Washington Homeopathic Products recalls Althaea Officinalis 4X (Iritable Bladder) pills due to out-of-specification test results from HPTLC analysis. No remedy specified in the recall notice.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling Althaea Officinalis 4X (Iritable Bladder) pills because lab tests showed they didn't meet quality standards. This could mean the product isn't safe or effective as intended, but the recall doesn't specify a fix or replacement.
The product failed quality tests using HPTLC analysis, which checks for proper ingredient identification. This could mean the pills contain incorrect substances or are contaminated, but the recall doesn't specify how this affects safety or effectiveness.
People who own or use the Althaea Officinalis 4X pills with lot number 29377 (expiring 8/17/2026) are affected. Homeopathic users who take these pills may be at risk if the product isn't properly tested.
Check for the lot number 29377 on the packaging, which expires on 8/17/2026. The product is labeled as Althaea Officinalis 4X (Iritable Bladder) in sucrose/lactose pills.
Look for the lot number 29377 on the packaging to confirm if it's affected.
The recall notice does not specify any remedy or action to take.
The recall does not provide a remedy, so no specific action is required beyond checking the lot number.
The recall indicates the product failed quality tests, but it does not state if it's unsafe or ineffective.
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-0863-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0863-2021 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.
