Every recall we track for NuVasive Inc — 5 in all — plus the complaints and injury reports the public filed about them.
NuVasive recalls X-Core 2 Ti Core implants used in spinal surgery due to potential inability to disengage from vertebral implants. Affected units have specific part numbers and lot codes. Consumers should contact NuVasive for details.
NuVasive recalls specific software versions for spinal surgery due to remote monitoring connection issues. Affected units may not connect to remote monitoring during critical procedures.
NuVasive recalls Simplify Disc models with incorrect UDI barcodes that could lead to selecting the wrong disc size during surgery. Affected units have specific part numbers and lot codes. Consumers should contact NuVasive for details.
NuVasive recalls NVM5 EMG Module (REF 8020015) due to incorrect component causing potential delay in spinal surgery monitoring. Affected units have specific model and lot numbers.
Recall of NuVasive MAGEC 2 spinal rods with specific lot numbers due to risk of internal component separation after implantation, potentially causing tissue discoloration.
