Washington Homeopathic Products recalls Occular Allergy Blend 87% Alcohol homeopathic medicine after out-of-specification test results from HPTLC analysis. No remedy specified in official notice.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling a homeopathic allergy blend product due to test results showing it doesn't meet specifications. This means the product may not be safe or effective as intended.
The product failed identification testing using HPTLC analysis, meaning it doesn't meet the required specifications. This could affect its safety or effectiveness, but the exact risk isn't clear from the notice.
People who purchased or use the Occular Allergy Blend 87% Alcohol homeopathic medicine from the manufacturer. Those with allergies or using the product for medical purposes may be at risk.
Check for the product name 'Occular Allergy Blend 87% Alcohol' with the lot number 30148. The product was manufactured by Washington Homeopathic Products in Berkeley Springs, WV.
Look for the product name and lot number 30148 on the label.
The official notice states the product failed identification testing, but doesn't specify if it's dangerous. The risk level is unknown.
The official notice doesn't specify a remedy, so no action is required beyond checking the product details.
Check for the product name 'Occular Allergy Blend 87% Alcohol' and lot number 30148 on the label.
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-0859-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0859-2021 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.
