# FDA recall Z-1067-2024

> **Musculoskeletal Transplant Foundation, Inc.** · Class II · device recall initiated 2023-12-22.

## Product

AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)

## Reason for recall

Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.

## Distribution

Product was distributed to Minnesota.

## Key facts

- **Recall number:** Z-1067-2024
- **Recalling firm:** Musculoskeletal Transplant Foundation, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-22
- **Report date:** 2024-02-21

- **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-1067-2024

## Citation

> AI Analytics. FDA recall Z-1067-2024. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1067-2024. Source: US FDA. Licensed CC0.

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