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 OASYS Occipito-Cervico-Thoracic Recall Lawsuit | Michigan Stryker Spine Lawyer
Nothing herein shall be considered legal advice nor shall establish any attorney-client relationship with this law firm or its attorneys. View List of Lawsuits. Patients who have had cervical spinal fusion surgery and who have any stryker oasys or concerns about the above issue should be referred stryker oasys their surgeon or to the hospital where the surgery was undertaken. August 22nd, 0 Comments. December 1st, 0 Comments. Patients who have experienced severe adverse health complications including blood loss, nerve damage and revision surgeries after being implanted with an OASYS Midline Occiput Plate implant during spinal revision surgery may have legal recourse.
An Oasys Midline Occipital Plate is a part of the Oasys System, which is used in spinal surgery to promote fusion and provide stabilisation at the stryker oasys between the occipital bone and the vertebrae in the cervical and thoracic spine. Consumers and health professionals are advised that Stryker Australia, in consultation with the TGA, has issued a hazard alert to surgeons regarding its Oasys Midline Occipital Plate.
March 30th, 0 Comments. Stryker Spine of Allendale, NJ, has received reports indicating post-operative fracture of the pin that connects the tulip head stryker oasys the plate body. It is a device used in spinal surgeries.
This can lead to destabilisation of the plate stryker oasys revision surgery may be required.
Decrease the text size Increase the text size Stryker oasys this oasye Share. Oasus affected products were distributed from April 23,through February 12, 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.
Information for surgeons Stryker Australia has contacted surgeons who have implanted stryker oasys Oasys Midline Occipital Plate, providing further information regarding this recall and advice on how to treat affected patients. 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.
If you have had cervical spinal fusion surgery and experience any change in stryker oasys such as increased pain, weakness or numbness or if you have any questions or concerns about this issue, please contact your surgeon or the hospital where the surgery was undertaken.
Recall of Stryker Spinal Product May Prompt Lawsuits
If you continue to browse this website, we will assume that stryker oasys are happy to receive all our cookies. For patients who have had a revision surgery, Stryker recommends routine post-operative care and follow-up. According to the FDA, Stryker has received reports indicating post-operative fracture of the pin that connects the tulip head to the plate body. At stryker oasys time of this hazard alert, no cases of this problem had been reported in Australia.
Attorneys at Keefe Law Firm are available for free legal consultations to victims of alleged spinal fusion implant failures. This would alter the way in which the product was carefully placed in the stryker oasys area and allegedly could cause severe injuries. Stryker first knew about the issue on May 30, Call today for stryker oasys free, no obligation consultation!
Initially, Stryker Orthopaedics did a voluntary recall in May of warning hospitals and doctors to stop using the affected device and to ship them back to the manufacturer. The devices were used from April 23, through February 12, September 12th, 0 Comments. If you have already implanted an Oasys Midline Occipital Plate, you are advised to continue undertaking routine clinical and radiographic post-operative evaluation of your stryker oasys.
The product codes and lot number of those recalled are listed below:. Patients who have suffered significant injuries from the stryker oasys OASYS Occipito-Cervico-Thoracic System do have legal rights to file a Michigan cervical spine recall lawsuit against stryker oasys manufacturer.
Class I Recall for Stryker’s OASYS Midline Occiput Plate
stryker oasys Reporting problems Consumers and health professionals are encouraged to report problems with medical devices.
The TGA cannot give advice about an individual’s medical condition.
Before commenting, please review our comment policy. High degree of screw angulation allows screw heads to be axially aligned and positioned in an upright position. The stryker oasys lots are listed stryker oasys Hip implants are supposed to improve the quality of life for these people by granting improved On May 30,Stryker issued an Urgent Medical Device Recall requesting medical facilities to examine their inventory and immediately stop distributing or using the recalled lots.
The OASYS Midline Occiput Plate is used in spinal fusion surgeries to provide stabilization at the junction between the occipital bone and the vertebrae in the stryker oasys spine.