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Lower risk Drug recall · FDA · Published June 9, 2021

World Source QiYu Hand Sanitizer Gel Recall: Subpotent Ethanol Risk

World Source recalls QiYu Hand Sanitizer Gel (500mL) due to subpotent ethanol content. This may not effectively sanitize hands. Affected units have specific lot numbers and expiration dates.

🇺🇸 FDA recall #D-0632-2021DrugWorld Source ›
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Recalling firmWorld Source Llc145 Oakwoods Dr · Wakefield, RI 02879-2512
✎ GovInfoNow plain-language explainer

World Source is recalling QiYu Hand Sanitizer Gel bottles that contain less effective ethanol. This means the sanitizer might not properly clean hands, potentially leaving germs behind. Consumers should check the lot number and expiration date to see if their product is affected. Read more at govinfonow.com/recall/36121-world-source-qiyu-hand-sanitizer-gel-recall-subpotent-ethanol-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/36121-world-source-qiyu-hand-sanitizer-gel-recall-subpotent-ethanol-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0632-2021

Cite this page

“World Source QiYu Hand Sanitizer Gel Recall: Subpotent Ethanol Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/36121-world-source-qiyu-hand-sanitizer-gel-recall-subpotent-ethanol-risk. Based on FDA recall #D-0632-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0632-2021%22&limit=1).

The FDA announced on June 9, 2021, that World Source LLC voluntarily recalled QiYu Hand Sanitizer Gel due to subpotency. The recall affects 6,300 bottles distributed to two New York hospitals.

How to tell if you have it

  • Brand: World Source
  • Product: QiYu Hand Sanitizer Gel
  • Manufacturer: Guangzhou Minghui Cosmetics Co., Ltd.
  • Lot code: 20200320
  • Expiration date: March 2022
  • Item #: TCM004

The hazard

The product is classified as subpotent. The FDA listed the recall classification as Class II.

Context

GovInfoNow's records show World Source has been involved in other recent recalls of similar products, including a Zep Alcohol Sanitizer Spray recall for microbial contamination risk on May 22, 2026, and a CoValence Laboratories Remedy Gel Hydrocortisone 1% recall for subpotent drug risk on March 18, 2026. Other recent recalls of similar products include a Gasco Isopropyl Alcohol 70% recall for subpotent drug risk on May 29, 2026.

How to tell if you have this one

Check for the product name 'QiYu Hand Sanitizer Gel', 500 mL bottles with a pump, and the lot number 20200320. The expiration date is March 2022. The manufacturer is Guangzhou Minghui Cosmetics Co., Ltd.

  • Brand
    World Source
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot number 20200320 and expiration date March 2022 on the bottle.

Where it went and when

Where it was distributed

Distributed in New York.

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: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: 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: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Product was distributed to two hospitals in NY.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New York.

Recall timeline

FDA terminated this recall 12 months after the firm started it.

1. Firm started the recall: Jun 9, 202112. FDA classified it Class II: Jun 16, 202123. Published in FDA’s Enforcement Report: Jun 23, 202134. FDA terminated the recall: Jun 9, 2022420212022
  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-0632-2021 (June 9, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0632-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 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