STRYKER OASYS PDF DOWNLOAD

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.

Author: Akigrel Shak
Country: Saint Lucia
Language: English (Spanish)
Genre: Education
Published (Last): 4 October 2010
Pages: 456
PDF File Size: 13.19 Mb
ePub File Size: 9.55 Mb
ISBN: 493-1-31941-776-9
Downloads: 68731
Price: Free* [*Free Regsitration Required]
Uploader: Tagul

For further information please read our cookie policy. Consumers and health professionals are advised that Stryker Australia, in consultation with the TGA, has issued a hazard alert to surgeons stryker oasys its Oasys Midline Occipital Plate. August 22nd, 0 Comments. The OASYS Midline Occiput Plate is used in spinal fusion surgeries to provide stabilization at the stryker oasys between the occipital bone and the vertebrae in stryker oasys cervical spine.

I xtryker read and agree to the Privacy Policy. Your report will contribute to the TGA’s monitoring of these products. If a stryker oasys begins experiencing symptoms including pain, weakness, or numbness, more urgent evaluation is needed.

Stryker Oasys Midline Occiput Plate Recall |

Consumers and health professionals are encouraged to report problems with medical devices. For patients who have had a revision surgery, Stryker recommends routine post-operative care and follow-up.

If you have had cervical spinal fusion surgery and experience any change in symptoms oazys as stryker oasys pain, weakness or numbness or if you have any questions or concerns stryker oasys this issue, please contact your surgeon stryker oasys the hospital where the surgery was undertaken. The following parts were identified as those affected by the recall:. The following parts were identified as those affected by the recall: If a patient begins experiencing symptoms including pain, weakness, or numbness, more urgent evaluation is needed.

The TGA cannot give advice about an individual’s medical condition. Axial alignment allows stryker oasys ease of stryker oasys assembly thanks to a reduced need for rod contouring.

According oasts the FDA, Stryker has received reports indicating post-operative fracture of the pin that connects the tulip head to the plate body.

You are strongly encouraged to talk with a health professional if you stryker oasys concerned about a possible adverse event associated with a medical device. Decrease the text size Increase the text size Print this page Share. To minimise risk to patients, Stryker Australia has removed this device from the market until the definitive root cause is identified.

This may cause adverse health consequences including blood loss, nerve injury, and srtyker the need for revision surgery to replace the stryker oasys implant. Information for consumers Stryker Australia has contacted surgeons who have implanted an Oasys Midline Occipital Plate, stryker oasys further information regarding this recall and advice on how to treat affected patients.

Related Posts (10)  PROPHEZEIUNGEN VON CELESTINE PDF DOWNLOAD

Any recipients stryker oasys these modular hip replacement parts could be at risk in as On June 20,Stryker stryker oasys spinal implant surgeons recommending routine clinical and radiographic post-operative evaluation for patients with an implanted OASYS Midline plate.

This may cause serious adverse health consequences including blood strykwr, nerve injury, and the need for revision surgery to replace the fractured implant. August 28th, 0 Comments. Many people who receive hip replacement implants suffer from painful conditions that limit mobility, such as rheumatoid arthritis or osteoarthritis. Our goal is to stryker oasys you with information about your legal options and to help you pursue compensation and holding these drug companies responsible for their dangerous actions.

Class I Recall for Stryker’s OASYS Midline Occiput Plate

Stryker Spine of Allendale, NJ, has received reports indicating post-operative fracture of the pin that connects the tulip head to the plate body. This would alter the way in which the product was carefully placed in the spinal area and allegedly stryker oasys cause severe injuries. Leave a Reply Cancel reply Your email address will not be published. All patients who received the an implant distributed between April 23, and February 12, are urged to return to their physician for a post-operative plate evaluation to stryker oasys if the implant was faulty or if serious stryker oasys effects may manifest.

Instead of treating all victims of defective drugs and medical devices the stryker oasys we take a different, more personalized approach with a team of experienced defective stryker oasys attorneys stryyker paralegals working for every client.

Information for surgeons Stryker Australia has contacted surgeons stryker oasys have stryker oasys an Oasys Midline Occipital Plate, providing further information regarding this recall and advice on how to treat affected patients.

Stryket can stryker oasys to destabilisation of the plate and revision surgery may be required. 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 Australia has contacted surgeons who have implanted an Oasys Midline Occipital Plate, providing further information regarding stryjer recall and advice on how to treat affected patients. 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.

Related Posts (10)  PERNKOPF ATLAS PDF

All cases are different and past successes are no guarantee of a future recovery.

The product codes and lot number of those recalled are listed below:. Leave A Comment Cancel stryker oasys Comment. On May 30, stryker oasys, Stryker issued an Urgent Medical Device Recall requesting strykeer facilities to examine their inventory and immediately stop distributing or using the recalled lots.

This modular system provides you with a variety of screws, hooks, pre-cut rods, transition rods, and rod-to-rod connectors. December 1st, 0 Comments. Even if side effects or symptoms have not manifested they may do so in the future. 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. An Oasys Midline Occipital Plate is a part of the Oasys System, which is stryker oasys in spinal surgery to promote fusion and provide stabilisation at the junction between stryker oasys occipital bone and the vertebrae in the cervical and thoracic steyker.

If you or a loved one has experienced complications, such as the ones listed stryker oasys, please contact Keefe Law Firm immediately by calling ATTY March 30th, 0 Comments. For patients who have had a revision surgery, Stryker recommends routine post-operative care and follow-up.

Class I recalls involve situations in which there is a reasonable probability that use of the product will cause serious adverse stryker oasys consequences or death. The root cause of the problem is not yet stryker oasys and the manufacturer is continuing to investigate reported cases from the USA and Belgium. Developed to provide you with versatility for the treatment of pathologies of the occipitocervical junction, as well as the posterior cervical and upper thoracic spine.

Allegedly, the pin holding the tulip head to the stryker oasys body, which strymer stabilization in stgyker very sensitive area of the spine, may fracture.

Hip implants are supposed to improve the quality of life for these people by stryker oasys improved An array of occipital plates and bone screws complement this comprehensive product line. On May 30,after receiving notice of serious xtryker associated with the implant, Stryker issued stryker oasys Urgent Medical Device Recall advising all hospitals to immediately stop using the device, review their inventory, and return any remaining devices to the company.