Washington Homeopathic Products recalls specific Vaccinotoxinum liquid pellets (Lot# 2512K) for cGMP deviations. This affects prescription-only homeopathic products sold in the US. No immediate action is required but consumers should check their product.
cGMP deviations
Washington Homeopathic Products is recalling specific Vaccinotoxinum liquid pellets (Lot# 2512K) because of cGMP deviations. This means the product may not meet quality standards for safe use, though the recall does not specify immediate health risks.
cGMP deviations refer to failures in manufacturing quality control processes. This could mean the product does not meet safety and purity standards, but the recall does not specify that this causes harm to users.
Prescription-only Vaccinotoxinum liquid pellets (Lot# 2512K) sold by Washington Homeopathic Products. People using these products for medical purposes are most at risk.
Check for the product name 'Vaccinotoxinum', potency levels (32X, 11C, 30C), and the lot number 2512K. This product was sold by Washington Homeopathic Products, Inc. in the US.
Identify if your product matches the description: Vaccinotoxinum liquid pellets with potency 32X, 11C, 30C, and lot number 2512K.
The recall states there were cGMP deviations, which could mean the product does not meet quality standards, but the official notice does not specify health risks.
The recall does not provide specific action steps beyond checking product details. No immediate action is required.
Check for the product name 'Vaccinotoxinum', potency levels (32X, 11C, 30C), and lot number 2512K on the label.
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-1141-2022 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-1141-2022 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.
