MENOW Sunscreen Powder Recalled for cGMP Deviations in California
Shantou Qiwei Industrial Co., Ltd is voluntarily recalling 2,970 units of MENOW Sunscreen Pressed Powder SPF35 PA+++ in California due to cGMP deviations.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The FDA classified this recall as Class II. According to the rubric, FDA Class II recalls without specific reports of hospitalization or significant injury are categorized as High severity.
Plain-English summary
Shantou Qiwei Industrial Co., Ltd is voluntarily recalling 2,970 units of MENOW Sunscreen Pressed Powder SPF35 PA+++ (9g/0.32 oz). The recall is limited to products distributed in California. The specific lot number is 2024/10/11, and the expiration date is 10/10/2027.
The recall was initiated by the firm on August 8, 2026, due to Current Good Manufacturing Practice (cGMP) deviations. The FDA has classified this recall as Class II, indicating that use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences.
Consumers who purchased this product in California should stop using it and follow the instructions provided by the recalling firm. The recall status is currently ongoing.
The recalled product
- 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
- Manufacturer
- SHANTOU Qiwei industrial Co., Ltd
- Category
- Drug — Sunscreen
- Hazard
- Affected units
- 2,970
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot #: 2024/10/11
- Exp. Date 10/10/2027
Distribution
Distributed in 1 state:
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