# FDA recall Z-2024-2021

> **Vivorte, Inc.** · Class II · device recall initiated 2018-09-09.

## Product

Vivorte Trabexus EB 10 cc Bone Void Filler  -Fill bone and/or defect in skeletal system  Model Number: 130703-10

## Reason for recall

incorrect expiration date- product is listed with 02-15-2019 the correct kit expiration date is 12-18-2018

## Distribution

US state of KY

## Key facts

- **Recall number:** Z-2024-2021
- **Recalling firm:** Vivorte, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-09-09
- **Report date:** 2021-07-14
- **Termination date:** 2021-11-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Louisville, KY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2024-2021

## Citation

> AI Analytics. FDA recall Z-2024-2021. Retrieved 2026-08-21 from https://api.ai-analytics.org/recall/Z-2024-2021. Source: US FDA. Licensed CC0.

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