Musculoskeletal Transplant Foundation, Inc. DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler. Recall
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler.
Brand
Musculoskeletal Transplant Foundation, Inc.
Lot Codes / Batch Numbers
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
Products Sold
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
Musculoskeletal Transplant Foundation, Inc. is recalling DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler. due to The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for lot identified above may not be fully intact.. This is a Class I recall, indicating a high risk of serious health consequences or death. Based on FDA medical device enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for lot identified above may not be fully intact.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 12, 2026