NuVasive Specialized Orthopedics recalls

4 official recalls and safety alerts involving NuVasive Specialized Orthopedics since 2021-12, 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 Specialized Orthopedics or the relevant agency.

  1. 2024-11-27
  2. US
    Drugs & medicalClass II

    NuVasive Specialized Orthopedics, Inc. recalls Precice Max REF: PM10.0-80B265 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 265mm PM10.0-80B280 PRECICE MAX…

    Due to potential issues with design, manufacturing and documentation issues related to the validation of the affected products/devices.

    FDA · DeviceNuVasive Specialized Orthopedics, Inc.U.S distribution to states of: FL and NV.Official notice →
  3. 2022-12-21
  4. US
    Drugs & medicalClass II

    NuVasive Specialized Orthopedics, Inc. recalls NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to minimize the progression of…

    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…

    FDA · DeviceNuVasive Specialized Orthopedics, Inc.Distribution US nationwide including Puerto Rico; Chile, Israel, Jordan, New…Official notice →
  5. 2022-02-02
  6. US
    Drugs & medicalClass II

    NuVasive Specialized Orthopedics, Inc. recalls MAGEC 1 System

    Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015.

    FDA · DeviceNuVasive Specialized Orthopedics, Inc.WorldwideOfficial notice →
  7. 2021-12-08
  8. US
    Drugs & medicalClass II

    NuVasive Specialized Orthopedics, Inc. recalls NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product Description:…

    The Instructions for Use have been updated to include: (1) Clarification that the device is intended for use only in patients 18 years and older, (2) That patients should weigh 50 lbs. or more while undergoing…

    FDA · DeviceNuVasive Specialized Orthopedics, Inc.U.S.: AK, AL, AR, AZ, CA, CO, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA,…Official notice →