NuVasive recalls
3 official recalls and safety alerts involving NuVasive since 2022-08, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with NuVasive or the relevant agency.
- 2023-02-15
USNuVasive Inc recalls NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US
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.
FDA · DeviceNuVasive IncU.S. Nationwide distribution in the states of CA, FL, NC, OH, and TX.Official notice →- 2022-12-28
- US
NuVasive Inc recalls X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Potential that insert will be unable to disengage from the vertebral body replacement device/implant
FDA · DeviceNuVasive IncWorldwide - U.S. Nationwide distribution including in the states of NC, CA,…Official notice → - 2022-08-03
- US
NuVasive Inc recalls Description/Part: Simplify Disc Size 1, Ht 5/SM-5; Simplify Disc Size 1, Ht 6/SM-6; Simplify Disc Size 2, Ht 4/MD-4; Simplify Disc Size 2,…
Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the incorrect Global Trade Item Number (GTIN) on the Patient Label when scanned and may also contain the incorrect GTIN human readable text,…
FDA · DeviceNuVasive IncUS: CA, WA, TX, IN, MO, MI, FL, VA, OR. OUS: DE, NZ, SG, UKOfficial notice →