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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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Medium RiskFDA Drug
Medications & Supplements/Topical Products

Shane Erickson Inc: Hand Sanitizer Recalled for Subpotency and Possible Methanol Contamination

Agency Publication Date: January 22, 2021
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Summary

Shane Erickson Inc. is recalling 108,038 units of various IMC Wash-Free Hand Sanitizer products because they were manufactured in a facility where the FDA found products to be subpotent (lacking enough alcohol) and contaminated with methanol. Methanol, or wood alcohol, is a toxic substance that is not an acceptable ingredient for hand sanitizers and can be life-threatening if absorbed through the skin or ingested. These products were distributed nationwide in the USA and Canada in sizes ranging from 1.7 oz to 10.1 oz bottles, often featuring custom branding for organizations like SoFi Stadium, the Indiana Pacers, and Thrifty White Pharmacy.

Risk

Subpotent hand sanitizer fails to effectively kill germs, while methanol exposure can lead to nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death if ingested or absorbed through the skin.

What You Should Do

  1. Check your hand sanitizer bottles for the following identifying details: 1.7 fl. oz. bottles with UPC 8 19845 00597 8 and Lot 2020/05/11 (Exp 2023/05/10); 3.4 fl. oz. bottles with UPC 8 19845 00598 5 and Lot 20200510-3; or 10.1 fl. oz. bottles with UPC 8 19845 00599 2 and Lot 2020/05/11 (Exp 2023/05/10).
  2. Look for specific branding on the front labels including Sadie G. Mays Health & Rehabilitation Center, Pacers logo, northwood CHURCH, ROGERTHEROOFER.com, SoFi Stadium, SAFE-GUARD Products International, Safe-WAY JEVCO, TRACTION CAPITAL, United States Census 2020, or Thrifty White Pharmacy.
  3. Stop using these hand sanitizer products immediately if they match the recalled lot or UPC numbers.
  4. Contact your healthcare provider or pharmacist for guidance if you have experienced any adverse health effects after using these products.
  5. Return any unused product to the place of purchase for a refund and contact Shane Erickson Inc. for further instructions.
  6. Call the FDA Consumer Complaint hotline for additional questions at 1-888-723-3332 (1-888-SAFEFDA).

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: IMC Wash-Free Hand Sanitizer (1.7 fl. oz. / 50 ml)
UPC Codes:
819845005978
Lot Numbers:
2020/05/11 (exp 2023/05/10)
2020
Date Ranges: exp 2023/05/10
Product: IMC Wash-Free Hand Sanitizer (3.4 fl. oz. / 100 ml)
UPC Codes:
819845005985
Lot Numbers:
20200510-3
Date Ranges: MFG: 2020/05/10
Product: IMC Wash-Free Hand Sanitizer (10.1 fl. oz. / 300 ml)
UPC Codes:
819845005992
Lot Numbers:
2020/05/11 (exp 2023/05/10)
2020
Date Ranges: exp 2023/05/10

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87037
Status: Resolved
Manufacturer: Shane Erickson Inc
Sold By: Thrifty White Pharmacy; Sadie G. Mays Health & Rehabilitation Center; SoFi Stadium; United States Census 2020
Manufactured In: China
Units Affected: 3 products (36,505 bottles; 42,157 bottles; 29,376 bottles)
Distributed To: Nationwide

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.