Althaea 6X Irritable Bladder Homeopathic Drops Recalled for Failed Identification Testing
Washington Homeopathic Products is recalling Althaea 6X Irritable Bladder drops (Lot #29377) distributed nationwide because identification testing via 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 for a homeopathic drug product with out-of-specification test results. No illness, injury, or confirmed harm is reported in the source text. The hazard is quality-control based rather than evidence of actual contamination or mislabeling, making this a precautionary quality issue.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Althaea 6X, Irritable Bladder 20% Alcohol Drops, packaged as 15 ml bottles. The recall affects Lot #29377, which is scheduled to expire on August 17, 2026.
The product was recalled due to out-of-specification test results obtained during identification testing based on HPTLC (High-Performance Thin-Layer Chromatography) analysis.
The product was distributed nationwide in the United States. Consumers who have purchased this product should discontinue use and consult with their healthcare provider if they have questions or concerns.
The recalled product
- Product
- Althaea 6X, Iritable Bladder* 20% Alcohol, Drops, packaged as 15 ml, WHP Homeopathic Medicine, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411.
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic
- Affected units
- 10
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 # 29377
- 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.
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