Brand

Musculoskeletal Transplant Foundation, Inc. Recalls

6 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Musculoskeletal Transplant Foundation, Inc..

6Total Recalls
0Critical
369Units Affected
Dec 22, 2023Most Recent
All Recalls

Every Musculoskeletal Transplant Foundation, Inc. Recall

Sorted by most recent. Click any recall for full details.

6 recalls
High RiskFDA
Musculoskeletal Transplant Foundation, Inc.
AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
Medical Devices·89 affected·Dec 22, 2023
High RiskFDA
Musculoskeletal Transplant Foundation, Inc.
DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from tr...
Surgical Devices·18 affected·Sep 22, 2023
High RiskFDA
Musculoskeletal Transplant Foundation, Inc.
QuickGraft¿ Model # 430PST
Medical Devices·9 affected·Aug 15, 2019
High RiskFDA
Musculoskeletal Transplant Foundation, Inc.
Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created osseous defects or o...
Surgical Devices·114 affected·Apr 21, 2016
High RiskFDA
Musculoskeletal Transplant Foundation, Inc.
Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze.
Medical Devices·22 affected·May 27, 2015
High RiskFDA
Musculoskeletal Transplant Foundation, Inc.
Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific needs of the orth...
Surgical Devices·117 affected·May 27, 2015