CLASS II ONGOING Drug recall · Reported 7 Jul 2021 · FDA Enforcement Report

QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)) recalled

Hoyu(US) Logistics is recalling QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), distributed nationwide in the US. The recall was initiated on 22 Jun 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # Q20200320, exp. date 03/19/2022
Quantity recalled30,880 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0643-2021
FDA event ID
88140
Recalling firm
Hoyu(US) Logistics, Compton, CA
Classification
Class II
Status
Ongoing
Recall initiated
22 Jun 2021
FDA classified
29 Jun 2021
Reported
7 Jul 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay
Drug class
Hand Sanitizer

Timeline

22 Jun 2021Recall initiated by company
29 Jun 2021Classified by FDA+7 days
7 Jul 2021Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Subpotent

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

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

Where it was distributed

Product was destroyed nationwide.

Nationwide

Questions about this recall

Why was it recalled?

Subpotent

Which lots are affected?

Lot # Q20200320, exp. date 03/19/2022

Where was it sold?

Product was destroyed nationwide.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.