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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

CORGIOMED LLC: Leafree Instant Hand Sanitizer Recalled for Mislabeling as Edible Alcohol

Agency Publication Date: September 18, 2020
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Summary

Corgiomed LLC is recalling approximately 28,900 bottles of Leafree Instant Hand Sanitizer Aloe Vera because the product is incorrectly labeled as 'EDIBLE ALCOHOL.' This labeling suggests the product is safe for human consumption, but it is actually a topical hand sanitizer containing 70% ethyl alcohol that has not been approved as an oral drug. This product was distributed in North Carolina and Maryland in 100 mL, 300 mL, and 500 mL bottles. Consumers should immediately stop using this product and contact their healthcare provider if they have ingested it or experienced adverse reactions.

Risk

The product is misbranded and marketed as 'edible,' which poses a severe risk of alcohol poisoning or toxic ingestion if consumed as directed by the label. Ingesting high concentrations of ethyl alcohol intended for topical use can lead to central nervous system depression, vomiting, and other serious health complications.

What You Should Do

  1. Check your supply for Leafree Instant Hand Sanitizer Aloe Vera in 100 mL, 300 mL, or 500 mL bottles to see if the label contains the phrase 'EDIBLE ALCOHOL.'
  2. Verify if your product matches Lot # 2020A3010 with an expiration date of 05/30/2022.
  3. Match the UPC codes on the packaging: 6970495860325 (100 mL), 6970495860318 (300 mL), or 6970495860301 (500 mL).
  4. Stop using the product immediately and do not ingest it under any circumstances.
  5. Contact your healthcare provider or pharmacist for guidance regarding any health concerns or if the product was accidentally ingested.
  6. Return any unused product to the place of purchase for a refund and contact Corgiomed LLC for further instructions.
  7. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

๐Ÿ’ฐFull Refund

Contact healthcare provider and return product.

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

Affected Products

Product: Leafree Instant Hand Sanitizer Aloe Vera (100 mL)
UPC Codes:
6970495860325
Lot Numbers:
2020A3010 (Exp 05/30/2022)
Date Ranges: Expiration 05/30/2022
Product: Leafree Instant Hand Sanitizer Aloe Vera (300 mL)
UPC Codes:
6970495860318
Lot Numbers:
2020A3010 (Exp 05/30/2022)
Date Ranges: Expiration 05/30/2022
Product: Leafree Instant Hand Sanitizer Aloe Vera (500 mL)
UPC Codes:
6970495860301
Lot Numbers:
2020A3010 (Exp 05/30/2022)
Date Ranges: Expiration 05/30/2022

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86390
Status: Resolved
Manufacturer: CORGIOMED LLC
Manufactured In: China
Units Affected: 28900 bottles
Distributed To: North Carolina, Maryland

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.