Washington Homeopathic Products recalls Syphilinum liquid pellets (potencies 9C, 30C, 200C, 10X, 12X) with lot numbers 20389-20441 due to cGMP deviations in manufacturing.
cGMP deviations
Washington Homeopathic Products is recalling certain Syphilinum liquid pellets (potencies 9C, 30C, 200C, 10X, 12X) because of cGMP manufacturing deviations. This recall affects people who have these specific lot numbers and may pose a risk to product safety.
cGMP deviations refer to failures in the manufacturing process that could affect product quality and safety. These deviations may result in unsafe levels of active ingredients or contaminants in the liquid pellets.
People with Syphilinum liquid pellets (potencies 9C, 30C, 200C, 10X, 12X) from Washington Homeopathic Products with lot numbers 20389, 20390, or 20441 are affected. Those using these products for medical purposes may be at risk due to manufacturing issues.
Check the product label for Syphilinum liquid pellets with potencies 9C, 30C, 200C, 10X, or 12X. Look for lot numbers 20389, 20390, or 20441 on the packaging.
Look for lot numbers 20389, 20390, or 20441 on the Syphilinum liquid pellets packaging.
Syphilinum liquid pellets with potencies 9C, 30C, 200C, 10X, and 12X from Washington Homeopathic Products with lot numbers 20389, 20390, or 20441.
The recall is due to cGMP deviations in manufacturing, which could affect product safety and quality.
The recall record does not specify a remedy, so contact Washington Homeopathic Products directly for guidance.
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-1138-2022 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-1138-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
