The FDA announced on December 6, 2021, that Valisa MFG LLC is recalling kleantouch HAND SANITIZER because the product contains methanol and is marketed without an approved New Drug Application. The agency classified the recall as Class I.
How to tell if you have it
- Brand: Valisa
- Product: kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles
- Distributed by: Valisa MFG, LLC
- UPC: 6 86162 99246 1
- Lot codes: 1260-1, 1260-2, 1260-3, 1260-4
- Expiration date: 04/2022
- Distribution: Nationwide in the USA
The hazard
The product is labeled to contain ethyl alcohol but contains methanol, making it an unapproved new drug. The FDA classified this as a Class I recall.
Context
GovInfoNow's records show other recent recalls of similar products include Zep Alcohol Sanitizer Spray Recall regarding microbial contamination risk on May 22, 2026, and OneSource Specialty Pharma Methohexital Sodium Recall concerning impurities risk serious injury on June 7, 2026. Fresenius Kabi Lidocaine HCl Injection Recall involving hair found in products occurred on July 16, 2026.