ROCK TOWN — Class II drug recall D-0715-2022
Terminated recall by Rock Town Distillery, Inc., reported 2022-03-30, distributed in AR. CGMP Deviations: FDA analysis found product to contain acetal and acetaldehyde above specification limits.
| Recall number | D-0715-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Rock Town Distillery, Inc., Little Rock, AR, United States |
| Recall initiated | 2022-03-10 |
| Classified | 2022-03-23 |
| Reported by FDA | 2022-03-30 |
| Terminated | 2023-08-23 |
| Distributed | AR |
| Quantity | 35,468 containers |
| Reason classes | cgmp |
| NDC | 74492-0002-01, 74492-0002-02, 74492-0002-03, 74492-0002-04 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0715-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.