OASYS is a comprehensive posterior Occipito-Cervico-Thoracic System designed to provide seamless junctional connections and a variety of fixation options. Consult Stryker’s entire OASYS® catalogue on MedicalExpo. Page: 1/ Data on file at Stryker Spine. Transition Rods. • mm to , , or mm. • mm in length with mm of. mm diameter and mm of larger diameter.
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Stryker Spine OASYS Midline Occiput Plate Recalled; Risk of Implant Fracture
View List of Stryker oasys. For patients who stryker oasys had a revision surgery, Stryker recommends routine post-operative care and follow-up. According to aosys FDA, Stryker has received reports indicating post-operative fracture of the pin that connects the tulip head to the plate body.
High degree of screw angulation allows screw heads to be axially aligned and positioned in an upright position. Call today for your free, no obligation consultation!
On June 20,Oawys stryker oasys spinal implant surgeons recommending routine clinical and radiographic post-operative evaluation for patients stryker oasys an implanted OASYS Midline plate.
Information for surgeons Stryker Australia has contacted surgeons who have implanted an Oasys Midline Occipital Plate, providing further information regarding this recall and advice on how to treat affected patients.
March 30th, 0 Comments.
If you or a loved one has experienced complications, such stryker oasys the ones listed above, please contact Keefe Law Firm immediately by calling ATTY Our goal is to provide you with information about your legal options and to help you pursue compensation and holding these drug companies responsible for their dangerous actions. This modular system provides you with a variety of screws, hooks, pre-cut rods, transition rods, and rod-to-rod connectors.
Many people who receive hip replacement implants suffer from painful conditions that limit mobility, such as rheumatoid arthritis or osteoarthritis. Related information About recall stryker oasys.
Allegedly, the pin holding the tulip head stryker oasys the plate body, which provides stabilization in a very sensitive area of the stryker oasys, may fracture.
Stryker Oasys Midline Occiput Plate Recall
It has been identified that, after the surgery, iasys pin that connects the tulip head to the plate body can break. This could potentially cause life-threatening side effects. Stryker first issued an Urgent Medical Device Recall requesting hospitals to examine the affected OASYS midline stryker oasys plate parts and to stryker oasys stop using the recalled materials. According to a jury, both stryker oasys did not warn consumers about risks involved with using It is a device used in spinal surgeries.
Oays herein shall be considered legal advice nor shall establish any attorney-client relationship with this law firm or its attorneys.
Instead of treating all victims of defective drugs and medical devices the same we take a different, more personalized approach with a team stryker oasys experienced defective drug attorneys and paralegals working for every client.
Damages It has been alleged the device’s pin can fracture after implant which can expose patients to serious stryker oasys health risks including blood loss, nerve damage and corrective surgery. The product codes and lot number of those recalled are listed below:.
Leave a Reply Stryker oasys reply Your email address will not be published. These problems include nerve injury and the need for revision surgery to replace the fractured implant. If a patient with stryker oasys Oasys Midline Occipital Plate reports or exhibits any change in symptoms, oawys as increased pain, weakness or numbness, more urgent evaluation should be undertaken.
Your report will contribute to the TGA’s monitoring of these products. The product codes and lot number of stryker oasys struker are listed below: During a fusion procedure, the OASYS Midline Occiput Plate is implanted to provide stabilization at the junction stryker oasys the occipital bone and the vertebrae in the cervical spine.
Patients who have suffered dtryker injuries from the recalled OASYS Occipito-Cervico-Thoracic System do have legal rights to file a Michigan cervical spine recall lawsuit against the manufacturer. This may cause adverse health stryker oasys including blood loss, nerve injury, and even the need for revision surgery to replace the fractured implant. This can lead to destabilisation of the plate and revision surgery may be required.
An array of occipital oaeys and bone stryke complement this comprehensive product line. August 28th, 0 Comments. The following parts were identified as those affected by the recall: Reporting problems Consumers and health professionals are encouraged to report problems stryker oasys medical devices.
Attorneys at Keefe Law Firm are available for free legal consultations to victims of alleged spinal fusion implant failures.