LINX Acid Reflux Implant Lawsuit | 2025 Latest Updates

What’s the Problem?

The Linx Reflux Management System, a small ring of magnetic titanium beads implanted to treat chronic acid reflux, has been linked to serious safety concerns. Patients have reported device migration, mechanical failure, chronic pain, and the need for revision surgeries.

Reports to the FDA and litigation filings highlight risks of internal damage when the device breaks or erodes into the esophagus. Although lawsuits are still developing in the U.S., complaints are already surfacing from patients who required emergency interventions.

Although we are not aware of an active U.S. recall of Linx implants, lawsuits continue to emerge alleging that Johnson & Johnson and its subsidiaries failed to warn patients and surgeons of known device risks.

Latest Linx Implant Updates

• September 2025 – Johnson & Johnson announced it will withdraw the Linx Acid Reflux implant from markets outside the U.S. after increasing concerns from surgeons about breakage and migration risks [1]
• 2025 – Lawsuits filed in U.S. courts allege device failures caused revision surgeries and severe injuries, including erosion into the esophagus [2]
• 2024 – Patient Tilghman filed a lawsuit claiming defective materials used in Linx implants caused malfunction and surgical removal [2]
• Ongoing – The FDA’s recall database lists safety events involving the Linx system, including failure to open and close properly, leading to swallowing difficulties and pain [3]

Linx Implant Statistics

• Over 40,000 Linx devices have been implanted globally since FDA approval in 2012.
• Multiple peer-reviewed studies show complication rates leading to explantation in up to 7% of cases within 5 years.
• Reported injuries include device erosion, breakage, esophageal perforation, and chronic pain.
• Settlements and pending claims are expected to total millions in liability costs for manufacturers.

FDA Reports and Statistics

The FDA’s Manufacturer and User Facility Device Experience (MAUDE) database documents hundreds of adverse event reports tied to the Linx implant. Reported injuries include:

• Esophageal erosion or perforation
• Device breakage requiring revision surgery
• Persistent pain and difficulty swallowing

Regulators continue to monitor the device’s long-term safety, and litigation filings often cite FDA adverse event reports as supporting evidence of manufacturer knowledge.

Linx Implant Injuries & Side Effects

Patients have reported the following serious complications after implantation:

• Device migration – implant shifts from its intended position, damaging surrounding tissue
• Erosion into the esophagus – leads to internal injury and life-threatening risks
• Revision surgery – emergency removal due to device breakage or failure
• Chronic pain and swallowing difficulties – significantly impairing quality of life

Do You Qualify for a Linx Implant Lawsuit?

• You received a Linx Acid Reflux implant between 2012 and present
• You experienced serious side effects including erosion, migration, or device failure
• You required medical treatment, hospitalization, or revision surgery
• You can provide medical records documenting your device implantation and complications

Evidence Required for a Linx Implant Lawsuit

• Medical records showing implantation and diagnosis of complications
• Surgical records detailing explantation or revision
• Proof of device model and implant date
• Physician testimony connecting the device to your injuries

Damages You Can Recover

• Past and future medical expenses
• Lost wages and reduced earning potential
• Pain and suffering, including loss of enjoyment of life
• Wrongful death damages for surviving family members
• Punitive damages in cases of gross negligence

Linx Implant Recall Information

Although the FDA has not issued a formal U.S. recall of the Linx Acid Reflux Implant, Johnson & Johnson recently announced market withdrawals outside the United States. International regulators have flagged concerns about long-term safety, and recall-style actions may follow in the U.S. depending on litigation outcomes and ongoing FDA monitoring.

Statute of Limitations for Linx Implant Lawsuits

State deadlines for filing lawsuits vary, typically ranging from 1 to 4 years from the date of injury or discovery of harm. Patients should act quickly to preserve their rights, as missing the statute of limitations may forfeit the ability to recover compensation.

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Frequently Asked Questions

• What is the Linx Acid Reflux Implant? – A small ring of magnetic beads designed to treat GERD by preventing stomach acid from flowing back into the esophagus.
• Why are lawsuits being filed? – Patients allege device failure, breakage, and severe injuries that were not adequately disclosed by the manufacturer.
• Has the Linx Implant been recalled? – Not in the U.S., but Johnson & Johnson has withdrawn the device from some foreign markets.
• What compensation is available? – Medical costs, lost income, pain and suffering, and punitive damages may be pursued.
• How long do I have to file? – Deadlines vary by state, so immediate legal consultation is advised.

References

1. https://www.bloomberg.com/news/articles/2025-09-23/j-j-to-withdraw-acid-reflux-device-outside-us-alarming-surgeons
2. https://www.aboutlawsuits.com/linx-implant-lawsuit-over-device-failure-led-to-revision-surgery/
3. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=163595