Washington Homeopathic Products recalls ZTE-1035 Formula due to out-of-specification test results from HPTLC analysis. Affected units may pose safety risks.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling ZTE-1035 Formula, an antimicrobial combination product, because lab tests showed it did not meet quality standards. This could potentially lead to unsafe use of the product.
The product failed identification testing using HPTLC analysis, meaning it may not contain the correct ingredients as labeled. This could lead to ineffective or unsafe use of the product, though the risk is not severe.
Owners of ZTE-1035 Formula (1006 ml) with lot number 25697 are affected. People using homeopathic products for health purposes may be at risk if the product is not properly tested.
Check for the product name 'ZTE-1035 Formula, Antimicrobial Combination' with a 1006 ml size and lot number 25697. The product was manufactured by Washington Homeopathic Products in Berkeley Springs, WV.
Look for the lot number 25697 on the product label to confirm if it is affected.
The recall indicates the product failed quality tests, so it may not be safe. However, the risk level is low, and the product is not expected to cause serious harm.
Check the lot number on the product label. If it is 25697, contact Washington Homeopathic Products for further instructions.
The recall record does not specify a deadline for action.
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-0886-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0886-2021 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.
