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Al Masaood & Associates

Al Masaood & Associates is one of the biggest and promising law firms established in September 2004 in the Emirate of Abu Dhabi providing advocacy and consultancy to the local and international clients.

The firm is comprised of talented and promising and diversified lawyers and legal consultants committed to deal with the client’s legal affairs in an effective professional manner. The firm demonstrates the sound handling of client matters and is committed to providing high quality, time and cost effective services to match the expectation of the client. The firm has extensive experience in the legal system of the Gulf Region, Middle East, Europe, Indo-Pak subcontinent, and the Southern Africa.

The lawyers of our firm negotiate and draft documents in Arabic, English, Hindi and Urdu.

It is a matter of satisfaction for me that Al Masaood & Associates have a professional and talented team of lawyers. Due to enormous volume of commercial transactions and the complex legal issues in the United Arab Emirates market our lawyers assist the local and international clients in an effective and professional manner.

Being lawyers, we always give priority to our clients and keep the emphasis on ensuring detailed attention to their needs in accordance with the social and economic environment in which they live.

We have been recognized as a professional and dedicated law firm providing a high quality services to our clients. We accomplish tasks by providing high quality and effective representation applying a personalized and professional approach.

Ibrahim Miller
Managing Director

Several Lawsuits Claim Ethicon Physiomesh Caused Injuries

Several Lawsuits Claim Ethicon Physiomesh Caused Injuries

Ethicon is a medical company that manufactures a medical device product called the Physiomesh Composite Mesh hernia patch. It is used for minimally invasive hernia repair procedures and other facial conditions that require a bridging or reinforcing material.

Ethicon Physiomesh Flexible Composite Mesh is an implanted medical device that can be used in laparoscopic operations to repair ventral hernias and other fascial issues requiring a reinforcing or bridging material. To get more information about the Ethicon Physiomesh you can navigate here.

Physiomesh patches are used for laparoscopic ventral hernia repair. The patches have a thick coating on both sides designed to prevent the mesh from sticking to bowels and tissues, as the mesh contains polypropylene, which can cause severe injuries if it attaches to other body parts. There are several lawsuits that file case and help the people who are victims of this, to know about this you can click here.

Ethicon Physiomesh has been used in hernia repair surgeries in the United States since 2010. Patients agreed to have the device implanted because they trusted Johnson & Johnson had tested the product for defects. In fact, Ethicon hernia mesh was never tested on humans. More than five years after the product was released in the U.S., Ethicon withdrew Physiomesh because of external reports showing high failure rates.

The likelihood of Physiomesh tearing apart inside patients and migrating within the body is increased because it contains less polypropylene than other mesh products.

Physiomesh Lawsuits

Unfortunately, the recall came too late for those who already had surgery with this product. Patients affected by defective Physiomesh experienced severe injuries, including:

Infections

Intestinal blockage

Chronic pain

Mesh migration to other areas of the body

Several patients have filed lawsuits against Ethicon alleging the Physiomesh hernia patch caused severe health problems and required corrective surgery. You can know more about the ethicon physiomesh lawsuit by surfing through the net.

ethicon-hernia-lawsuit.jpg (696×482)

Various parties can be held liable for injuries caused by an Ethicon Physiomesh product. For instance, lawsuits have been filed against the manufacturers of such products, usually under a product liability claim. This is based on the fact that the Physiomesh products may be considered defective.

Other parties can be held liable for prescribing or selling Physiomesh products despite the fact that they have been subject to a recall. These include doctors, pharmacists, and other persons who are in charge of recommending these types of products. Also, hospital institutions can be held liable for continuing to stock or distribute Physiomesh products.

Facts behind IVC Filter Lawsuits

IVC filters prevent blood clots from traveling to the lungs, heart, and brain in patients who cannot take blood-thinning drugs.

These small, cage-like devices are inserted into the vena cava, the body’s largest vein, which carries blood from the lower body to the heart.

IVC filters lawsuit can be either permanent or temporary in some cases; temporary filters are left in patients for far too long, causing serious problems and injuries.

Our IVC Filter Attorneys:

Partner with top litigation firms to provide outstanding representation.

Have handled 10,000+ cases and recovered millions of dollars.

Are backed by 50 years of collective legal experience.

Remain available 24 hours a day, 7 days a week and offer free case evaluations.

Treat clients with respect, traveling to them whenever necessary.

Charge no fees unless we recover a settlement / verdict on your behalf.If you want to know more about the IVC filter lawsuit, you may click here.

Call (888) 444-9136 today to schedule a free consultation with Pintas & Mullins. We are ready to advocate for you.

Dangers of IVC Filters

There are two IVC filter types: permanent and temporary, or retrievable.

Retrievable filters are designed for short-term protection, to be removed once the risk of blood clots resolves, yet are associated with higher rates of complications.

The longer an IVC filter is inside a patient, the more likely he or she is to suffer debilitating side effects.

Since 2005, the FDA has received more than 1,000 reports of IVC filter problems. These devices have alarmingly high fracture rates, which can cause organ perforation and other life-threatening complications.

Parts of the IVC filter may break off inside the body causing fragments to migrate to the heart, lungs or other nearby organs.

A fractured IVC filter may cause problems including:

  • Lower limb deep vein thrombosis (DVT)
  • Filter migration, fracture or embolization
  • Vein perforation, closing or blocking

  • Fluid buildup around the heart
  • Infection
  • Internal bleeding
  • Difficulty removing the device
  • Sudden death

IVC Filter Complications & Lawsuits

IVC filters capture blood clots, preventing them from reaching the lungs. The filter is a small, cage-like metal device shaped like a cone. The filter is implanted in the IVC just below the kidneys. The IVC filter allows the blood to flow regularly through the filter trapping the blood clot. Naturally-occurring blood thinners, or anticoagulants, helps in collapsing the clot.  To know more about bard ivc filter lawyer, you can browse the web.

IVC filters are generally implanted in people that experience pulmonary embolisms or deep vein thrombosis despite the regular and monitored use of prescribed anticoagulants. You can navigate here to know more about IVC filter complications & lawsuits.

  • IVC Filter Complications and Safety Concerns
    Initially intended to be permanent implants, the Food and Drug Administration began recommending in 2010 that IVC filters be removed as soon as the risk for pulmonary embolism has based and the patient can withstand the removal surgery. From 2005 to 2010, the FDA received nearly a thousand complaints regarding several serious and less severe issues related to IVC filters.

  • Long-term Use of IVC Filters Risks Damaging Patients
    IVC filters have led to several serious issues in patients. Filters left in the vein have broken into pieces or migrated wholly from their original position. This has led to perforating other organs creating serious damage and risk for patients.
    The heart is at significant risk from moving filters, leading to heart damage and fluid buildup, known as cardiac tamponade.
    Long-term use of IVC filters can also lead to recurrent pulmonary embolism, recurrent deep vein thrombosis (DVT), and thrombosis in the vena cava.
  • FDA Warning on Risks Associated with Long-term IVC Filters
    Originally approved by the FDA in 1979, the use of IVC filters has grown exponentially in the proceeding 30 years. However, based on the significant number of consumer complaints received by 2010, the FDA they recommended IVC filters be removed from patients when and as soon as possible.

Other Medical Problems
The FDA has also found less serious side effects of IVC filters, including irregular heartbeat, chest pains, and loss of breath which has led to loss of consciousness.

IVC Filter Lawsuits
Many individual and class-action lawsuits have been brought against manufacturers of IVC filters. At least one major manufacturer, Cook Medical Inc., has a pending multi-district litigation. The U.S. District Court for the Southern District of Indiana is overseeing the multidistrict litigation No. 2570.

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