Washington Homeopathic Products recalls Streptococcinum liquid pellets (potency 8C-200C) manufactured with cGMP deviations. This recall addresses potential quality issues in production.
cGMP deviations
Washington Homeopathic Products is recalling certain Streptococcinum liquid pellets (potency 8C, 9C, 30C, 200C) due to cGMP deviations in manufacturing. This recall is important because cGMP deviations can indicate quality issues that may affect product safety.
cGMP deviations refer to failures in the manufacturing process that may result in products not meeting quality standards. These deviations could potentially lead to unsafe products, though the specific risks are not detailed in this recall notice.
People who have purchased or received the recalled Streptococcinum liquid pellets (potency 8C, 9C, 30C, 200C) from Washington Homeopathic Products. Those using these products for medical purposes are most at risk.
Check for the product name 'Streptococcinum', potency levels 8C, 9C, 30C, or 200C, and the lot numbers 21902 or 21927. The product is sold by Washington Homeopathic Products, Inc. in the United States.
Identify the product name, potency levels, and lot numbers to confirm if your item is recalled.
The recall notice does not specify if the product is safe to use. cGMP deviations indicate potential quality issues, but the exact risks are not detailed.
The recall notice does not provide a remedy or action steps for affected products. You should check with the manufacturer for further instructions.
Check for the product name 'Streptococcinum', potency levels 8C, 9C, 30C, or 200C, and lot numbers 21902 or 21927. Contact Washington Homeopathic Products for confirmation.
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-1137-2022 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-1137-2022 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.
