Health knowledge and news provided by doctors.

Shareholders File Medtronic Infuse Bone Graft Class Action Lawsuit

Armen Hareyan's picture

As a result of false statements which failed to disclose issues with their liquid bone stimulator, a Medtronic Infuse Bone Graft class action lawsuit has been filed by shareholders of Medtronic, Inc. The complaint alleges that Medtronic failed to disclose that a large portion of their revenue with the Infuse Bone Graft was from “off-label” sales and hid the fact that Medtronic was unlawfully marketing and encouraging use of the product for unapproved applications.

The class action lawsuit stems from recent reports of an investigation by the Justice Department that suggest Medtronic was actively marketing and promoting their bone stimulator for use in the cervical spine and other unapproved uses, which have been associated with a high rate of complications, such as compression of the airway or nerves, and possible death.

The Medtronic Infuse Bone Graft is only approved for use in the lumber spine and for certain dental procedures. It is designed to avoid the need to harvest bone from the hip, using a liquid bone stimulator, known as human bone morphogenetic protein, or BMP, to encourage bone growth and help replace spinal disks that are damaged.

Due to the close proximity between the cervical spine and the airway, use of the Medtronic bone graft during neck fusions could cause problems like:

Follow eMaxHealth on YouTube, Twitter and Facebook.
Please, click to subscribe to our Youtube Channel to be notified about upcoming health and food tips.

* Difficulty Breathing
* Difficulty Swallowing
* Difficulty Speaking
* Nerve Damage
* Death

The Medtronic Infuse Bone Graft class action lawsuit was filed on behalf of investors who were shareholders of Medtronic, Inc. between November 19, 2007 and November 17, 2008, alleging that the company concealed and failed to disclose the extent of their Infuse Bone Graft problems and the degree to which their revenue for the flagship product was reliant on “off-label” use and their illegal promotion.


For cervical fusion or neck surgery patients who have been injured as a result of the off-label use, the Medtronic Infuse Bone Graft lawyers at Saiontz, Kirk & Miles, P.A. are investigating and reviewing the potential for lawsuits on behalf of individuals throughout the United States. If you, a friend or family member have experienced problems, request a free consultation and claim evaluation.

Reprinted from http://www.youhavealawyer.com/



I had disc fusion surgery in 3/07 in which my surgeon used the artificial disc with BMP. I had major complication with swelling immediately after surgery. I had to be emergency trached and transported to local hospital. I went through a second surgery to put in a more stable breathing tube. I was put on a respirator and had my lung collapse 2X. I was in ICU for 7 days. I was lead to believe by my surgeon that the problems were a result of an allergic reaction to the anethisia, due to my weight or due to sleep apnea. I have been living with these explanations until I saw the Wall Street Journal article that discussed the reaction that patients had that were similar to mine. I still have major nerve problems that could be a result of the trashing around that I did when my airway was obstructed before they could secure a trach. I am in more pain today and will likely not be able to work in the near future. While the statute of limitations is up I was hoping that since we have new information about what caused the problem that possibly we have a case. Please advise. Kelly Williams [email protected] 513-947-8330