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All product recalls associated with NuVasive Specialized Orthopedics, Inc..
Total Recalls
14
Past Year
0
Class I (Serious)
0
Most Recent
Sep 2024
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Due to potential issues with design, manufacturing and documentation issues related to the validation of the affected products/devices.
Potential that insert will be unable to disengage from the vertebral body replacement device/implant
During accelerated shelf-life extension studies it was noted that the final packaging was experiencing a potential of failure of the sterile packaging barrier which could result in a hazardous situation where the device is no longer sterile.