Johnson//Becker is investigating claims for individuals who were implanted with the LINX medical device and experienced serious complications, negative side effects, or needed to pursue a revision surgery as a result of either the device or implant procedure.
Learn More: Do I Qualify to Participate in a LINX Management System Lawsuit?
Understanding LINX Product Complications
Here is our current understanding of the possible risks associated with LINX.
- According to the AGA, “The history of devices placed around the gastroesophageal junction reveals that erosion of devices into the lumen of the esophagus is a significant risk, and reports of LINX erosion are now emerging.”
- A Bloomberg news report stated that models implanted from 2018 to 2025 may be linked to higher migration rates.
- Due to a manufacturing error as reported on in the past, LINX products may break and pose safety risks to the patient including increased acid reflux, internal injury, and respiratory issues.
What is the LINX Reflux Management System?
The LINX Reflux Management System, or, LINX, is a medical device. It is a small, ring-shaped implant made up of magnetic beads and titanium wire that is placed around the ‘esophageal sphincter’ to prevent stomach acid from flowing back into the esophagus. It has been used to treat patients with Chronic Acid Reflux, (GERD.)
The device was developed and marketed for use in 2012 by Torax Medical and later acquired by Ethicon, a company under Johnson & Johnson.
2018 LINX Recall
While marketed as safe and minimally invasive, LINX has been related to serious complications, side effects, revision surgeries and a prior recall.
A 2018 recall by Torax (the original manufacturer) included numerous model numbers associated with a product defect as a direct result of a manufacturing malfunction. This Class 2 recall by the FDA was to ensure all improperly manufactured products were returned to the manufacturer as well as warn physicians to monitor LINX implanted patients to ensure timely treatment should complications arise.
Johnson & Johnson Stops Selling LINX Devices Outside the U.S. Market
More recently, Johnson & Johnson announced their withdrawal of the LINX device from markets outside the U.S. Johnson & Johnson continues to maintain this decision is due to a shift in their marketing practices, despite reports of growing concerns and complaints in regard to the safety of the product.
Potential LINX Side Effects & Complications
The following lists a few of the complications the lawyers at Johnson//Becker are investigating:
- LINX device migration
- LINX device breakage
- Increased acid reflux
- Digestion obstruction
- Respiratory complications
- Esophageal erosion
- Chronic pain around the device location
- Organ damage
- Internal punctures
- And other internal injuries
If you or a loved one were implanted with the LINX Reflux Management System and believe you may be experiencing one of the above listed complications, you should talk with your doctor or a healthcare professional immediately.
Do I Qualify to Participate in a LINX Lawsuit?
We are investigating claims for individuals who underwent the LINX procedure for GERD or acid reflux and later experienced:
- LINX removal or revision surgery
- Organ damage, punctures, esophageal erosion
- Other serious complications
Why Choose Johnson//Becker for Your LINX Lawsuit?
Johnson//Becker is dedicated to serving you or your family with care, compassion, and commitment. Our lawyers have significant legal qualifications and over two decades of experience to best represent your interests in matters of injury due to medical devices.
Learn More: Why Choose Us
Questions About a LINX Lawsuit? Contact a Johnson//Becker Lawyer for a Free Case Review.
If you or a loved one were injured or adversely affected by LINX, you may want to speak with the lawyers at Johnson//Becker. We are currently accepting LINX lawsuits nationwide, and you may be entitled to financial compensation.
We offer a Free Case Evaluation. Please contact us using the form below or by calling us at (800) 279-6386.
We would be honored to speak with you and respond promptly to every inquiry we receive.
Free Case Evaluation
To contact us for a free review of your potential case, please fill out the form below or call us toll free 24 hrs/day by dialing: (800) 279-6386.