Recall Atlas

Musculoskeletal Transplant Foundation recalls

2 official recalls and safety alerts involving Musculoskeletal Transplant Foundation since 2023-11, 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 Musculoskeletal Transplant Foundation or the relevant agency.

  1. 2024-02-21
  2. US
    Drugs & medicalClass II

    Musculoskeletal Transplant Foundation, Inc. recalls AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)

    Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.

    FDA · DeviceMusculoskeletal Transplant Foundation, Inc.Product was distributed to Minnesota.Official notice →
  3. 2023-11-29
  4. US
    Drugs & medicalClass II

    Musculoskeletal Transplant Foundation, Inc. recalls DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous…

    Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.

    FDA · DeviceMusculoskeletal Transplant Foundation, Inc.US Nationwide distribution in the states of PA, TX, WA.Official notice →