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IVC Filter Lawsuits

Lasers May Now Enable Doctors To Safely Retrieve Embedded IVC Filters

Bard IVC Filter Lawsuits

A new laser medical device was approved by the FDA the other day that could make it possible to remove IVC filters intact

Wednesday, December 22, 2021 - IVC filter removal, or the lack thereof, is the topic of hundreds of Bard IVC filter lawsuits that allege the manufacturer of the failed medical device was negligent in marketing the product to doctors and also failed to warn the public. The device use has declined in popularity recently as more and more complications come to light when it is left in the blood vessel too long. In 2010 the Food and Drug Administration (FDA) warned the medical community about the dangers of failing to retrieve an IVC filter promptly after only a few weeks. The FDA has addressed the complaints of those who have been injured by a faulty and defective IVC filter. The agency's warning told doctors and their assistants to remove the blood clot trapping device as soon as possible after the patient's risk of pulmonary embolism had passed. The FDA made this announcement after reviewing hundreds of reports made by doctors and patients that the IVC filter breaks apart during retrieval and pieces of the device migrate to damage other tissues and organs, sometimes the heart and lungs. Many times the fragments of the IVC filter were irretrievable and became permanently lodged in one of the internal organs. When this happens patients experience excruciating pain and must live with the fear of sudden death.

Bard IVC filter lawyers for plaintiffs suing Bard, the maker of the IVC filter, claim that a design defect caused the IVC filter to tilt and become permanently encased in scar tissue within the inferior vena cava, making it impossible to retrieve without breaking it. A new medical device was approved the other day by the FDA the other day that could make retrieving an intact IVC filter easier to do. the Philips CavaClear Laser Sheath, a laser cutting device, has received FDA approval for use in retrieving IVC filters that have become encapsulated in local scar tissue and are difficult to extract. The laser removes only a minimal amount of tissue and seals the wound as it moves inside the inferior vena cava. Bram Zuckerman, MD, director of the Office of Cardiovascular Devices in the FDA Center for Devices and Radiological Health Told MedPageToday.com about the excitement surrounding the device and also addressed the fears patients had in the IVC filter device. "To date, there have been limited options for the successful removal of chronically embedded IVC filters, as they can be difficult to retrieve due to potential complications associated with the complex procedure. The medical device approval was fast-tracked by the FDA which designated it as a "breakthrough medical device." The FDA designates a device to be a medical breakthrough if no approved or cleared alternative device exists, if it offers significant advantages over approved alternatives, of if using the device is in the best interest of patient. The new Philips CavaClear Laser Sheath appears to check all of the boxes.

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No-Cost, No-Obligation Bard IVC Filter Lawsuit Case Review for Persons or Families of Persons Who Suffered from Organ Damage, Severe Bleeding, Stroke, or Death

OnderLaw, LLC is a St. Louis personal injury law firm handling serious injury and death claims across the country. Its mission is the pursuit of justice, no matter how complex the case or strenuous the effort. The Onder Law Firm has represented clients throughout the United States in pharmaceutical and medical device litigation such as Pradaxa, Lexapro and Yasmin/Yaz, where the firm's attorneys held significant leadership roles in the litigation, as well as Actos, DePuy, Risperdal and others, and other law firms throughout the nation often seek its experience and expertise on complex litigation.