CA Botana recalls Doctor D. Schwab Mineral Sunscreen SPF 50 with CGMP deviations. Affected units have NDC 35192-042-02 and Lot D54596. Stop using if you have this product.
CGMP Deviations
CA Botana is recalling its Doctor D. Schwab Mineral Sunscreen SPF 50 due to manufacturing deviations. This could affect product safety and quality. Consumers should check their product details to see if they are affected.
The product was manufactured with CGMP deviations, which are regulatory failures in the production process. This could lead to inconsistent product quality and potential safety risks. However, the specific nature of the deviations is not detailed in the recall notice.
People who own or use the Doctor D. Schwab Mineral Sunscreen SPF 50 with NDC 35192-042-02 and Lot D54596 are affected. Those using the product for extended periods may be at higher risk due to potential quality issues.
Check for the product name 'Doctor D. Schwab Mineral Sunscreen SPF 50', NDC code 35192-042-02, and Lot Code D54596. The product was manufactured in San Diego, CA and expires January 31, 2028.
Look for the NDC code 35192-042-02 and Lot Code D54596 on the product label.
The recall notice states there were CGMP deviations, but does not specify if the product is unsafe. Consumers should check their product details to see if they are affected.
The recall record does not provide a remedy, so there is no specific action required beyond checking product details.
Check for the NDC code 35192-042-02 and Lot Code D54596 on the product label. The product was manufactured in San Diego, CA and expires January 31, 2028.
We’ve drafted a message you can send CA Botana to request your refund or repair — edit it as you like.
Subject: Recall D-0183-2026 — CA Botana CA Botana Hello, I own a CA Botana that is covered by recall D-0183-2026 from CA Botana. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
