LINX Reflux Lawsuit
Individuals who experienced complications after having the LINX device implanted to treat gastroesophageal reflux disease (GERD) are pursuing lawsuits, claiming that a manufacturing defect in the LINX devices may cause…
Individuals who experienced complications after having the LINX device implanted to treat gastroesophageal reflux disease (GERD) are pursuing lawsuits, claiming that a manufacturing defect in the LINX devices may cause…
More than 9,000 individuals who received a recalled LINX reflux device could be at risk of injuries and the need for removal surgery, lawsuit alleges.
Case joins a growing number of LINX lawsuits filed in recent months, each raising similar allegations that the loop of beads used to make the esophageal implant can break and migrate.
Multiple LINX Reflux lawsuits have been filed in recent months due to problems with the recalled devices breaking and requiring surgical removal
Lawsuit stems from a LINX recall announced by the FDA in 2018, due to the risk that the loop of titanium beads in the reflux management system may break inside the human body.