Understanding the Legal Theories Supporting LiabilityДЄ bone graft injury attorney in Grand Rapids or Traverse City can advise injured consumers on their options in pursuing compensation. This has led to numerous product liability cases against the manufacturer and other entities involved in distributing the device in Michigan and other states. Some patients have complained of chronic pain, weakness, abnormal bone growth, reproductive issues (in males), cancer, and difficulty speaking, swallowing, or breathing. Infuse Bone Graft, however, purports to produce new bone tissue at the site of implantation through the release of a genetically engineered version of the protein that regulates bone healing, which provides a вЂњscaffoldвЂќ into which new bone grows. Traditionally, when a patient needed a bone graft, his or her surgeon harvested bone from another part of the patientвЂ™s body. Medtronic Infuse Bone Graft may have been used off-label (for purposes other than those for which it received approval from the Food & Drug Administration), have been used incorrectly, have been implanted in some patients without their prior knowledge or consent, or simply be unreasonably dangerous.

The allegations against Medtronic are numerous and sometimes complex. If you or someone in your family has been treated with Medtronic Infuse Bone Graft and would like to know about your legal rights, the Traverse City and Grand Rapids bone graft injury lawyers at Neumann Law Group will be glad to take the time to discuss your options with you. This has led to not only several product liability lawsuits but also a stockholder derivative lawsuit filed by a disgruntled investor. Recently, there has been growing concern expressed by patients who received Medtronic Infuse Bone Graft products. Sometimes, a medical device may work for some patients but cause devastating or even potentially fatal complications for others, leaving some individuals in a more precarious state of health than before they were вЂњtreatedвЂќ with the drug or device. However, what is promised is not always what is ultimately delivered. It seems that doctors and medical scientists are always coming out with more impressive medical products and devices. Patients are particularly at risk for Infuse bone graft complications when undergoing cervical spine fusions, a procedure for which the product was not FDA-approved.Product Liability Lawyers Assisting Victims in Traverse City and Grand Rapids regulations and other publications found that up to 50% of patients suffered from Medtronic infuse problems, according to the Spine Journal. No infuse bone graft complications were reported in 13 clinical trials funded by the company, while data provided to U.S.

Reportedly, studies funded by the manufacturer neglected to disclose serious Medtronic Infuse problems. Infection, cyst formation, male infertility and death are among the serious Medtronic infuse problems reportedly associated with the product. The protein has only been FDA-approved for use in lower spine repair surgery to promote bone growth, and when used in cervical spine (upper spine and neck) surgery, may put the patient at risk for Infuse bone graft complications. Reportedly, the Medtronic Infuse bone graft can lead to serious complications when it is used in unapproved procedures.

Infuse lawsuits