Washington Homeopathic Products Kali Sulphuricum fails identification test
Washington Homeopathic Products is recalling Kali Sulphuricum 3X homeopathic medicine nationwide because identification testing using 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: This is an FDA Class II recall involving a homeopathic medicine with failed identification testing. No illnesses, injuries, or deaths are reported in the source text. The hazard is test-result-based rather than tied to documented harm, and homeopathic products present lower inherent risk than conventional pharmaceuticals, placing this in the Moderate category.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Kali Sulphuricum 3X, 960 mL bottles containing 20% alcohol (Lot #29475, expiration 8/17/2026), manufactured for use in further manufacturing. The product was distributed nationwide in the USA.
The recall was initiated because identification testing based on HPTLC (high-performance thin-layer chromatography) analysis produced out-of-specification test results. This means the product did not meet the required standards for identity verification through this analytical method.
Consumers and healthcare practitioners in possession of this product should discontinue use and contact Washington Homeopathic Products for instructions on return or destruction of affected bottles.
The recalled product
- Product
- Kali Sulphuricum 3X, 960ml 20% Alcohol, WHP Homeopathic Medicine, For Manufacturing Use Only. Manufactured by Washington Homeopathic Products 260JR hawvermale Way Berkeley Springs WV 25411.
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic Medicine
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 # 29475
- Exp 8/17/2026
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 39 recalled by Washington Homeopathic Products, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 39 products in this recall →Related recalls
Same manufacturer · Washington Homeopathic Products, Inc.
See all →- LowHomeopathic Kit Recalled for Label Mix-up Between Products
FDA (Drugs) · 2024-07-31
- ModerateHomeopathic Drug Recall: Vaccinotoxinum Products Due to Manufacturing Violations
FDA (Drugs) · 2022-06-22
- ModerateDrug recall: Tuberculinum Bovinum due to manufacturing practice deviations
FDA (Drugs) · 2022-06-22
- ModeratePyrogenium Homeopathic Remedy Recalled for Manufacturing Process Violations
FDA (Drugs) · 2022-06-22
- ModerateHomeopathic Colibacillinum Drug Recall Due to Manufacturing Deviations
FDA (Drugs) · 2022-06-22
Same hazard · failed identification testing
See all →- ModerateCedar Fever Drops Homeopathic Drug Recalled for Failed Identification Testing
FDA (Drugs) · 2021-10-06
- ModerateAconitum Napellus Fear Homeopathic Medicine Recalled for Failed Identification Testing
FDA (Drugs) · 2021-10-06
- ModerateWashington Homeopathic Cistus Canadensis pills fail quality identification testing
FDA (Drugs) · 2021-10-06
- ModerateYeast Guard Blend Homeopathic Medicine Fails Identification Testing
FDA (Drugs) · 2021-10-06
- ModerateAlthaea 30X Homeopathic Pills Recalled for Failed Identification Testing
FDA (Drugs) · 2021-10-06