Recall Atlas

Linkbio recalls

3 official recalls and safety alerts involving Linkbio since 2023-05, 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 Linkbio or the relevant agency.

  1. 2026-04-22
  2. US
    Drugs & medicalClass II

    Linkbio Corp. recalls LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

    The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.

    FDA · DeviceLinkbio Corp.US Nationwide distribution in the state of Alabama, Florida, and Kansas.Official notice →
  3. 2023-06-07
  4. US
    Drugs & medicalClass II

    Linkbio Corp. recalls LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for primary and revision…

    Contains the incorrect implant in the packaging. The packaging incorrectly contains the opposite side of the implant (Lateral-Right/Medial-Left instead of Medial-Right/Lateral-Left).

    FDA · DeviceLinkbio Corp.US Nationwide Distribution - AL, GA, IL, IN, LA, NV, TXOfficial notice →
  5. 2023-05-10
  6. US
    Drugs & medicalClass II

    Linkbio Corp. recalls LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X 58MM Item Number: 15-2028/13

    Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early aseptic loosening or increased wear of the implant caused by suboptimal…

    FDA · DeviceLinkbio Corp.NY, NV Foreign: Bulgaria, France, Italy, Norway, Poland, Sweden, Switzerland,…Official notice →