Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The seal on the DBX Mix outer PETG/Aclar...

Date: December 4, 2014
Company: Musculoskeletal Transplant Foundation, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Musculoskeletal Transplant Foundation, Inc. directly.

Affected Products

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

Quantity: 25 units

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Musculoskeletal Transplant Foundation, Inc.

Musculoskeletal Transplant Foundation, Inc. has 9 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report