Lower riskDrug recall · FDA · Published July 12, 2021
Native Promotions QiYu Hand Sanitizer Recall: Subpotent Alcohol Content
Native Promotions recalls QiYu hand sanitizer bottles with 75% alcohol that may not be strong enough for effective hand cleaning. Consumers should check product details and contact the company for guidance.
“Native Promotions QiYu Hand Sanitizer Recall: Subpotent Alcohol Content.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/36096-native-promotions-qiyu-hand-sanitizer-recall-subpotent-alcohol-content. Based on FDA recall #D-0793-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0793-2021%22&limit=1).
Native Promotions, Inc. recalled QiYu Hand Sanitizer bottles due to subpotent drug risks, the FDA said on July 12, 2021. The voluntary Class II recall affects 4,320 units distributed to tribal nations.
How to tell if you have it
Brand: Native Promotions
Product: QiYu Hand Sanitizer (ethyl alcohol 75% (v/v))
The FDA classified the QiYu Hand Sanitizer as subpotent. The agency announced the recall on July 12, 2021.
Context
GovInfoNow's records show other recent recalls of similar products include Gasco Isopropyl Alcohol 70% Recall (2026-05-29), Gasco Industrial Isopropyl Alcohol 70% Recall (2026-05-29), and Zep Alcohol Sanitizer Spray Recall (2026-05-22).
How to tell if you have this one
Check for the product name 'QiYu Hand Sanitizer', 16.9 fl oz (500 ml) bottles, and the batch number Q20200510. The product was manufactured by Guangzhou Minghui Cosmetics Co., Ltd in China and distributed by Native Promotions.
Brand
Native Promotions
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the batch number Q20200510 and NDC 74447-010 on the product label.
Where it went and when
Where it was distributed
Distributed in 13 states.
Listed by the agency
Not listed
FDA distribution: “Tribal nations in the following states: NC, MS, NY, FL, AL, SC, ME, CT, MA, VA, TX, LA, RI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Connecticut, Florida, Louisiana, Maine, Massachusetts, Mississippi, New York, North Carolina, Rhode Island, South Carolina, Texas, Virginia.
Recall timeline
FDA terminated this recall 2.2 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0793-2021 (July 12, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0793-2021 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.