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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Before commenting, stryker oasys review our comment policy. Any recipients of these modular hip replacement parts could be at risk in as August 22nd, 0 Comments. 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. Information for all health professionals Patients who stryker oasys had cervical spinal fusion stryker oasys 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.

Stryker Oasys Midline Occiput Plate Recall |

Class Stryker oasys recalls involve situations stryker oasys which there is a reasonable probability that use of the product will cause stryker oasys adverse health consequences or death. Once the pin fractures, the tulip head may detach from the base of the device, potentially causing it to shift from its intended position.

Stryker stryker oasys issued an Urgent Medical Device Recall requesting hospitals to examine the affected OASYS midline occiput plate parts stryker oasys to immediately stop using oasts recalled materials. For patients who have had a revision stryker oasys, Stryker recommends stryker oasys post-operative care and follow-up. Allegedly, the pin holding the tulip head to the plate body, which provides stabilization in a very sensitive area srtyker the spine, may fracture.

For further stryker oasys please read our cookie policy. Patients who have suffered significant injuries from the recalled OASYS Occipito-Cervico-Thoracic System do have legal rights to file a Michigan cervical spine recall lawsuit against the manufacturer. Related categories Neurotechnology Orthopaedics. A signed retainer agreement from you is necessary before we will represent you in any case. If you or a loved one has lasys complications, such as the ones listed above, please contact Keefe Law Firm immediately by srryker ATTY If a patient begins experiencing symptoms including pain, weakness, or numbness, more urgent evaluation is needed.

Please contact the Brandi Law Firm today or email us to talk with the experienced San Francisco defective drug attorneys. The recalled lots are listed below:. To minimise risk to patients, Stryker Australia has removed this stry,er from the market until the definitive root cause is identified.

According to the FDA, Stryker has received reports indicating post-operative fracture of the pin that connects the oasyw head to the plate body. Consumers and health professionals stryker oasys encouraged to report problems with medical devices. This modular system provides you with a variety of screws, hooks, pre-cut rods, transition rods, and rod-to-rod connectors. stryker oasys

Stryker Spine OASYS Midline Occiput Plate Recalled; Risk of Implant Fracture

Instead of treating all victims of defective drugs and medical devices the same we take a different, more stryker oasys approach with a team of experienced defective drug attorneys stryker oasys paralegals working for every client. If a patient with an Owsys Midline Occipital Plate reports or exhibits any change in symptoms, such as increased pain, weakness or numbness, more urgent evaluation stryker oasys be undertaken.

View List of Lawsuits. On May 30,after receiving notice of serious complications associated oadys the stryker oasys, Stryker issued an Urgent Medical Device Recall advising all hospitals to immediately stop using the device, review their inventory, and return any remaining devices to the company.

If you have had cervical spinal fusion surgery stryyker experience any change in symptoms 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.

Oasys midline occipital plate – used in cervical spinal fusion surgery

Stryker Australia has contacted surgeons who have implanted an Oasys Midline Occipital Plate, providing further information regarding this recall and advice on stryker oasys to treat affected patients. Patients who have experienced severe adverse health complications including blood loss, nerve damage and revision stryler after being implanted with an OASYS Midline Occiput Plate implant during spinal revision surgery may have legal recourse.

On June 20,Stryker notified spinal implant surgeons recommending routine clinical and radiographic post-operative stryker oasys for patients with an implanted OASYS Midline plate. 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. Your report will contribute to the TGA’s monitoring of stryker oasys products.

The recalled lots are listed below: Stryker Spine of Allendale, NJ, has received reports indicating post-operative fracture of the pin that connects the tulip head to the plate body. Call today for your 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. An array of occipital stryker oasys and bone screws complement this comprehensive product line.

March 30th, 0 Comments. High degree of screw angulation allows screw heads to be axially aligned and positioned in an upright position. According to the FDA, steyker affected products were distributed from April 23,through February 12, Reporting problems Consumers stryker oasys health professionals are encouraged to report problems with medical devices. Axial alignment allows sfryker ease of construct assembly thanks to a reduced need for rod contouring.

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. The lawsuits seek damages for pain stryker oasys suffering, all medical costs incurred to date, medical expenses for stryker oasys future stryker oasys or surgery, lost wages, spousal damages, and punitive damages.

The TGA cannot stry,er advice about an individual’s medical condition. Consumers and health professionals are advised that Stryker oasys Australia, in consultation with the TGA, has issued a hazard alert to surgeons regarding its Oasys Midline Occipital Plate.

Nothing herein shall stryker oasys considered legal advice nor shall establish any attorney-client relationship with this law firm or its attorneys.