Washington Homeopathic Products recalls Althaea 6X and Iritable Bladder pills due to out-of-specification test results from HPTLC analysis. Consumers should contact the company for details.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling Althaea 6X and Iritable Bladder pills because lab tests showed they didn't meet quality standards. This could mean the pills aren't safe or effective as intended.
The pills failed quality tests using HPTLC analysis, which checks for proper ingredient levels. This could mean the pills don't work correctly or could be unsafe for some people.
People who bought these pills from Washington Homeopathic Products in the U.S. are affected. Those with allergies to sucrose or lactose may be at higher risk.
Check for the 1 OZ packaging with lot number 29377, which expires on August 17, 2026. The product is sold by Washington Homeopathic Products in Berkeley Springs, West Virginia.
Reach out to Washington Homeopathic Products at 260 JR Hawvermale Way, Berkeley Springs, WV 25411 for details on the recall.
The product failed quality tests using HPTLC analysis, meaning it didn't meet the required specifications for identification testing.
Contact Washington Homeopathic Products directly for instructions on what to do with the recalled pills.
The recall is due to quality issues, not a specific safety hazard like injury or illness. The official notice does not mention risks of injury.
We’ve drafted a message you can send Washington Homeopathic to request your refund or repair — edit it as you like.
Subject: Recall D-0873-2021 — Washington Homeopathic Washington Homeopathic Hello, I own a Washington Homeopathic that is covered by recall D-0873-2021 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.
