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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Patients who have had cervical spinal fusion surgery and who have any questions or concerns about the above issue should be referred to their surgeon or to the hospital where the surgery was undertaken.
If a patient begins experiencing symptoms including stryker oasys, weakness, or numbness, more urgent evaluation is needed.
oawys If a patient begins experiencing symptoms including pain, weakness, or numbness, more urgent evaluation is needed. Nothing herein shall be considered legal advice nor shall establish any attorney-client relationship with this law firm or its attorneys.
On June 20,Stryker notified spinal implant surgeons stryker oasys routine clinical and radiographic post-operative evaluation for patients with an stryker oasys OASYS Midline plate. This may cause serious adverse health stryker oasys including blood loss, nerve injury, and the need for revision surgery to replace the fractured implant.
All cases are different and past successes are no guarantee of a future recovery.
More Information on the FDA RECALL Stryker Spine – OASYS Midline Occiput Plate
This could potentially cause life-threatening side effects. Information for consumers Stryker Australia strykfr contacted surgeons who have implanted an Oasys Midline Occipital Plate, providing further information regarding this recall stryker oasys advice on how to treat affected strykef. An array of occipital plates and bone screws complement this comprehensive product line.
Attorneys at Keefe Law Firm are available for free legal consultations to victims of stryker oasys spinal stryker oasys implant failures. Class I recalls involve situations in which there is a reasonable probability that use of the product will cause serious adverse health consequences or death.
However, a month later, in Stryker oasys ofStryker put out a release warning to all surgeons stryker oasys conduct post-op evaluations on patients who already have had an OASYS implant. If you or a loved one has experienced complications, such as the ones listed above, stryker oasys contact Keefe Law Firm immediately by calling ATTY If you continue to browse this website, we will assume that you are happy to receive all our cookies.
The product codes and lot number of those recalled are listed below:. Before commenting, please review our comment policy. This plate is used to provide stabilization in the cervical spine; however reports are proving osays stryker oasys part of the system is causing significant problems to patients due to its defectiveness and possibility of fracturing.
Once the pin fractures, the tulip head may detach from the base of the device, potentially causing it to stryker oasys from its intended stryker oasys. The recalled lots are listed below: On June 20,Stryker notified spinal implant surgeons recommending routine clinical and radiographic post-operative evaluation for patients with an implanted OASYS Midline plate.
Related categories Neurotechnology Orthopaedics. If you have already implanted an Oasys Midline Occipital Plate, you are advised to stryler undertaking routine clinical and radiographic post-operative evaluation of your patients. The product codes and lot number of those recalled are listed below: The following parts were identified as those affected by the recall:.
If a patient with an Oasys Midline Occipital Plate reports or exhibits any change in symptoms, such as increased pain, weakness or numbness, more urgent evaluation should be undertaken.
According to the Stryker oasys, the affected products were distributed from April 23,through February 12, At stryker oasys time of this hazard alert, no cases of this problem had been reported in Australia. During a fusion procedure, the OASYS Stryker oasys Occiput Plate is implanted to provide stabilization at the junction between the occipital bone and the vertebrae in the cervical spine.
If you have had cervical spinal fusion surgery stryker oasys experience styrker change in symptoms such as increased pain, weakness or stryker oasys or if you have any questions or concerns about this issue, please contact stryker oasys surgeon or the hospital where the surgery was undertaken. Stryker first knew about the stryler on May 30, OASYS Occipito-Cervico-Thoracic Spinal System Developed to provide you with versatility for the treatment of pathologies of the occipitocervical junction, as well as the posterior stryker oasys and strykwr thoracic spine.
On June 20,Stryker notified spinal implant surgeons recommending routine oasyw and radiographic post-operative evaluation stryker oasys patients with an implanted OASYS Midline plate. The delicate area of the body in which this surgery occurs requires precise placement of the device, and should the device shift, it could pose risk of damage to the spinal cord.
This may cause adverse health consequences including blood loss, nerve injury, and even the need for revision surgery to replace the fractured implant. View List of Lawsuits. Leave A Comment Cancel reply Comment. Keefe Law Firm handles complex medical device implant litigation throughout the stryker oasys. Call today for your free, no obligation consultation!
The recalled lots are listed below:. For patients who stryker oasys had a revision surgery, Stryker recommends routine post-operative care and follow-up.
The affected devices that are being stryker oasys were distributed from April 23,through February 12, Hip implants are supposed to improve the quality of life for these people by granting improved Related information About recall actions.
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, stryker oasys punitive damages.