Data Foundry

Drug recalls 2022

Klean Touch Hand Sanitizer — Class I drug recall D-0298-2022

Terminated recall by Aroma Release Technologies Inc, reported 2022-01-05, distributed in NY, TX. Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug an

Recall numberD-0298-2022
Product typeDrug
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAroma Release Technologies Inc, Chattanooga, TN, United States
Recall initiated2021-11-30
Classified2021-12-28
Reported by FDA2022-01-05
Terminated2024-03-15
DistributedNY, TX
Reason classeschemical contamination, labeling, unapproved product
Lot numbers1620-1, 1620-3, 1620-4, 1820-4, 1820-5, 1920-1, 1920-2

Product

Klean Touch Hand Sanitizer (Ethyl Alcohol 70%) Ingredients Ethanol and Methanol, in 55-gallon drums, Aroma Release Technology, Inc., 7026 Discovery Drive, Chattanooga, TN 37416

Reason for recall

Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug and contains methanol

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-0298-2022. 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.