Patients who suffered from Medtronic Infuse problems after undergoing a cervical spine surgery with the product may have legal recourse to recover financial compensation for damages.

Reportedly, the company failed to properly disclose serious and potentially life-threatening infuse bone graft complications, which can include cyst formation and male infertility, potentially providing patients the opportunity to take legal action for their Medtronic Infuse problems. Medical bills and lost wages are among the damages which may be available to injured patients who seek recovery through Medtronic Infuse bone graft lawsuits.

Infuse Bone Graft Complications

Allegedly, Medtronic neglected to inform patients and doctors of serious Medtronic Infuse problems related to the product and promoted the use of the protein in a number of unapproved settings. The Medtronic Infuse Bone Graft has received FDA approval in lower spine-repair surgery to stimulate bone growth, but was not approved for use in the cervical spine, which runs from the shoulders to the head. Still, some patients have undergone a cervical spine surgery using the Infuse bone graft to treat neck pain; patients who underwent surgery with the bone graft in this setting may be at risk for serious infuse bone graft complications.

The FDA has received numerous reports of Medtronic Infuse problems associated with its use in cervical spine fusions, for which it has not received FDA approval. These Medtronic Infuse problems include difficulty swallowing, breathing and speaking, as well as swelling of the neck and throat tissue. Other Medtronic Infuse complications reportedly associated with the product include:

• Cyst formation
• Infection
• Cancer
• Infertility (sterility in men)
• Death