Valisa MFG LLC 2022-01-05 Health critical FDA
Health · FDA · Recall #FDA-D-0363-2022
kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles,… Recall
Issued January 5, 2022 · Valisa MFG LLC
In January 2022, Valisa MFG LLC recalled the kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles,…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug and contains methanol
What you should do
- 1 Stop using kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Valisa MFG LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Valisa MFG LLC
- Category
- Health
- Recall date
- January 5, 2022
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0363-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Valisa MFG LLC has 1 recall in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.