FDA
Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazol… Recalled: Lack of Assurance of Sterility
Lack of Assurance of Sterility
FDAClass II
MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++, Net content, 9g/0.32 oz, Manufactured by: Sha… Recalled: cGMP Deviations
MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++, Net content,… was recalled on August 8, 2026 in cooperation with the U.S. Food and Drug Administration because cGMP Deviations.
Is my unit affected?
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
Model, lot & date codes to check
Lot #: 2024/10/11, Exp. Date 10/10/2027
Units affected: 2970 units
Where it was sold: CA only
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
What's the hazard?
cGMP Deviations
Class II means the product might cause a temporary or medically reversible health problem; the chance of serious harm is remote.
Your remedy & how to claim it
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: SHANTOU Qiwei industrial Co., Ltd
Not sure what you're entitled to? Read our guide: what to do if your product is recalled.
Official recall notice
Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
View official notice →Related recalls
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