Z-1070 Formula Anxioheal Homeopathic Medicine Recall for Testing
Washington Homeopathic Products, Inc. is recalling Z-1070 Formula Anxioheal, a 1000ml homeopathic remedy containing 20% alcohol, due to out-of-specification test results from HPTLC identification testing. The 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 with no reported illnesses or injuries. The hazard is based on out-of-specification test results that indicate a quality/identity control issue rather than a confirmed safety threat. No illness, injury, or fatality is documented in the source material.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Z-1070 Formula Anxioheal (lot #26007, expiration 8/17/2026) due to out-of-specification test results obtained during identification testing using HPTLC analysis.
Z-1070 Formula Anxioheal is a 1000ml homeopathic medicine containing 20% alcohol and various homeopathic ingredients including Causticum, Conium Maculatum, Crataegus Oxyacantha, and other botanical and mineral substances. The product is labeled "For Manufacturing Use Only" and "RX Only," and was manufactured for Optimal Health Dimensions by Washington Homeopathic Products, Inc. in Berkeley Springs, West Virginia.
The product was distributed nationwide in the USA. Consumers who have this product should follow directions from their healthcare provider regarding its use or discontinuation.
The recalled product
- Product
- Z-1070 Formula Anxioheal. Contents 1000ml 20% Alcohol. WHP Homeopathic Medicine, For Manufacturing Use Only, REMEDY:Causticum 30X, Conium Maculatum 8X, Conium Maculatum 12X, Crataegus Oxyacantha 12X, Crataegus Oxyacantha 30X, Ignatia Amara 24X, Lycopus Virginicus 12X, Phosphoricu
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- failed-identity-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 # 26007
- 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