MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++, Net content, 9g/0.32 oz, Manufactured by: Shantzu Qiwei Industry Co. Ltd, A
Summary
The FDA issued a Class II for MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++, Net content, 9g/0.32 oz, Manufactur by SHANTOU Qiwei industrial Co., Ltd. Reason: cGMP Deviations.
Details
Source
Drug Recall
External ID
D-0854-2026
Action Date
2026-09-30
Status
Ongoing
Category
drug
Product Description
MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++, Net content, 9g/0.32 oz, Manufactured by: Shantzu Qiwei Industry Co. Ltd, Add: Quiwei Building, Yingloinguan, Xiashan, Chaonan district, Shantou City, Guangdong Province, China
Lot/Code Info: Lot #: 2024/10/11, Exp. Date 10/10/2027
Quantity Affected: 2970 units
Reason for Recall
cGMP Deviations
Distribution
CA only
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-08
Company
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 26 drug recalls issued in the same week, part of 66 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 (SHANTOU Qiwei industrial Co., Ltd) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SHANTOU Qiwei industrial Co., Ltd have FDA actions?
This is the only FDA action we have on record for SHANTOU Qiwei industrial Co., Ltd in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0854-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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