Washington Homeopathic Products recalls Kali Sulphuricum 3X homeopathic medicine for manufacturing use only due to out-of-specification test results from HPTLC analysis.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling Kali Sulphuricum 3X homeopathic medicine for manufacturing use only because test results showed it did not meet specifications. This recall does not affect consumers using the product for personal health purposes.
The product failed identification testing using HPTLC analysis, meaning it does not meet the required specifications for homeopathic medicine. This could affect the accuracy of the product in manufacturing processes but poses no risk to end consumers.
Manufacturers and facilities using this homeopathic medicine for production purposes are affected. Consumers using this product for personal health are not at risk as it is intended for manufacturing only.
This product is labeled as 'Kali Sulphuricum 3X, 960ml 20% Alcohol, WHP Homeopathic Medicine, For Manufacturing Use Only'. The lot number 29475 expires on August 17, 2026.
Look for the label 'Kali Sulphuricum 3X, 960ml 20% Alcohol, WHP Homeopathic Medicine, For Manufacturing Use Only' and lot number 29475.
No, this product is intended for manufacturing use only and not for consumer health purposes.
Since the remedy is not specified in the recall, contact Washington Homeopathic Products directly for guidance.
The recall states out-of-specification test results, but no injury risk is mentioned for end users as it is for manufacturing use only.
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-0871-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0871-2021 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.
