Washington Homeopathic Products recalls specific tuberculinum liquid pellets (potencies 1X-1M) due to cGMP deviations. This affects Rx-only products with lot numbers 20388 and 22728 sold in the US.
cGMP deviations
Washington Homeopathic Products is recalling certain tuberculinum liquid pellets (potencies 1X through 1M) because of manufacturing deviations that may affect quality. This recall applies to prescription-only products with specific lot numbers sold in the US.
The recall is due to cGMP (current Good Manufacturing Practice) deviations, which are regulatory standards ensuring product quality and safety. These deviations could potentially affect the product's safety or effectiveness, though the specific risk is not detailed in the recall notice.
Prescription holders of tuberculinum liquid pellets with lot numbers 20388 or 22728 are affected. Patients using these products for medical treatment are at risk if the manufacturing deviations impact safety.
Check the product label for lot numbers 20388 or 22728. The product is a prescription-only tuberculinum liquid pellet with specific potencies (1X, 12X, 24X, 30X, 1M).
Look for lot numbers 20388 or 22728 on the tuberculinum liquid pellets.
The recall is due to cGMP deviations, which are regulatory standards for product quality and safety. The specific impact on safety is not detailed in the notice.
The official recall notice does not specify a remedy or action steps beyond checking the product label for lot numbers 20388 or 22728.
The recall notice does not state whether the product is safe to use; it only mentions cGMP deviations.
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-1139-2022 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-1139-2022 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.
