Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

ROCK TOWN - DISTILLERY - HAND SANITIZER Recalled by Rock Town Distillery, Inc. Due to CGMP Deviations: FDA analysis found product to contain...

Date: March 10, 2022
Company: Rock Town Distillery, Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Rock Town Distillery, Inc. directly.

Affected Products

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

Quantity: 35,468 containers

Why Was This Recalled?

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

Where Was This Sold?

Distributed in Arkansas USA

About Rock Town Distillery, Inc.

Rock Town Distillery, Inc. has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report