Overview of recall records associated with NuVasive Inc., including dates, categories and classifications where available.
Classification mix: Class III: 1, Class II: 1.
Due to an incorrect security key, customers were unable to connect to remote monitoring during spinal surgery, neck dissections, thoracic surgeries, and upper and lower extremity procedures.
Potential that insert will be unable to disengage from the vertebral body replacement device/implant
This page summarizes recall records in which the official source identifies NuVasive Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
