Musculoskeletal Transplant Foundation recalls

Musculoskeletal Transplant Foundation appears in 9 official U.S. recall notices indexed by RecallRadar, most recently on 2024-02-21.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
  FDA Device · Class II · 2024-02-21 · Musculoskeletal Transplant Foundation
• AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)
  FDA Device · Class II · 2024-02-21 · Musculoskeletal Transplant Foundation
• DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from trau…
  FDA Device · Class II · 2023-11-29 · Musculoskeletal Transplant Foundation
• AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from…
  FDA Device · Class II · 2021-05-19 · Musculoskeletal Transplant Foundation
• QuickGraft¿ Model # 430PST
  FDA Device · Class II · 2019-10-02 · Musculoskeletal Transplant Foundation
• Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created osseous defects or oss…
  FDA Device · Class II · 2016-07-13 · Musculoskeletal Transplant Foundation
• Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature
  FDA Device · Class II · 2015-08-05 · Musculoskeletal Transplant Foundation
• Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific needs of the orthopedic…
  FDA Device · Class II · 2015-07-22 · Musculoskeletal Transplant Foundation
• DBX Mix, 20 cc, Product Code: 058200
  FDA Device · Class II · 2015-04-29 · Musculoskeletal Transplant Foundation