# FDA recall Z-1562-2021

> **Musculoskeletal Transplant Foundation, Inc.** · Class II · device recall initiated 2021-03-29.

## Product

AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine  Item Number: 227007

## Reason for recall

3/4 AFT Straight Fill Tubes (227007)  filled only 1/2 way instead of 3/4, may cause delay of surgery

## Distribution

US Nationwide distribution in the state of MN.

## Key facts

- **Recall number:** Z-1562-2021
- **Recalling firm:** Musculoskeletal Transplant Foundation, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-03-29
- **Report date:** 2021-05-19
- **Termination date:** 2023-04-27

- **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-1562-2021

## Citation

> AI Analytics. FDA recall Z-1562-2021. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1562-2021. Source: US FDA. Licensed CC0.

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