ZTE-1020 Homeopathic Formula Recalled for Failed Identification Testing
Washington Homeopathic Products, Inc. is recalling ZTE-1020 Formula (1000ml bottle, Lot #25740) distributed nationwide because identification testing based on HPTLC analysis produced out-of-specification results.
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: The FDA classified this as a Class II recall. The source text does not report any illnesses, injuries, or deaths. The hazard is testing non-compliance (out-of-specification identification results) rather than confirmed contamination or a documented risk of harm, making this a moderate-severity, precautionary recall.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling ZTE-1020 Formula, a 1000ml homeopathic medicine manufactured for Optimal Health Dimensions. The recall affects Lot #25740 (expiration date 8/17/2026) distributed nationwide in the USA.
The product is being recalled due to out-of-specification test results obtained during identification testing based on HPTLC (high-performance thin-layer chromatography) analysis. This means the product did not meet the required identification standards during testing.
Consumers who have purchased this product should contact Washington Homeopathic Products, Inc. or consult with their healthcare provider or pharmacist regarding appropriate next steps.
The recalled product
- Product
- ZTE-1020 Formula. Contents 1000ml. WHP Homeopathic Medicine, For Manufacturing Use Only, REMEDY: Aurum Metallicum 10X, Crataegus Oxyacantha 10X, Baryta Carbonica 10X, Digitalis Purpurea 10X, Zincum Muriaticum 13X, Chromium Sulphuricum 10X, Manganum Metallicum 10X, Dilution Alcoho
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- out-of-specification-testing
- identification-failure
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 # 25740
- Exp 8/17/2026
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- ModerateQuality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall
FDA (Drugs) · 2026-07-22
- ModerateLeader Carbamide Peroxide Earwax Removal Kit Recalled for Subpotency
FDA (Drugs) · 2026-07-22
- SevereCleviprex Injectable Emulsion Recall Due to Sterility Assurance Concerns
FDA (Drugs) · 2026-07-22
- ModerateFamily Wellness Carbamide Peroxide Earwax Removal Kit Subpotent Drug
FDA (Drugs) · 2026-07-22
- ModerateClinere Ear Wax Remover Recalled for Subpotent Carbamide Peroxide
FDA (Drugs) · 2026-07-22