- Company Announcement Date:
- August 14, 2020
- FDA Publish Date:
- August 15, 2020
- Product Type:
- Reason for Announcement:
Recall Reason Description
- Company Name:
- SG24 LLC
- Brand Name:
- Product Description:
All Day Hand Sanitizer
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.
|SkinGuard24 – All Day Hand Sanitizer Plastic bottle with Foam Pump||8 oz (250 mL)||7 93573 147125||051230024|
|SkinGuard24 – All Day Hand Sanitizer Plastic bottle with Foam Pump||2.67 oz (70 ml)||7 93573 147103||051220024|
|SkinGuard24 – All Day Hand Sanitizer Spray Pocket Pen||10 mL||7 93573 14709||051210048|
|SkinGuard24 – All Day Hand Sanitizer Individual Towelette packaged as Single Use||2.5 x 3.75||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.
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
- Regular Mail or Fax: Download form 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.
Company Contact Information
P O Box 406
Bolingbroke, GA 31004