kleantouch HAND SANITIZER recall
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
Why was kleantouch HAND SANITIZER recalled?
Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug and contains methanol
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 1260-1, 1260-2, 1260-3, 1260-4. Exp. 04/2022
- Product
- 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
- Recalling firm
- Valisa MFG LLC
- Quantity
- 7704 bottles
- Distribution
- Nationwide in the USA
- Recall date
- January 5, 2022
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)