FOR IMMEDIATE RELEASE – Thornton, Colorado, Adam’s Polishes, LLC is voluntarily recalling lot 133475 of Adam’s Polishes Hand Sanitizer to the consumer level. FDA testing has found this lot to contain undeclared methanol. Adam’s Polishes is recalling 19 other lots in an abundance of caution.
Risk Statement: Persons who accidently ingest (drink) these products are at risk for methanol poisoning. Substantial methanol ingestion can result in coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. To date, Adam’s Polishes has not received any reports of injury, illness, or other adverse events related to this recall.
This product is used as a hand sanitizer marketed to help decrease bacteria on the skin when soap and water are not available. Adam’s Polishes Hand Sanitizer is packaged in 4oz., 8oz. 16oz., and one gallon bottles. These bottles are spray bottles for the 4oz, 8oz and 16oz and jugs for the gallon bottles. Please visit https://adamspolishes.com/pages/hs-voluntary-recallExternal Link Disclaimer, This is the Adam’s Polishes web site to check if your product’s lot number is included in this recall and, if so, how to request a credit. The hand sanitizer was distributed nationwide in the USA to internet customers between June 2020 and March 2022.
Adam’s Polishes is notifying its customers by email. Consumers who have any recalled Adam’s Polishes Hand Sanitizer products should immediately stop using the product and dispose of it in accordance with local regulations. Consumers can email Adam’s Polishes with a request for a credit at [email protected]. You will need to include a picture of the bottle including the lot number.
Consumers with questions regarding this recall can contact Adam’s Polishes at e-mail address [email protected] . Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.
Office hours and telephone number 9 am – 4pm mst 720-812-3460
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 recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
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As published on DailyDig.com