Class IIDrug
Menow Sunscreen Pressed Powder Spf35 Pa+++ recall
Summary
SHANTOU Qiwei industrial Co., Ltd is recalling MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++ (drug). According to the FDA report, the reason is: cGMP Deviations. The FDA rated this a Class II: the product may cause temporary or medically reversible health problems; serious harm is unlikely. Recall status: Ongoing.
Details from the FDA report
- Product
- 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
- Reason
- cGMP Deviations
- Lot / code info
- Lot #: 2024/10/11, Exp. Date 10/10/2027
- Quantity
- 2970 units
- Distribution
- CA only
- Recalling company
- SHANTOU Qiwei industrial Co., Ltd, Shantou, China
- Recall started
- August 8, 2026
- FDA report date
- September 30, 2026
- Classification
- Class II: The product may cause temporary or medically reversible health problems; serious harm is unlikely.
- Voluntary / mandated
- Voluntary: Firm initiated
- Status
- Ongoing
- Recall number
- D-0854-2026
What to do
- Check whether you have this product, and compare the lot numbers, codes, or dates on your package with the codes listed above.
- If it matches, stop using it and keep it away from children and pets.
- Contact the recalling company (SHANTOU Qiwei industrial Co., Ltd) or the store where you bought it about returns or refunds.
- Do not stop a prescribed medication without first talking to your pharmacist or doctor; they can help find a safe replacement.
- If you think the product made you or someone else sick, contact a doctor or pharmacist. In an emergency call 911.
- You can report problems to the FDA via MedWatch.