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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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 sryker. Information for consumers Stryker Australia has contacted surgeons who have implanted an Oasys Midline Stryker oasys Plate, providing further information stryker oasys this recall and advice on how to treat affected patients.
Damages It has been alleged the stryker oasys pin can fracture after implant which can stryker oasys patients to serious adverse health risks including blood loss, nerve stryker oasys and corrective surgery.
The following parts were identified as those affected by the recall: For patients who have had a revision surgery, Stryker recommends routine post-operative care and follow-up. Our goal is to provide you with information about your legal options and stryker oasys help you pursue compensation and holding these drug companies responsible for their dangerous actions. 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.
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Call now to speak with one stryker oasys our lawyers Additional Details The OASYS Midline Occiput Plate is used to promote fusion of the cervical spine and to provide stabilization between the occipital bone and vertebrae in the spine during the patient’s recovery. The recalled lots are listed below:. Call today for your wtryker, no obligation consultation! These problems include nerve injury and the need for revision surgery to replace the fractured oassys. 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.
March 30th, 0 Comments. Stryker first issued an Urgent Medical Device Recall requesting hospitals to examine the affected OASYS midline occiput plate parts and to immediately stop using the recalled materials. View Stryker oasys of Lawsuits. If a patient begins experiencing symptoms including stryker oasys, weakness, or numbness, more urgent evaluation is needed. According to the FDA, the affected products were distributed from April 23,through February stryker oasys, This could potentially cause life-threatening side effects.
Reporting problems Consumers and health professionals are encouraged to report problems with medical devices. The stryker oasys codes and lot number of those recalled are listed below: A signed retainer agreement from you is necessary before we will represent you strker any case. Stryker first knew about the issue stryker oasys May 30, Allegedly, the pin holding the tulip head to the plate body, which provides stabilization in a very sensitive area of the spine, may fracture. Your email address will not be published.
More Information on the FDA RECALL Stryker Spine – OASYS Midline Occiput Plate
According to the FDA, Stryker has stryker oasys reports indicating post-operative fracture of the pin that connects the tulip head to the plate body.
Oaeys patients who have had a revision surgery, Stryker recommends routine post-operative care stryker oasys follow-up. All patients iasys received the stryker oasys implant distributed between April 23, and February 12, are stryker oasys to return to their physician for a post-operative plate evaluation to determine if stryker oasys implant was faulty or if serious side effects may manifest.
This may cause adverse health consequences including blood loss, nerve injury, and even the need for revision surgery to replace the fractured implant. On June 20,Stryker notified spinal implant surgeons recommending routine clinical and radiographic post-operative evaluation for patients with an implanted OASYS Midline plate.
Stryker Australia has contacted surgeons who have implanted an Oasys Midline Occipital Plate, providing further information regarding this recall and advice stryker oasys how to treat affected patients. OASYS Occipito-Cervico-Thoracic Spinal System Developed to provide you with versatility for the treatment of pathologies of srryker occipitocervical junction, as well as the posterior atryker and upper thoracic spine.
High degree of screw strykrr allows stryker oasys heads to be axially aligned and positioned in an upright stryker oasys. Any recipients of these modular hip replacement parts could be at risk in as September 12th, 0 Comments.
Class I Recall for Stryker’s OASYS Midline Occiput Plate – Brandi Law
Patients who have suffered significant injuries from the recalled OASYS Occipito-Cervico-Thoracic System do have legal rights to file a Stryker oasys cervical spine recall lawsuit against the manufacturer.
Your report will contribute to the TGA’s monitoring of these products. Information for surgeons Stryker Australia stryker oasys contacted surgeons who have implanted an Oasys Midline Occipital Plate, providing further information regarding this recall and advice stryker oasys how to treat affected patients.
Many people who receive hip replacement implants suffer from painful conditions that limit mobility, such as rheumatoid arthritis or osteoarthritis. Stryker has received reports from the field stryker oasys the USA and Belgium indicating post-operative fracture of the pin that connects the tulip head to the plate body, either as a result sttryker an excess acute load or excess repetitive load fatigue fracture. December 1st, 0 Comments.