Musculoskeletal Transplant Foundation, Inc.
Edison, NJ
This page shows every FDA and USDA recall linked to Musculoskeletal Transplant Foundation, Inc.. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
9
Total Recalls
2014
First Recall
2024
Most Recent
AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)
Feb 9, 2024
· Device
Active
AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
Feb 9, 2024
· Device
Active
DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osse...
Nov 17, 2023
· Device
Active
AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or...
Mar 29, 2021
· Device
Terminated
QuickGraft
Model # 430PST
Aug 15, 2019
· Device
Terminated
Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-c...
Jun 16, 2016
· Device
Terminated
Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze.
Jul 24, 2015
· Device
Terminated
Allofix Insertion Kit, 2.0 mm, Single Drill,
Product Usage:
MTF Surgical Instruments are designed for the sp...
Jul 15, 2015
· Device
Terminated
DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler.
Apr 17, 2015
· Device
Terminated