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 Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically Recalled by Musculoskeletal Transplant Foundation, Inc. Due to Units are labeled as 10cc; however the units...

Date: September 22, 2023
Company: Musculoskeletal Transplant Foundation, Inc.
Status: Ongoing
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 Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury. Model Number: 038100

Quantity: 18 units

Why Was This Recalled?

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

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