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Musculoskeletal Transplant Foundation Recalls
9 recalls on record · April 29, 2015 to February 21, 2024 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 21, 2024Medical DevicesFDA
Musculoskeletal Transplant Foundation, Inc. recalls AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)
Hazard: Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
February 21, 2024Medical DevicesFDA
Musculoskeletal Transplant Foundation, Inc. recalls AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
Hazard: Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
November 29, 2023Medical DevicesFDA
Musculoskeletal Transplant Foundation, Inc. recalls DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defect
Hazard: Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.
May 19, 2021Medical DevicesFDA
Musculoskeletal Transplant Foundation, Inc. recalls AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous d
Hazard: 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may cause delay of surgery
October 2, 2019Medical DevicesFDA
Musculoskeletal Transplant Foundation, Inc. recalls QuickGraft¿ Model # 430PST
Hazard: Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.
July 13, 2016Medical DevicesFDA
Musculoskeletal Transplant Foundation, Inc. recalls Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created oss
Hazard: AFT Diverted Tubes are being recalled due to a customer complaint involving one unit which had an unsealed Tyvek pouch. The non-sterile foil pouch may introduce contamination into the sterile field.
August 5, 2015Medical DevicesFDA
Musculoskeletal Transplant Foundation, Inc. recalls Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze.
Hazard: Musculoskeletal Transplant Foundation (MTF) is recalling one lot of MTF's Allograft Cortical Pins because the lot was labeled as a 2.0 mm diameter pin and it may contain a 2.4 mm diameter pin.
July 22, 2015Medical DevicesFDA
Musculoskeletal Transplant Foundation, Inc. recalls Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific
Hazard: Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix Insertion Kits because they are labeled as having a 2.0mm diameter drill however it may contain a 2.4 mm diameter drill.
April 29, 2015Medical DevicesFDA
Musculoskeletal Transplant Foundation, Inc. recalls DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler.
Hazard: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for lot identified above may not be fully intact.