Washington Homeopathic Products recalls ZTE-1034 Formula Antimicrobial Bowel (1000ml) due to out-of-specification test results from HPTLC analysis. This product 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 ZTE-1034 Formula Antimicrobial Bowel (1000ml) because test results showed it did not meet specifications. This product is intended for manufacturing use only and not for human consumption, so it poses no risk to consumers.
The product failed identification testing using HPTLC analysis, meaning it does not meet the required specifications. However, since it is labeled for manufacturing use only and not for human consumption, there is no risk to consumers.
This product is intended for manufacturing use only and not for human consumption. No consumers are affected as it was not meant to be used by end-users.
Check for the product name 'ZTE-1034 Formula Antimicrobial Bowel' with 1000ml capacity. It was manufactured by Washington Homeopathic Products, Inc. for Optimal Health Dimensions and has lot number 25887 with an expiration date of August 17, 2026.
Look for the product name 'ZTE-1034 Formula Antimicrobial Bowel' with 1000ml capacity and lot number 25887.
No, this product is labeled for manufacturing use only and not intended for human consumption.
The product failed identification testing based on HPTLC analysis, indicating it did not meet specifications.
Manufacturers and facilities that use this product for manufacturing purposes should check their records, as it is not intended for human consumption.
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-0885-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0885-2021 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.
