DBX Mix — Class II medical device recall Z-1455-2015
Terminated recall by Musculoskeletal Transplant Foundation, Inc., reported 2015-04-29, distributed nationwide. The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for lot identified above may not be full
| Recall number | Z-1455-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc., Edison, NJ, United States |
| Recall initiated | 2014-12-04 |
| Classified | 2015-04-17 |
| Reported by FDA | 2015-04-29 |
| Terminated | 2017-05-08 |
| Distributed | Nationwide (US) |
| Quantity | 25 units |
| Reason classes | packaging |
Product
DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler.
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1455-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.