Z-103 GU DETOXING Homeopathic Medicine Recall for Failed Identification Testing
Washington Homeopathic Products is recalling Z-103 GU DETOXING, a 1000ml homeopathic medicine containing 20% alcohol, due to out-of-specification test results on identification testing using HPTLC analysis.
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 a Class II recall with no reported illnesses or injuries. The hazard is based on failed identification testing indicating a potential quality or identity issue, which constitutes a precautionary recall action.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Z-103 GU DETOXING, a homeopathic medicine product sold in 2/1 liter bottles with lot number 26364 and expiration date 8/17/2026. The product was distributed nationwide in the USA.
The recall was initiated because identification testing using HPTLC analysis produced out-of-specification results. This means the product did not meet the required standards for verification of its identity and composition.
Consumers and healthcare providers who have this product should contact Washington Homeopathic Products, Inc. for further instructions. The product is labeled "For Manufacturing Use Only" and "RX Only" and was manufactured for Optimal Health Dimensi by Washington Homeopathic Products located in Berkeley Springs, West Virginia.
The recalled product
- Product
- Z-103 GU DETOXING. Contents 1000ml 20% Alcohol. WHP Homeopathic Medicine. For Manufacturing Use Only, REMEDY: Agrimonia Eupatoria 24X, Alfalfa 24X, Althaea Officinalis 24X, Avena Sativa 24X, Boldo 24X, Carduus Marianus 24X, Chioanathus Virginica 24X, Cynara Scolymus 24X, Iria Ver
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- identification-testing-failure
- 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 # 26364
- Exp 8/17/2026
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- CriticalWarfarin Tablets Recalled After Mix-Up Between 2.5 mg and 5 mg Strengths
FDA (Drugs) · 2026-07-21
- ModerateFDA Recalls Pred Mild Ophthalmic Suspension Due to Failed Stability Specifications
FDA (Drugs) · 2026-06-03
- ModerateNicotine Transdermal System Patches Recalled for Oxidative Impurity Specification Failure
FDA (Drugs) · 2026-06-03
- ModerateGas-X Simethicone 125 mg softgels recall for incomplete labeling
FDA (Drugs) · 2026-05-27
- ModerateVitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid
FDA (Drugs) · 2026-05-27