Recall Atlas

Integrity Implants recalls

3 official recalls and safety alerts involving Integrity Implants since 2022-12, 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 Integrity Implants or the relevant agency.

  1. 2025-01-29
  2. US
    Drugs & medicalClass II

    Integrity Implants Inc. recalls Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product Description: The Repeater…

    Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).

    FDA · DeviceIntegrity Implants Inc.U.S. Nationwide distribution in the states of CA, F, GA, KY, LA, MA, MD, TN…Official notice →
  3. 2022-12-14
  4. US
    Drugs & medicalClass II

    Integrity Implants Inc. recalls LineSider Spinal System pedicle screws, 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Model Number LS-N6SG6545.…

    Potential for intraoperative screw head separation at weld location.

    FDA · DeviceIntegrity Implants Inc.US distribution to California, Indiana, New York, Oklahoma, Washington DCOfficial notice →
  5. US
    Drugs & medicalClass II

    Integrity Implants Inc. recalls LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Cannulated. Thoracolumbosacral pedicle screw system; Spinal…

    Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank.

    FDA · DeviceIntegrity Implants Inc.Nationwide distribution to AZ, CA, CT, DC, FL, IL, IN, LA, MA, MN, NJ, OK, PR,…Official notice →