RecallRadar

FDA Drug recall D-0715-2022

ROCK TOWN - DISTILLERY - HAND SANITIZER, Alcohol Antiseptic 70%, Topical Solution packaged in a) 375 mL (12.7 fl. oz.), NDC 74492-0002-1

On 2022-03-30 the FDA classified a Class II recall of ROCK TOWN - DISTILLERY - HAND SANITIZER, Alcohol Antiseptic 70%, Topical Solution packaged in a) 375 mL (12.7 fl. oz.), NDC 74492-0002-1 by Rock Town Distillery, citing CGMP Deviations: FDA analysis found product to contain acetal and acetaldehyde above specification limits.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0715-2022
ClassificationClass II
Statusterminated
Initiated2022-03-10
Published2022-03-30
Last updated2026-09-13 11:52 UTC
CompanyRock Town Distillery
DistributionAR

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

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

Identifiers

code_infoNo lot number or expiration date.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0715-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.