Tinted moisturizer SPF 50 recalled over manufacturing practice deviations
CA Botana International is recalling 1,401 tubes of Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50 for CGMP deviations.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: Scored 2 because the record cites CGMP deviations without describing an identified defect or reported harm.
Plain-English summary
Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50, Zinc Oxide 21%, in 2.1 oz (61 g) tubes, NDC 35192-043-17, manufactured by CA Botana of San Diego, California, is being recalled for CGMP deviations.
The recall covers 1,401 tubes from lot D54757, expiring 31 March 2028. The product was distributed in California, Colorado, Florida, Puerto Rico and Washington. The FDA has classified the recall as Class II.
The enforcement record cites the manufacturing practice deviations without describing a specific defect or health consequence, and reports no injuries.
Anyone holding a tube from lot D54757 should follow the firm's instructions.
The recalled product
- Product
- Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50, Zinc Oxide 21%, 2.1 oz/61 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-043-17
- Manufacturer
- CA BOTANA International, Inc.
- Category
- Drug — Sunscreen
- Hazard
- Affected units
- 1,401
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 Code D54757
- exp 3/31/2028
Distribution
Part of a larger recall action
This product is one of 14 recalled by CA BOTANA International, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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