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Unrated Drug recall · FDA · Published June 3, 2020

Walker Emulsions Hand Sanitizer Recall: Unapproved Ethanol Risk

Walker Emulsions recalls 1-gallon hand sanitizer due to unapproved ethanol content. Consumers should check NDC 74940-0415-1 and lot #209638 for affected products.

🇺🇸 FDA recall #D-1416-2020DrugWalker Emulsions ›
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Contact the company

Recalling firmWALKER EMULSIONS INC4401 Se Johnson Creek Blvd · Portland, OR 97222-9218
✎ GovInfoNow plain-language explainer

Walker Emulsions is recalling 1-gallon hand sanitizer products because they contain ethanol that Health Canada says isn't approved for use in hand sanitizers. This could pose a safety risk if the product is used as intended. Read more at govinfonow.com/recall/37070-walker-emulsions-hand-sanitizer-recall-unapproved-ethanol-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/37070-walker-emulsions-hand-sanitizer-recall-unapproved-ethanol-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1416-2020

Cite this page

“Walker Emulsions Hand Sanitizer Recall: Unapproved Ethanol Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37070-walker-emulsions-hand-sanitizer-recall-unapproved-ethanol-risk. Based on FDA recall #D-1416-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1416-2020%22&limit=1).

The FDA announced on June 3, 2020, that Walker Emulsions Inc. is recalling its 60% alcohol hand sanitizer due to the use of an unapproved ethanol type. According to the FDA, the product contains DA-2I Ethanol, which is not approved for use in hand sanitizers.

How to tell if you have it

  • Brand: Walker Emulsions
  • Product: Walker Emulsions Hand Sanitizer (60%), Non-Sterile Solution, Alcohol Antiseptic 60%, 1 Gallon, Topical Solution
  • NDC: 74940-0415-1
  • Lot #: 209638

The hazard

The recall is classified as Class II because the hand sanitizer contains DA-2I Ethanol, a type of ethanol not approved for use in hand sanitizers. The FDA received notification of this issue from Health Canada.

Context

GovInfoNow's records show that Walker Emulsions has had other recent recalls of similar products, including the Zep Alcohol Sanitizer Spray Recall on May 22, 2026, and the Gasco Isopropyl Alcohol 70% Recall on May 29, 2026. Other recent recalls of similar products include the Haleon Gas-X Extra Strength Softgels Recall (June 4, 2026).

How to tell if you have this one

Check for the NDC code 74940-0415-1 and lot number 209638 on the product label. The product is sold by Walker Emulsions Inc. in Portland, Oregon.

  • Brand
    Walker Emulsions
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    US Distribution: Product distributed to sister plant site located in SC, and one donation made to consignee located in OR. Majority of hand sanitizer shipped to Canada (Health Canada has already received consignee information and classified the recall).
Recall numberProduct, codes & lots
D-1416-2020Walker Emulsions Hand Sanitizer (60%), Non-Sterile Solution, Alcohol Antiseptic 60%, 1 Gallon, Topical Solution, Walker Emulsions Inc., 4401 SE Johnson Creek Blvd., Portland, OR 97222, NDC 74940-0415-1; Lot # 209638
D-1417-2020Walker Hand Sanitizer, Non-Sterile Solution, Alcohol Antiseptic, 70%, 32 oz and 16 oz, Topical Solution, Walker Emulsions Inc., 4401 SE Johnson Creek Blvd., Portland, OR 97222, NDC 74940-0415-1; Lot # 210061
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for NDC 74940-0415-1 and lot #209638 on the product label.

Where it went and when

Where it was distributed

Distributed in Oregon and South Carolina, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “US Distribution: Product distributed to sister plant site located in SC, and one donation made to consignee located in OR. Majority of hand sanitizer shipped to Canada (Health Canada has already received consignee information and…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Oregon, South Carolina.

Recall timeline

FDA terminated this recall 3.9 years after the firm started it.

1. Firm started the recall: Jun 3, 202012. FDA classified it Class II: Jul 28, 202023. Published in FDA’s Enforcement Report: Jul 29, 202034. FDA terminated the recall: May 13, 2024420202024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-1416-2020 (June 3, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1416-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA