Menow Sunscreen Pressed Powder SPF35 PA+++
MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++ has cGMP deviations.
Moderate risk
Taking it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
SHANTOU Qiwei industrial Co., Ltd, located in Shantou, China, recalled Menow Sunscreen Pressed Powder SPF35 PA+++, Net content, 9g/0.32 oz, because of cGMP Deviations. The company began the recall on August 8, 2026, and the FDA added it to the Enforcement Report on September 18, 2026. The product was distributed in California only, with 2970 units affected.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Affected if its lot code matches.
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
- 2024
Details
- Company began the recall
- Sold in
- Event ID
- 99625
- Recall No.
- D-0854-2026
- Company
- SHANTOU Qiwei industrial Co., LtdShantou, China
- Hazard
- Manufacturing deviation
- Quantity recalled
- 2970 units
- Recall type
- Voluntary: Firm initiated
- Customers told by
- Letter
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
