Washington Homeopathic Products recalls ZTE 1015 Formula (1000ml) for manufacturing use only due to out-of-specification test results from HPTLC analysis. This product contains specific homeopathic dilutions.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling ZTE 1015 Formula (1000ml) for manufacturing use only because lab tests showed it didn't meet quality standards. This recall doesn't affect end consumers but is for internal quality control purposes.
The product failed quality tests using HPTLC analysis, meaning it doesn't meet the required specifications for homeopathic formulations. This is a quality control issue specific to manufacturing processes.
Manufacturers and facilities using this product for internal purposes. End consumers are not affected as this is for manufacturing use only.
Check for the product name 'ZTE 1015 Formula' with 1000ml capacity, manufactured for 'Optimal Health Dimensions', and lot number 25739. This product is intended for manufacturing use only, not for end consumers.
Verify the product is labeled for manufacturing use only with lot number 25739 and 1000ml capacity.
No, this product is specifically for manufacturing use only and not intended for end consumer use.
The product failed quality tests using HPTLC analysis, indicating it does not meet the required specifications for homeopathic formulations.
Since this is for manufacturing use only, end consumers are not affected. Manufacturers should follow their internal quality control procedures.
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-0888-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0888-2021 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.
