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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Topical Products

SG24 LLC: SkinGuard 24 Hand Sanitizers Recalled for Methanol Contamination

Agency Publication Date: September 1, 2020
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Summary

SG24 LLC is recalling approximately 151,700 units of SkinGuard 24 All-Day Hand Sanitizer products, including foam pump bottles, pocket pens, and individual towelettes. These products were found to contain 0.56% methanol, which is a toxic substance not permitted in hand sanitizers. The products were marketed without the required FDA approval, and consumers should immediately identify and stop using any affected items from their household.

Risk

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 accidentally ingest them and adolescents or adults who drink them as an alcohol substitute are at highest risk for methanol poisoning.

What You Should Do

  1. Check your hand sanitizer for the brand name 'SkinGuard 24' or 'Skin Guard 24' distributed by SG24 LLC, Bolingbroke, GA 31004.
  2. Identify if you have any of the following specific products: 2.67 oz foam pump bottles (UPC 793573147103, SKU 051220024), 8 oz foam pump bottles (UPC 793573147125, SKU 051230024), 10 mL Pocket Pens (UPC 793573147097, SKU 051210048), or individual 4"x6" Sanitizing Towelettes (SKU 03150025).
  3. Confirm that your product is part of the recall; all lots of these specific SKUs are affected as they are labeled to contain methanol.
  4. Stop using the recalled hand sanitizer immediately and do not dispose of it by pouring it down the drain or mixing it with other liquids.
  5. Contact your healthcare provider or pharmacist for guidance regarding potential exposure or health concerns.
  6. Return any unused product to the place of purchase for a refund and contact SG24 LLC for further instructions.
  7. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: SkinGuard 24 All-Day Hand Sanitizer (2.67 oz. bottle with foam pump)
Model:
SKU 051220024
Recall #: D-1571-2020
UPC Codes:
793573147103
Lot Numbers:
All lots labeled to contain methanol
Product: SkinGuard 24 All-Day Hand Sanitizer (8 oz. bottle with foam pump)
Model:
SKU 051230024
Recall #: D-1572-2020
UPC Codes:
793573147125
Lot Numbers:
All lots labeled to contain methanol
Product: Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen
Model:
SKU 051210048
Recall #: D-1573-2020
UPC Codes:
793573147097
Lot Numbers:
All lots labeled to contain methanol
Product: Skin Guard 24 All-Day Hand Sanitizing Towelette (1 4"x6" packet)
Model:
SKU 03150025
Recall #: D-1574-2020
Lot Numbers:
All lots labeled to contain methanol

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86270
Status: Resolved
Manufacturer: SG24 LLC
Manufactured In: United States
Units Affected: 4 products (9600 bottles; 9600 bottles; 10,000 pens; 122,500 individual wipe packets)
Distributed To: Nationwide
Agency Last Updated: September 12, 2020

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.