Washington Homeopathic Products recalls ZTE-105 Gentle Detoxing formula due to out-of-specification test results from HPTLC analysis. This RX-only product was manufactured for optimal health but requires immediate attention.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling ZTE-105 Gentle Detoxing formula because lab tests showed it didn't meet quality standards. This is a prescription-only product that could be unsafe if used without proper testing.
The product failed quality tests using HPTLC analysis, which means it may not contain the correct ingredients or concentrations. This could lead to unsafe effects if used without proper medical supervision.
Prescription-only users of ZTE-105 Gentle Detoxing formula manufactured by Washington Homeopathic Products. Those who have the product with lot numbers 25950 or 26933 are most at risk.
Check for the product name 'ZTE-105 Formula Gentle Detoxing' with lot numbers 25950 or 26933. This prescription-only formula was manufactured by Washington Homeopathic Products in Berkeley Springs, WV.
Look for lot numbers 25950 or 26933 on the label to confirm if the product is affected.
The official recall states the product failed quality tests, so it is not safe to use as intended.
The recall does not specify a remedy, so contact Washington Homeopathic Products directly for guidance.
Check for lot numbers 25950 or 26933 on the label of ZTE-105 Formula Gentle Detoxing.
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-0858-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0858-2021 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.
