Washington Homeopathic Products recalls Cedar Fever Drops (30mL) due to out-of-specification test results from HPTLC analysis. Consumers should contact the manufacturer for details.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Washington Homeopathic Products is recalling Cedar Fever Drops (20% USP ALCO: 30mL) because lab tests showed the product did not meet quality standards. This could mean the product is unsafe for use.
The product failed quality tests for identification using HPTLC analysis. This suggests the product may not contain the correct ingredients or could be contaminated, but the specific risk to health is not clearly stated in the recall notice.
People who purchased Cedar Fever Drops from retailers in the US, particularly those using homeopathic remedies for allergies. Those with allergies may be at higher risk.
Check for the product name 'Cedar Fever Drops', 20% USP ALCOHOL, 30 mL, manufactured for Peoples RX. Look for UPC 7 40640 64166 8 or lot numbers 25586 or 27410.
Reach out to Washington Homeopathic Products at 3801 S Lamar, Austin, TX 78704 for specific instructions on handling the product.
The recall states the product failed quality tests, but does not specify the exact health risk. The official notice does not state if the product could cause injury or illness.
Check for the product name 'Cedar Fever Drops', 20% USP ALCOHOL, 30 mL, manufactured for Peoples RX. Look for UPC 7 40640 64166 8 or lot numbers 25586 or 27410.
The recall does not specify a remedy, so contact Washington Homeopathic Products for instructions.
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-0862-2021 — Washington Homeopathic Products Washington Homeopathic Products Hello, I own a Washington Homeopathic Products that is covered by recall D-0862-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
