Washington Homeopathic Cinnamomum Pills Recalled for Failed Identity Testing
Washington Homeopathic Products is recalling Cinnamomum 6X and 30X homeopathic pills due to failed identification testing results. The products did not meet specifications in HPTLC analysis.
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 homeopathic products with failed identity testing. No illnesses, injuries, or deaths are reported in the source text. The hazard is a labeling/quality-specification issue rather than a direct safety threat, placing this in the Moderate category.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Cinnamomum 6X and Cinnamomum 30X homeopathic flatulence pills packaged in 4 Dram and 1 oz bottles. The recall affects lot #28626 with expiration date 8/17/2026, distributed nationwide in the USA.
The products are being recalled because identification testing based on HPTLC (High Performance Thin Layer Chromatography) analysis yielded out-of-specification results. The products did not meet required identity specifications.
Consumers who have purchased these products should discontinue use and contact Washington Homeopathic Products for further instructions.
The recalled product
- Product
- Cinnamomum 6X, Flatulence* Sucrose/Lactose Pills, Packaged as a) 4 Dram, b) 1 oz, and Cinnamomum 30X, Flatulence* Sucrose/Lactose Pills, Packaged as 4 Dram, WHP Homeopathic Medicine, Washington Homeopathic Products 260 JR Hawvermale Way, Berkeley Springs WV 25411
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic Medicine
- Affected units
- 6
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 # 28626
- 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 identity testing
See all →- ModerateAlthaea Officinalis Homeopathic Pills Recall Due to Failed Identity Testing
FDA (Drugs) · 2021-10-06
- ModerateAlthaea 6X Irritable Bladder Homeopathic Drops Recalled for Failed Identification Testing
FDA (Drugs) · 2021-10-06
- ModerateZ-1050 Formula Hepatodetox Homeopathic Medicine Fails Identification Testing
FDA (Drugs) · 2021-10-06
- ModerateViola od Homeopathic Medicine Recall for Failed Identity Testing
FDA (Drugs) · 2021-10-06
- ModerateZ-1070 Formula Anxioheal Homeopathic Medicine Recall for Testing
FDA (Drugs) · 2021-10-06