Washington Homeopathic Products Althaea 6X Bladder Pills Recalled
Washington Homeopathic Products is recalling Althaea 6X Irritable Bladder Pills due to out-of-specification test results from identification testing. Ten bottles nationwide have been affected.
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 medicine involving out-of-specification test results from identity testing. No illnesses, injuries, or deaths are reported in the source text. The hazard is a quality/identity concern without evidence of patient harm.
Plain-English summary
Washington Homeopathic Products, Inc. is recalling Althaea 6X Irritable Bladder Sucrose/Lactose Pills, 1 OZ packaged bottles (Lot # 29377, expiration 8/17/2026), distributed nationwide in the USA.
The recall was issued because out-of-specification test results were obtained during identification testing using high-performance thin-layer chromatography (HPTLC) analysis. This indicates the product did not meet established specifications for identity verification.
Ten bottles of this product were distributed. Consumers who have purchased this product should discontinue use and contact the manufacturer or their healthcare provider with questions.
The recalled product
- Product
- Althaea 6X, Iritable Bladder* Sucrose/Lactose Pills, packaged as 1 OZ, WHP Homeopathic Medicine, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411.
- Manufacturer
- Washington Homeopathic Products, Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- identity-failure
- out-of-specification
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.
Related recalls
Same category
- ModerateLeader Carbamide Peroxide Earwax Removal Kit Recalled for Subpotency
FDA (Drugs) · 2026-07-22
- SevereCleviprex Injectable Emulsion Recall Due to Sterility Assurance Concerns
FDA (Drugs) · 2026-07-22
- ModerateClinere Ear Wax Remover Recalled for Subpotent Carbamide Peroxide
FDA (Drugs) · 2026-07-22
- ModerateFamily Wellness Carbamide Peroxide Earwax Removal Kit Subpotent Drug
FDA (Drugs) · 2026-07-22
- ModerateQuality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall
FDA (Drugs) · 2026-07-22