Motor Coporation has announced a recall of 103,300 cars that were made in 2008 and 2009 due to problems with motors and windshield wipers.  The motor in the 2008-2009 Mazda 3 and the Mazda speed 3 vehicles have a problem in a ground terminal for the wiper motor that “may have been inadvertently bent during assembly.” (Mazda)   The problem with the windshield wipers is that during severe weather conditions they come off which could be very dangerous. The recall involves Mazda vehicles made between January 7th 2008 and November 28th, 2008.  The National Highway Administration reported that the recall will take place on or before July 15th, 2011.

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