Our Michigan Stryker OAYSYS spine implant recall attorneys filing lawsuits on behalf of patients suffering from serious complications, or having to undergo a revision surgery after having the recalled Stryker OAYSYS Occipito-Cervico-Thoracic System implanted. Patients who suffer from complications due to the defective nature of the cervical spine implant manufactured do have legal rights and may be able to pursue a lawsuit against the manufacturer for their injuries. Often times these lawsuits result in significant settlements for the patient.
Our Michigan defective medical device law firm is actively working with other national law firms to win the best settlement for our clients. We are actively representing patients against the manufacturer for complications related to the Stryker OAYSYS Occipito-Cervico-Thoracic System recall, or OASYS Midline Occiput Plate recall.
Stryker’s OASYS Midline Occiput Plate Recalled
OASYS Midline Occiput Plate is part of the OASYS Occipito-Cervico-Thoracic System used to promote fusion of the cervical spine and occipito-cervico-thoracic junction (Occiput – T3). The OASYS Midline Occiput Plate provides stabilization at the junction between the occipital bone and the vertebrae in the cervical spine.
The OASYS Midline Occiput Plate recall was issued after reports of the pin that connects the tulip head to the plate body fracturing and causing severe harm to those who had the system implanted.
The FDA issued a Class 1 recall on the device, indicating that using the device could result in serious injury or death. A Class 1 recall is one of the most serious warning labels the FDA distributes on a product.
The affected products being recalled were distributed from April 23, 2010, through February 12, 2013 and are listed below.
Manufacturing Part Number Product Description
48551044 OASYS MIDLINE OCCIPUT PLATE, SMALL
48551045 OASYS MIDLINE OCCIPUT PLATE, MEDIUM
48551046 OASYS MIDLINE OCCIPUT PLATE, LARGE
48551047 OASYS MIDLINE OCCIPUT PLATE, LARGE LONG
48551048 OASYS MIDLINE OCCIPUT PLATE, MINI
Stryker OAYSIS Spine Implant Recall Lawsuits
Due to the fact that Stryker Orthopaedics placed the OAYSYS Occipito-Cervico-Thoracic System on the market that included a part (Midline Occiput Plate) that is dangerous for the patient, the company may be held liable for damages caused by the implant. Patients who have suffered significant injuries from the recalled Stryker OAYSYS Occipito-Cervico-Thoracic System or OASYS Midline Occiput Plate do have legal rights to file a Michigan defective medical device lawsuit against the manufacturer. The lawsuits seek damages for pain and suffering, all medical costs incurred to date, medical expenses for any future treatment or surgery, lost wages, spousal damages, and punitive damages.
No Fee Promise for Michigan Stryker OAYSIS Spine Implant Recall Lawsuits
We will represent you in your Michigan Stryker OASYS Occipito-Cervico-Thoracic System lawsuit under our No Fee Promise. This means that you will not be charged any legal fees whatsoever unless we obtain a settlement or recovery for you. You have absolutely no obligation for legal fees unless we win your case. If we do not obtain a settlement for you, you owe us nothing!
Contact Your Michigan Stryker OASYS Spine Implant Lawyer
If you or someone you know had to undergo a revision surgery or suffers serious complications associated with the recalled OASYS Occipito-Cervico-Thoracic System or OASYS Midline Occiput Plate, call our top rated Buckfire & Buckfire, P.C. defective medical device attorneys now at (800) 606-1717. We will discuss your spine implant lawsuit and begin working on your case immediately, gathering all the medical records and evidence to prove and win your case. Call today and we will help determine if you have legal rights to file a claim against the manufacturer.