artnaturals® Issues Voluntary Recall of Limited Batches of 8oz Bottles of Scent Free Hand Sanitizer Due to Presence of Impurities
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Recall Reason DescriptionDue to Presence of Impurities
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Product DescriptionScent Free Hand Sanitizer
UPDATE TO NOTICE – Los Angeles, CA, November 3, 2021
FOR IMMEDIATE RELEASE – Los Angeles, CA, Oct 26, 2021
artnaturals is voluntarily recalling several manufacturing lots of artnaturals 8oz Scent Free Hand Sanitizer. FDA testing identified 8oz bottles of Scent Free Hand Sanitizer from a single manufacturing lot: G20128A, contained several impurities. Upon being contacted by the FDA, artnaturals responded immediately to proactively address the matter out of an abundance of caution. After multiple communications with the FDA, the two groups have mutually agreed that artnaturals will issue a voluntary recall of several additional manufacturing lots of 8oz Scent Free Hand Sanitizer.
Exposure to the impurities found can happen naturally in our surrounding environments through inhalation, oral consumption and/or skin absorption. Long term exposure could result in cancers-including leukemia, cancer of the bone marrow and blood disorders. To date, artnaturals has not received any reports of adverse events related to this voluntarily recalled product.
The product is used to remove germs on hands that may cause illness when soap and water are not available and is packaged in 8 oz clear bottles. The voluntarily recalled manufacturing lots of artnaturals 8oz bottles of SCENT FREE hand sanitizer are as follows:
|MFG DATE||MFG BATCH #||MFG LOT #||EXPIRE DATE||UPC #|
The product can be identified by the pictures below.
Products purchased at Walmart, Target, Costco, RiteAid, Publix, HEB, Menards, Amazon and most other retailers were not affected. artnaturals has notified the affected retailer by letter and arranged a return of all affected products. Consumers that currently have this voluntarily recalled product should stop using and appropriately discard it.
Consumers may contact artnaturals Customer Experience with questions or to request a refund by calling 1-855-278-4488 Mon-Fri, 8am-5pm Pacific Time. Consumers should contact their physician or healthcare provider if they have any questions or concerns related to using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
- Complete and submit the report Online: www.fda.gov/medwatch/report.htm
- Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This voluntary recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Company Contact Information
- Michael Bowers