SHANTOU Qiwei industrial recall: Menow Sunscreen Pressed Powder SPF35 Pa+++
SHANTOU Qiwei industrial Co., Ltd is recalling Menow Sunscreen Pressed Powder SPF35 Pa+++ because of manufacturing-practice violations – 2970 units. The U.S. Food and Drug Administration published the recall on September 30, 2026; it began on August 8, 2026. Distributed in 1 state (California).
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Menow Sunscreen Pressed Powder SPF35 Pa+++ |
| Brand | SHANTOU Qiwei industrial |
| Company | SHANTOU Qiwei industrial Co., Ltd |
| Type | Drugs |
| Classification | Class II |
| Recall date | August 8, 2026 |
| Published by FDA | September 30, 2026 |
| Quantity | 2970 units |
| Recall ID | 99625 |
Recalled products
- 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
- FDA recall number
- D-0854-2026
- Codes, lots and dates
- Lot #: 2024/10/11, Exp. Date 10/10/2027
- Quantity
- 2970 units
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99625
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Shantou, China
Why it was recalled
The problem: manufacturing-practice violations.
The reason the FDA lists: “cGMP Deviations”
Where it was sold
1 state: California. Distribution as the FDA records it: “CA only”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99625, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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About this recall
Is SHANTOU Qiwei industrial Menow Sunscreen Pressed Powder SPF35 Pa+++ recalled?
Yes. SHANTOU Qiwei industrial Co., Ltd recalled it on August 8, 2026; FDA published it September 30, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Because of manufacturing-practice violations. The reason given: cGMP Deviations
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
In 1 state (California).
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.