Musculoskeletal Transplant Foundation, Inc.: Medical Device Recall in 2023 - (Recall #: Z-0323-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury. Model Number: 038100

Product Classification:

Class II

Date Initiated: September 22, 2023

Date Posted: November 29, 2023

Recall Number: Z-0323-2024

Event ID: 93296

Reason for Recall:

Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.

Status: Ongoing

Product Quantity: 18 units

Code Information:

GUID: W4184038100T0473 Serial #s: 002220854711400006 002220854711400056 002220854711400003 002220854711400008 002220854711400009 002220854711400001 002220854711400002 002220854711400010 002220854711400011 002220854711400012 002220854711400013 002220854711400014 002220854711400004 002220854711400005 002220854711400007 Exp.Date: June 20, 2025

Distribution Pattern:

US Nationwide distribution in the states of PA, TX, WA.

Voluntary or Mandated:

Voluntary: Firm initiated