June 2021 FDA Recall Drug by Hoyu(us) Logistics Inc
D-0643-2021 - Subpotent

This Class II drug recall was voluntarily initiated by Hoyu(us) Logistics Inc on June 22, 2021 for the product Drug. The FDA reported the reason for recall as subpotent. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0643-2021

Reason for Recall
Subpotent
Initiated
06-22-2021
Reported
07-07-2021
Quantity
30,880 bottles

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
88140
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Ongoing
Recalling Firm About Recalling Firm
The firm responsible for the recall.
HOYU(US) LOGISTICS INC
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Product was destroyed nationwide.
Product Description About Product Description
Full technical description of the product.
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

Batch or Lot Expiration Information

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