# FDA recall Z-2548-2019

> **Musculoskeletal Transplant Foundation, Inc.** · Class II · device recall initiated 2019-08-15.

## Product

QuickGraft¿  Model # 430PST

## Reason for recall

Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.

## Distribution

NY  NC  LA  TX  MO  OH

## Key facts

- **Recall number:** Z-2548-2019
- **Recalling firm:** Musculoskeletal Transplant Foundation, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-15
- **Report date:** 2019-10-02
- **Termination date:** 2020-07-01

- **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-2548-2019

## Citation

> AI Analytics. FDA recall Z-2548-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2548-2019. Source: US FDA. Licensed CC0.

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