Washington Homeopathic Products recalls Viola od 6X and 30X homeopathic pills due to out-of-specification test results from HPTLC analysis. Affected products have specific UPCs and expiration dates.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling Viola od 6X and 30X homeopathic pills because lab tests showed they didn't meet quality standards. This could mean the pills aren't as intended, but the recall doesn't specify serious injury risks.
The pills failed quality tests based on HPTLC analysis, which checks for proper ingredient identification. This means the pills might not contain the correct active ingredients as labeled, potentially affecting their intended use.
Homeowners who purchased Viola od 6X or 30X pills with the listed UPCs and expiration dates are affected. People using these homeopathic remedies for bee stings or general health may be at risk if the pills don't meet quality standards.
Check for the product names Viola od 6X or 30X, Bee Stings, or Sucrose/Lactose Pills. Look for UPCs: 7 40640 50139 9, 7 40640 50141 2, or 7 40640 50149 8. The expiration date is August 17, 2026.
Verify the product name, UPC, and expiration date to confirm if it's affected.
The recall is due to out-of-specification test results from HPTLC analysis, meaning the pills didn't meet quality standards for ingredient identification.
The recall record doesn't specify a remedy, so check the product details to confirm if it's affected and contact the manufacturer if unsure.
The recall doesn't mention any safety risks or injuries, so this is a low-risk issue related to product quality.
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-0878-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0878-2021 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.
