Washington Homeopathic Products recalls Z-1020 Formula (1000ml 20% alcohol) for out-of-specification test results. This homeopathic medicine is for manufacturing use only and not intended for human consumption.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling Z-1020 Formula, a 1000ml homeopathic medicine with 20% alcohol, because lab tests showed it didn't meet quality standards. This product is only meant for manufacturing, not for human use, so it poses no risk to consumers.
The product failed quality tests for identification, meaning it may not contain the correct ingredients as labeled. However, because it's only for manufacturing use and not meant for human consumption, there's no risk to end users.
This recall affects manufacturers or facilities that use Z-1020 Formula for production. Consumers are not at risk since the product is not intended for human consumption.
Check for the Z-1020 Formula label with 1000ml 20% alcohol content. The product is manufactured by Washington Homeopathic Products, Inc. for use in manufacturing processes only.
Look for the Z-1020 Formula label with 1000ml 20% alcohol content and the manufacturer's address in Berkeley Springs, WV.
No, this product is specifically for manufacturing use only and not intended for human consumption.
The product failed identification tests based on HPTLC analysis, meaning it did not meet quality specifications.
Since it's for manufacturing use only, consumers do not need to take action. Only facilities using the product for production should verify their usage.
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-0882-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0882-2021 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.
