Washington Homeopathic Products, Inc. is recalling 5,678 bottles of various homeopathic medicines, including detox formulas, allergy drops, and remedies for symptoms like fear, bladder irritation, and bee stings. These products, sold nationwide through retailers like Peoples RX and Health Specialty, were recalled because laboratory testing could not confirm the identity of the ingredients as required. The recall affects a wide range of products in liquid, pill, and bulk forms manufactured between 2021 and 2026. No injuries or adverse reactions have been reported to date.
The medications failed 'out-of-specification' tests, meaning the manufacturer cannot confirm that the products contain the correct ingredients or potency levels. Using medications with unverified ingredients poses a risk to health, as consumers may not be receiving the expected treatment or could be exposed to unintended substances.
You have 2 options:
Recall #: D-0857-2021
Recall #: D-0858-2021
Recall #: D-0859-2021
Recall #: D-0860-2021
Recall #: D-0861-2021
Recall #: D-0862-2021
Recall #: D-0863-2021
Recall #: D-0864-2021
Recall #: D-0865-2021
Recall #: D-0866-2021
Recall #: D-0867-2021
Recall #: D-0868-2021
Recall #: D-0869-2021
Recall #: D-0870-2021
Recall #: D-0871-2021
Recall #: D-0872-2021 through D-0875-2021
Recall #: D-0876-2021
Recall #: D-0877-2021
Recall #: D-0878-2021
Recall #: D-0879-2021
Recall #: D-0880-2021
Recall #: D-0881-2021
Recall #: D-0882-2021
Recall #: D-0883-2021
Recall #: D-0884-2021
Recall #: D-0885-2021
Recall #: D-0886-2021
Recall #: D-0887-2021
Recall #: D-0888-2021
Recall #: D-0889-2021
Recall #: D-0890-2021
Recall #: D-0891-2021, D-0894-2021, D-0895-2021
Recall #: D-0892-2021, D-0893-2021
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.