Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Terminated Initiated Dec 6, 2021 (5 years ago)

kleantouch HAND SANITIZER

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

Cause type: Unapproved drug

The product was marketed without an approved NDA/ANDA, or does not meet the OTC monograph it claims to follow. Nothing about the product - dose, purity, safety - has been reviewed by FDA, so the claims on the box are unverified. All unapproved drug recalls.

What was recalled

kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles, Distributed by: Valisa MFG, LLC, Farmingdale, NY, 11735, Made in USA, UPC 6 86162 99246 1

Drug: Alcohol

Recalling firm
Valisa MFG LLC
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0363-2022 · FDA notice

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Alcohol recalls

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Other unapproved drug recalls from 2021

All unapproved drug recalls
Class I · High risk

Klean Touch Hand Sanitizer

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

Terminated Unapproved drug Aroma Release Technologies Inc D-0298-2022
Class II · Moderate risk

Cholestene capsules

Marketed Without an Approved NDA/ANDA

Terminated Unapproved drug High Performance Formulas, L.L.C. (HPF, L.L.C.) D-0727-2021