Strophanthus hisp 30X Homeopathic Hives Pills Recalled for Testing Failures
Washington Homeopathic Products is recalling Strophanthus hisp 30X Hives pills after testing identified out-of-specification results in identification tests. The recall affects approximately 91 bottles 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 drug recall. The source identifies out-of-specification test results but does not report any illnesses, injuries, or hospitalizations, making it a precautionary recall. No hazard beyond the testing failure is explicitly described in the source.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Strophanthus hisp 30X, Hives Sucrose/Lactose Pills because out-of-specification test results were obtained during identification testing based on HPTLC (High-Performance Thin-Layer Chromatography) analysis.
The affected product was packaged in multiple sizes: 2 dram bottles (UPC 7 40640 47533 1), 4 dram bottles (UPC 7 40640 47537 9), 1 ounce bottles (UPC 7 40640 47541 6), and 2 ounce bottles (UPC 7 40640 47545 4). Approximately 91 bottles with Lot # 29061 were distributed nationwide in the USA.
Consumers who have purchased this product should not use it. Anyone with questions about this recall should contact Washington Homeopathic Products, Inc. at their Berkeley Springs, West Virginia facility.
The recalled product
- Product
- Strophanthus hisp 30X, Hives*, Sucrose/Lactose Pills , Packaged in (a) 2 dr, UPC 7 40640 47533 1; (b) 4 dr UPC 7 40640 47537 9; (c) 1 oz, UPC 7 40640 47541 6; (d) 2 oz, UPC 7 40640 47545 4; WHP Homeopathic Mecicine, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic
- Affected units
- 91
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 # 29061
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 · out of specification testing
See all →- ModerateQuebracho Homeopathic Pills Fail Identification Testing
FDA (Drugs) · 2021-10-06
- ModerateZTE-1034 Formula Antimicrobial Bowel homeopathic medicine recall
FDA (Drugs) · 2021-10-06
- ModerateHumulus 6X, 15X Homeopathic Pills Recalled for Failed Testing
FDA (Drugs) · 2021-10-06
- ModerateZTE-1020 Homeopathic Formula Recalled for Failed Identification Testing
FDA (Drugs) · 2021-10-06