Washington Homeopathic Products recalls specific tuberculinum bovinum liquid pellets (potency 12C, 30C, 200C) due to cGMP deviations. This recall affects certain lots sold in the US. Consumers should contact the manufacturer for details.
cGMP deviations
Washington Homeopathic Products is recalling specific tuberculinum bovinum liquid pellets (potency 12C, 30C, 200C) because of cGMP deviations. This means the product may not meet quality standards and could pose risks to consumers.
cGMP deviations refer to failures in manufacturing quality control processes. This could mean the product does not meet safety and quality standards, potentially leading to health risks. However, the exact nature of the deviation is not specified in the recall notice.
People who have purchased the specific tuberculinum bovinum liquid pellets (potency 12C, 30C, 200C) from Washington Homeopathic Products. Those using these products for medical purposes are most at risk.
Check for the product name 'Tuberculinum Bovinum', potency levels 12C, 30C, or 200C, and the lot numbers 19148 or 21028. The product is sold under Washington Homeopathic Products, Inc. in the US.
Reach out to Washington Homeopathic Products, Inc. at 260 JR Hawvermale Way, Berkeley Springs, WV 25411 for specific instructions on handling the recalled product.
Tuberculinum Bovinum liquid pellets with potency levels 12C, 30C, and 200C.
Lot numbers 19148 and 21028.
Check the product label for the potency levels 12C, 30C, or 200C and lot numbers 19148 or 21028.
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-1140-2022 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-1140-2022 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.
