IVC Filter Lawsuit

FDA Warns Against the Use of IVC Filters

Due to Migration, Perforation, and


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Bard Inferior Vena Cava Filters Cause Serious Complications

Patients who suffer from the threat of pulmonary embolism (or blood clots) and are contraindicated for anticoagulation therapy may find themselves at the mercy of a new and vastly unproven device known as an Inferior Vena Cava filter or IVC. This device which roughly resembles a bird’s nest is inserted into a patient’s arteries to prevent clotting. IVC filters, especially the Bard G2® and Recovery®  models gained wide use since the 2003 introduction, and now patients many are now at risk. This device was supposed to reduce or eliminate the risk of pulmonary embolism, a serious clotting condition that often results in death.

Accordingly, IVC filter placement has more than doubled over the last decade and that while uncomplicated filter placement is a relatively straightforward ambulatory procedure, the setting up of inferior vena cava filter registries and reporting outcomes are not mandatory. Since the first IVC filter was granted premarket approval FDA has received roughly one thousand adverse reports involving these filters in its MAUDE database which is maintained by the FDA as a voluntary reporting system. The overwhelming complaint was that IVC Filters, especially those designed and manufactured by Bard, break down and embolize throughout the body.

Bard G2 and Recovery IVC Filters Fail’You May Be Entitled To Compensation Comprehensive research of IVC filers produced by Bard, Crux , Cook Medical, Greenfield, Gunther Tulip and Boston Scientific over the last seven years coupled with the reports made by physicians and consumers, has prompted the FDA to urge physicians recommending an IVC filter to think twice . The FDA has told physicians to consider the risk and benefits for individual patients instead of simply choosing the IVC for all patients who are ineligible for anticoagulation therapy, and to remove the device once the symptoms have diminished.

The dangers and side effects caused by IVC Filters, especially those manufactured by Bard, will likely result in lawsuits.

These lawsuits will stem from the IVC device:

  • Migrating from its initial implantation location
    Embolizing, or breaking and entering the blood stream of the patient
    Perforating the patient’s veins
    Fracturing and traveling throughout the bloodstream

These defects are often not manifested by any symptoms in patients which makes identification of the problem very difficult. Experienced National IVC Filter Counsel to Protect Your Right to Compensation If you have an IVC Filter, whether manufactured by Bard, Boston Scientific, Cook Medical or Crux, please contact us and we will direct you to someone that handles defective and recalled medical device lawsuits across the country.

This website is sponsored as an informational service to those individuals that have had IVC filters implanted and experienced migration, fractures, embolization, or perforation.

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Bard IVC Filter Lawsuits

Our Bard IVC Filter lawsuit attorneys are currently reviewing cases for patients who were harmed by Bard IVC Filter complications such as migration and fracture. Bard IVC Filter problems can lead to potentially life-threatening injuries and a number of people who have suffered as a result of dangerous Bard IVC Filters have opted to file IVC Filter lawsuits for compensation.

If you or someone you love has suffered injury as a result of a Bard IVC Filter, our lnferior Vena Cava Filter lawsuit attorneys can help protect your legal rights. Bard IVC Filter Problems

Bard IVC Filters such as the Bard G2 IVC Filter and the Bard Recovery IVC Filter models are implanted in patients who cannot take anticoagulant drugs to prevent a pulmonary embolism or blood clot in the lungs. The filters are cone-shaped with legs that extend to intercept blood clots. In a study published in the Archives of Internal Medicine in 2010, researchers found the complication rate in Bard G2 IVC Filters to be up to 12%. In addition to these findings, the researchers also found that the rate of complication with Bard G2 IVC Filters grows in relation to the length of time the filter is allowed to stay in place, leading them to believe that the risk of complication can increase with the passage of time. Out of 80 IVC Filter patients studied, 13 patients were found to have at least one IVC fracture. This can lead to pieces of the filter entering the bloodstream and landing in the lungs, liver, and heart.

The risk of IVC Filter fraction or migration was so common in study participants that the researchers made the decision to stop implanting these devices at their institutions. The FDA joins the researchers in urging doctors and patients to thoroughly review the risks associated with the Bard IVC Filters before using them, and to make sure the implants are removed as soon as the risk of a blood clot has passed.

A number of patients who have suffered injury and the families of patients who died as a result of Bard IVC Filter complications have opted to file defective medical device lawsuits in pursuit of compensation for medical bills and other damages. In these medical product liability lawsuits, attorneys argue that C.R. Bard was aware of the high rate of risks associated with the medical device, but that they continued to make and market the products without properly informing consumers of these risks. Contact our Bard IVC Filter Lawsuit Attorneys If you or someone you love was harmed or killed as a result of implantation with a Bard IVC Filter system, you may be entitled to pursue compensation in a medical product liability lawsuit. Our Bard IVC Filter lawsuit attorneys can help you learn more about your rights in a free legal consultation.

Bard IVC Filter Injuries

Bard IVC filters can be victim to a number of problems or complications that may lead to serious injury or death. Some of the most prominent Bard IVC filter problems reported to the FDA include:

  • The filter migrates, or changes position
  • The filter becomes lodged in the body
  • The filter may perforate an organ, vessel, or tissue
  • The filter may fracture or break loose and travel to other organs such as the
    heart and lungs
  • The filter may become blocked
  • The filter may not be removable

These noted Bard IVC filter complications may lead to serious or life-

Threatening injuries, such as:

  • Cardiac tamponade
  • Heart perforation
  • Hemorrhagic pericardial effusion
  • Lung perforation
  • Vena cava puncture
  • Ventricular tachycardia

Bard IVC Filter Recall

At this time, the FDA is planning to review the safety and failure rate of Bard IVC filters to determine whether a recall of this potentially dangerous medical device is necessary. Physicians are now advised to make all patients aware of the risks associated with these devices. They should also be prepared to remove any Bard IVC filters as soon as the risk of clotting has passed.

A number of people who have suffered injury or loss as a result of Bard IVC filters have opted to file dangerous medical device product liability lawsuits against C.R. Bard, claiming that the company failed to warn patients and doctors of the risks associated with this product. If you or someone you love was injured after being implanted with a Bard IVC filter, you may be entitled to significant compensation. Contact a Bard IVC filter recall lawyer at our product liability law firm today to learn more about your rights in a free legal

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