# FDA recall Z-2335-2021

> **BioMimetic Therapeutics, LLC** · Class II · device recall initiated 2021-07-23.

## Product

AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343

## Reason for recall

The kit contains the wrong vial tray in the package.

## Distribution

US Nationwide distribution in the states of AK, CA, CO, FL, GA, IA, ID, IL, IN, MA, MI, MN, NC, NJ, NM, NY, OH, OR, PA, TX, UT, VA, WA, and WI.

## Key facts

- **Recall number:** Z-2335-2021
- **Recalling firm:** BioMimetic Therapeutics, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-23
- **Report date:** 2021-09-01
- **Termination date:** 2024-09-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Franklin, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2335-2021

## Citation

> AI Analytics. FDA recall Z-2335-2021. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2335-2021. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*