CA BOTANA recalls Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol 5% due to CGMP deviations. Affected lots may pose quality risks.
CGMP Deviations
CA BOTANA is recalling Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol 5% because of manufacturing quality issues. This recall is for safety reasons related to potential product inconsistencies.
The product was made with CGMP (Current Good Manufacturing Practices) deviations, which means the manufacturing process did not meet quality standards. This could lead to inconsistent product quality, but the exact risk to consumers is not specified in the recall notice.
People who purchased the Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol 5% from CA BOTANA in the US. Those with the specific lot number D53081 are most at risk.
Check the product label for the lot number D53081 and expiration date 7/31/2026. The product is sold in 4.2 oz./120 g tubes under the brand Doctor D. Schwab Clinical Weh Weh.
Look for the lot number D53081 and expiration date 7/31/2026 on the tube.
The recall notice states there were CGMP deviations, but does not specify if the product is safe to use. Consumers should check the label for the lot number and expiration date.
The recall notice does not provide a remedy, so there is no specific action required beyond checking the label for the lot number D53081.
The recall notice does not mention any replacement or remedy options.
We’ve drafted a message you can send CA BOTANA to request your refund or repair — edit it as you like.
Subject: Recall D-0188-2026 — CA BOTANA CA BOTANA Hello, I own a CA BOTANA that is covered by recall D-0188-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
