Stryker OASYS Spinal Surgery Device Recalled, Australia Issues Hazard Alert Following Reports of Device Failure and Patient Injury
A Class I recall has been issued in the United States for the OASYS Midline Occipital Plate, part of the OASYS Occiptito-Cervico-Thoracic System. The device is used in cervical spinal fusion surgery. Class 1 recalls are the most serious, which the FDA says are “situations in which there is a reasonable probability that use of these products… Continue reading
