Kyler K., an Alabama resident, has joined more than 1,400 others in a lawsuit against C.R. Bard for problems allegedly tied to the company’s inferior vena cava (IVC) filter, which his lawsuit says failed. Kyler was implanted with a Meridian IVC filter on April 23, 2013. This model is a fifth generation temporary design that was approved for sale in 2011. The U.S. Food and Drug Administration (FDA) recommends that temporary, or retrievable, IVC filters be removed between 29 and 54 days.. However, in many cases, if the filter has migrated or perforated the vein, the device is rendered impossible to retrieve. The risk of injury ... Read More
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