QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui Cosmetics
Summary
The FDA issued a Class II for QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manu by HOYU(US) LOGISTICS INC. Reason: Subpotent.
Details
Source
Drug Recall
External ID
D-0643-2021
Action Date
2021-07-07
Status
Ongoing
Category
drug
Product Description
QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui Cosmetics Co., Ltd, Baiyun District, Guanzhou, China Distributed by HoYu (US) Logistics Inc UPC 6 926645 716288
Lot/Code Info: Lot # Q20200320, exp. date 03/19/2022
Quantity Affected: 30,880 bottles
Reason for Recall
Subpotent
Distribution
Product was destroyed nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-06-22
Company
Compton, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 19 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (HOYU(US) LOGISTICS INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does HOYU(US) LOGISTICS INC have FDA actions?
This is the only FDA action we have on record for HOYU(US) LOGISTICS INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0643-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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