Musculoskeletal Transplant Foundation, Inc. FDA Recalls

4 recalls on file across devices, 0 of them Class I and 3 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)Class IIDec 22, 2023Filling process qualification did not demonstrate adequate p	Filling process qualification did not demonstrate adequate process capability. Possible consequences include e	Class IIDevices	Dec 22, 2023
AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)Class IIDec 22, 2023Filling process qualification did not demonstrate adequate p	Filling process qualification did not demonstrate adequate process capability. Possible consequences include e	Class IIDevices	Dec 22, 2023
DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defectClass IISep 22, 2023Units are labeled as 10cc; however the units have a fill vol	Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation	Class IIDevices	Sep 22, 2023
AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous dClass IIMar 29, 20213/4 AFT Straight Fill Tubes (227007) filled only 1/2 way in	3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may cause delay of surgery	Class IIDevices	Mar 29, 2021