Musculoskeletal Transplant Foundation, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1067-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)

Product Classification:

Class II

Date Initiated: December 22, 2023

Date Posted: February 21, 2024

Recall Number: Z-1067-2024

Event ID: 93853

Reason for Recall:

Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.

Status: Ongoing

Product Quantity: 50

Code Information:

UDI-DI: W4184227005T0473 Donor Lots 00322029241137 and 00322039641144

Distribution Pattern:

Product was distributed to Minnesota.

Voluntary or Mandated:

Voluntary: Firm initiated