Washington Homeopathic Products recalls ZTE-1020 Formula (1000ml) for out-of-specification test results from HPTLC analysis. This homeopathic medicine is for manufacturing use only and requires immediate action.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling ZTE-1020 Formula (1000ml) because lab tests showed it didn't meet quality standards. This homeopathic medicine is intended for manufacturing, not for human use, so it poses no risk to consumers.
The product failed quality tests for identification using HPTLC analysis. However, since it's designated for manufacturing use only, it does not pose a risk to end consumers.
This recall affects manufacturers or facilities that use ZTE-1020 Formula for production. Consumers are not at risk since this product is labeled for manufacturing use only.
Check for the ZTE-1020 Formula (1000ml) with lot number 25740, manufactured by Washington Homeopathic Products, Inc. in Berkeley Springs, WV. This product is intended for manufacturing use only.
Look for the ZTE-1020 Formula (1000ml) with lot number 25740, manufactured by Washington Homeopathic Products, Inc. in Berkeley Springs, WV.
No, this product is labeled for manufacturing use only and not intended for human consumption.
Since this product is for manufacturing use only, consumers are not affected. Contact the manufacturer if you are a facility using it for production.
The product failed quality tests for identification using HPTLC analysis, but it is not intended for human use.
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-0881-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0881-2021 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.
