# FDA recall Z-0323-2024

> **Musculoskeletal Transplant Foundation, Inc.** · Class II · device recall initiated 2023-09-22.

## Product

DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury.  Model Number: 038100

## Reason for recall

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

## Distribution

US Nationwide distribution in the states of PA, TX, WA.

## Key facts

- **Recall number:** Z-0323-2024
- **Recalling firm:** Musculoskeletal Transplant Foundation, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-22
- **Report date:** 2023-11-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Edison, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0323-2024

## Citation

> AI Analytics. FDA recall Z-0323-2024. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-0323-2024. Source: US FDA. Licensed CC0.

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