Washington Homeopathic Products recalls Althaea 30X, Iritable Bladder* Sucrose/Lactose Pills due to out-of-specification test results from HPTLC analysis. Affected lots include 29377 (expiring 8/17/2026).
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling Althaea 30X and Iritable Bladder* Sucrose/Lactose Pills because lab tests showed the product didn't meet quality standards. This could mean the pills aren't safe for use as intended.
The product failed quality tests using HPTLC analysis, which means the active ingredients might not be present in the correct amounts. This could lead to the pills not working as intended or causing unexpected reactions.
People who purchased the Althaea 30X pills from Washington Homeopathic Products in the US. Those with allergies to sucrose or lactose may be at higher risk.
Check for the lot number 29377 on the packaging. The product was sold by Washington Homeopathic Products, Inc. in Berkeley Springs, WV, and expires August 17, 2026.
Look for the lot number 29377 on the packaging to confirm if your product is affected.
The recall states the product failed quality tests, but the official notice doesn't specify if it's safe to use.
The recall record doesn't provide a remedy or action steps for affected products.
Check for the lot number 29377 on the packaging. The product was sold by Washington Homeopathic Products, Inc. in Berkeley Springs, WV, and expires August 17, 2026.
We’ve drafted a message you can send Washington Homeopathic Products to request your refund or repair — edit it as you like.
Subject: Recall D-0875-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0875-2021 from Washington Homeopathic Products. 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.
