Washington Homeopathic Products Haloderm Homeopathic Blend Recalled
Washington Homeopathic Products is recalling Haloderm Homeopathic Blend due to out-of-specification test results from 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 identified is a quality/testing specification issue rather than an acute safety threat, which aligns with the "Moderate" classification for quality-control concerns without demonstrated harm.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Haloderm Homeopathic Blend, For Manufacturing Use Only. The recall affects 3 liter bottles (Lot # 30308) distributed nationwide in the USA.
The product contains Dulcamara 10x, Nitricum Acidum 12x, Thuja Occidentalis 10x, Antimonium Crudum 12x, Calcarea Carbonica 12x, Silicea 12x, and 1.957 kg lactose in a 1,000 ml 20% alcohol solution. The manufacturer is Washington Homeopathic Products, Inc., located at 260 JR Hawvermale Way, Berkeley Springs, WV 25411, and the product is marketed by Health Specialty.
The recall was initiated due to out-of-specification test results obtained during identification testing based on HPTLC analysis. Consumers who have purchased this product should discontinue use and contact the manufacturer for instructions regarding return or disposal.
The recalled product
- Product
- Haloderm Homeopathic Blend, For Manufacturing Use Only, 1,000 ml 20% Alcohol, Contains: Dulcamara 10x, Nitricum Acidum 12x, Thuja Occidentalis 10x, Antimonium Crudum 12x, Calcarea Cadbonica 12x, Silicea 12x, WHP Homeopathic Medicine, FOr Manufacturing Use Only. 1.957 kg Lactose
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic
- Hazard
- specification-failure
- identification-testing-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 (1)
- Lot # 30308
Distribution
Distributed nationwide across the United States.
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