United States
Company name: SG24 LLCBrand name: SkinGuard24
Product recalled: All Day Hand Sanitizer
Reason of the recall: Contains Methanol
FDA Recall date: August 15, 2020
Recall details: SG24 LLC is voluntarily recalling the SkinGuard24 – All Day Hand Sanitizer products listed below to the consumer level. These products are being recalled because they are labeled to contain methanol.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, SG24 LLC. has not received any reports of adverse events related to the products of this recall.
Product Name: SkinGuard24 – All Day Hand Sanitizer Plastic bottle with Foam Pump
Size: 8 oz (250 mL)
UPC: 7 93573 147125
SKU: 051230024
Product Name: SkinGuard24 – All Day Hand Sanitizer Plastic bottle with Foam Pump
Size: 2.67 oz (70 ml)
UPC: 7 93573 147103
SKU: 051220024
Product Name: SkinGuard24 – All Day Hand Sanitizer Spray Pocket Pen
Size: 10 mL
UPC: 7 93573 14709
SKU: 051210048
Product Name: SkinGuard24 – All Day Hand Sanitizer Individual Towelette packaged as Single Use
Size: n/a
UPC: 2.5 x 3.75
SKU: 03150025
The recalled products are used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The recalled products are packaged in PET or High-density polyethylene (HDPE) plastic bottle or pen and as Individually packaged Towelettes with UPC’s 7935733144725, 79357314703, 7935733147103, 79357314709. The recalled products label colors are teal and blue which includes the words SkinGuard24- All Day Hand Sanitizer. The recalled products were distributed nationwide throughout the United States.
SG24 LLC is notifying its customers/distributors by recall letter and consumers via this press release. We are also notifying our distributors, who will help notify their customers by phone calls, emails, and/or mailed letters and is arranging for return of all Recalled Products.
Consumers, distributors, and retailers that have recalled products should stop use or distribution and return to place of purchase. Consumers should contact their physician or healthcare provider if they experience any of the aforementioned problems that may be related to the use of this product.
Check the full recall details on www.fda.gov
Source: FDA
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