Washington Homeopathic Products recalls specific Candida Parapsilosis liquid pellets with potency levels 14X-30X due to cGMP deviations. Consumers should check lot numbers on the product label for affected items.
cGMP deviations
Washington Homeopathic Products is recalling certain Candida Parapsilosis liquid pellets that were made with potency levels from 14X to 30X. The recall is due to manufacturing deviations that may affect product safety.
The product was made with cGMP (current Good Manufacturing Practices) deviations, which means the production process did not meet safety and quality standards. This could potentially lead to unsafe levels of ingredients in the product, though the exact risk is not specified in the recall notice.
Anyone who purchased the specific potency levels of Candida Parapsilosis liquid pellets from Washington Homeopathic Products. People using homeopathic remedies for candida or similar conditions may be at risk.
Check the product label for potency levels 14X, 15X, 16X, 20X, 28X, 30X, 9C, 10C, 13C, 15C, 25C, 30C, 13X, 27X, 30X. The lot numbers 22315 or 26502 are also associated with this recall.
Look for potency levels 14X through 30X on the label to identify affected items.
The product was made with cGMP deviations, which means the manufacturing process did not meet safety and quality standards.
The recall notice does not specify a remedy or action for affected products.
Check the product label for potency levels 14X, 15X, 16X, 20X, 28X, 30X, 9C, 10C, 13C, 15C, 25C, 30C, 13X, 27X, 30X and lot numbers 22315 or 26502.
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-1128-2022 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-1128-2022 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.
