Washington Homeopathic Products recalls Althaea 6X and Iritable Bladder 20% Alcohol Drops 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 6X and Iritable Bladder 20% Alcohol Drops because lab tests showed they didn't meet quality standards. This means the product might not be safe or effective as intended.
The product failed quality tests using HPTLC analysis, which is a method to check if homeopathic medicines meet specifications. This could mean the product isn't safe or effective as labeled, but the exact risk isn't clear from the recall notice.
People who own or use the Althaea 6X or Iritable Bladder 20% Alcohol Drops from Washington Homeopathic Products are affected. Those who have the specific lot number 29377 (expiring 8/17/2026) are most at risk.
Check for the product name 'Althaea 6X' or 'Iritable Bladder* 20% Alcohol Drops', packaged in 15 ml bottles. The lot number 29377 (expiring 8/17/2026) is the affected batch.
Look for the product name and lot number on the bottle to confirm if it's affected.
The recall states the product failed quality tests, but the exact risk isn't specified. The official notice doesn't say if it could cause harm.
The recall doesn't provide a remedy, so there's no action required beyond checking if you have the affected lot.
Check the product label for the lot number 29377 (expiring 8/17/2026) to see if it matches the recalled batch.
We’ve drafted a message you can send Washington Homeopathic to request your refund or repair — edit it as you like.
Subject: Recall D-0874-2021 — Washington Homeopathic Washington Homeopathic Hello, I own a Washington Homeopathic that is covered by recall D-0874-2021 from Washington Homeopathic. 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.
