Washington Homeopathic Products recalls specific Candida Albicans liquid pellets with potency levels 9C-288X due to cGMP deviations. Consumers should check lot numbers 17759, 18479, 18133 for affected products.
cGMP deviations
Washington Homeopathic Products is recalling Candida Albicans liquid pellets with specific potency levels because of manufacturing deviations. This recall affects consumers who purchased these products with the listed lot numbers, as the products may not meet quality standards.
The recall is due to cGMP deviations, which means the products may not meet current Good Manufacturing Practices. This could affect the product's quality and safety, but the specific risks are not clearly described in the recall notice.
Anyone who purchased Candida Albicans liquid pellets with potency levels 9C-288X from Washington Homeopathic Products. People using these products for homeopathic treatment are most at risk due to potential quality issues.
Check the product label for potency levels 9C-288X and lot numbers 17759, 18479, or 18133. These products were sold by Washington Homeopathic Products in Berkeley Springs, WV.
Look for potency levels 9C-288X and lot numbers 17759, 18479, or 18133 on the product label.
The recall is due to cGMP deviations, which means the products may not meet quality standards.
Lot numbers 17759, 18479, and 18133 are affected.
The recall notice does not specify a stop-use instruction, so you do not need to stop using them immediately.
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-1127-2022 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-1127-2022 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.
