7 results

• GERD Implant Lawsuit Alleges Defective LINX Failed After Surgery

  October 5, 2026

  Michael Adams

  A Texas woman’s lawsuit claims she was implanted with a defective LINX reflux device months after it had been recalled over manufacturing problems.

• Recalled LINX Device Caused Recurrence of GERD Symptoms, Requiring Surgical Removal: Lawsuit

  August 12, 2026

  Irvin Jackson

  LINX GERD treatment implant had to be surgically removed after failing inside a patient's body, causing his acid reflux problems to return.

• Lawsuit Over LINX Device Complications To Be Prepared for Trial in May 2028

  June 1, 2026

  Irvin Jackson

  A woman’s lawsuit over a recalled LINX GERD treatment implant has been scheduled to go before a jury in May 2028, involving claims that the device was defectively designed and manufactured and caused serious complications.

• LINX Reflux Management System Lawsuit Alleges Implant Failed, Requiring Surgical Removal

  January 23, 2026

  Irvin Jackson

  A Texas man's LINX acid reflux device lawsuit says defendants manufactured a defective GERD implant that can break inside patients' bodies.

• LINX Device Recall Lawsuit Filed Over Risk of Bead Separation Complications

  December 9, 2025

  Michael Adams

  Amid a wave of LINX lawsuits tied to a 2018 recall for bead separation issues, a New Jersey man claims he underwent removal surgery after being implanted with a recalled device intended to treat his GERD.

• LINX Reflux Device Failed Due to Manufacturing Defect, Lawsuit Alleges

  November 24, 2025

  Michael Adams

  A Texas man’s lawsuit states that the LINX acid reflux device implanted in him was among more than 9,000 units recalled in May 2018, forcing him to undergo removal surgery earlier this month.

• LINX Implant Lawsuit Claims Recalled GERD Device Failed Due to Manufacturing Defects, Requiring Surgical Removal

  September 3, 2024

  Russell Maas

  A LINX implant lawsuit has been filed by a Pennsylvania woman who claims the esophageal implant to treat her GERD symptoms failed due to manufacturing defects, requiring her to undergo additional removal surgery.