Cedar Fever Drops Homeopathic Drug Recalled for Failed Identification Testing
Washington Homeopathic Products is recalling Cedar Fever Drops due to out-of-specification test results from identification testing. The affected product was distributed nationwide.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II recall for a homeopathic drug product with out-of-specification test results from identification testing. No illnesses, injuries, or deaths are reported in the source text. The hazard is a testing/quality control failure without reported harm, which falls under the Moderate category for non-critical quality issues.
Plain-English summary
Cedar Fever Drops, a 30 mL homeopathic drug product containing 20% USP alcohol and manufactured for Peoples RX, is being recalled by Washington Homeopathic Products, Inc. The recall affects approximately 1,931 bottles identified by Lot Numbers 25586 and 27410.
The product is being recalled because out-of-specification test results were obtained during identification testing using HPTLC (High-Performance Thin-Layer Chromatography) analysis. This means the product failed to meet required testing specifications for product identification.
The product was distributed nationwide in the USA. Consumers who have purchased Cedar Fever Drops with the affected lot numbers should stop use and contact their retailer or the manufacturer for further instructions.
The recalled product
- Product
- Cedar Fever Drops, 20% USP ALCOHOL, 30 mL, homeopathic drug for symptoms of cder allerges, Manufactured for Peoples RX, 3801 S Lamar, Austin, TX 78704. UPC 7 40640 64166 8
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic
- Hazard
- failed-identification-testing
- out-of-specification
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot # 25586
- 27410
Distribution
Distributed nationwide across the United States.
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