Musculoskeletal Transplant Foundation, Inc.: Medical Device Recall in 2015 - (Recall #: Z-1455-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler.

Product Classification:

Class II

Date Initiated: December 4, 2014

Date Posted: April 29, 2015

Recall Number: Z-1455-2015

Event ID: 70739

Reason for Recall:

The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for lot identified above may not be fully intact.

Status: Terminated

Product Quantity: 25 units

Code Information:

064130067910690008; 064130067910690009; 064130067910690004; 064130067910690023; 064130067910690024 064130067910690005; 064130067910690015; 064130067910690016; 064130067910690018; 064130067910690020; 064130067910690007; 064130067910690013; 064130067910690028; 064130067910690029; 064130067910690030; 064130067910690010; 064130067910690006; 064130067910690011; 064130067910690012; 064130067910690019; 064130067910690021; 064130067910690014; 064130067910690017; 064130067910690001; 064130067910690022

Distribution Pattern:

US Nationwide distribution to CA, KY, IL, LA, PA, NC, TN, WV, and Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated