# FDA recall D-0715-2022

> **Rock Town Distillery, Inc.** · Class II · drug recall initiated 2022-03-10.

## Product

ROCK TOWN - DISTILLERY - HAND SANITIZER, Alcohol Antiseptic 70%, Topical Solution packaged in  a) 375 mL (12.7 fl. oz.), NDC 74492-0002-1; b) 3785 mL/1 gallon NDC 74492-0002-2; c) 236 mL/8 oz. NDC 74492-0002-3; d) 473 mL/16 oz. NDC 74492-0002-4; Made in USA Rock Town Distillery, 1201 Main Street Little Rock, Arkansas 72202

## Reason for recall

CGMP Deviations: FDA analysis found product to contain acetal and acetaldehyde above specification limits.

## Distribution

Distributed in Arkansas USA

## Key facts

- **Recall number:** D-0715-2022
- **Recalling firm:** Rock Town Distillery, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-03-10
- **Report date:** 2022-03-30
- **Termination date:** 2023-08-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Little Rock, AR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0715-2022

## Citation

> AI Analytics. FDA recall D-0715-2022. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/D-0715-2022. Source: US FDA. Licensed CC0.

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