Washington Homeopathic Products, Inc. is recalling approximately 15,452 glass amber bottles of 17 different homeopathic pellet products, including Pyrogenium, Influenzinum, and Candida Albicans. The recall was initiated due to manufacturing process deviations that violated federal quality standards (cGMP). The products were distributed nationwide in the United States. No incidents or injuries have been reported in connection with these products to date.
Deviations from manufacturing quality standards can result in products that do not meet required specifications for safety, purity, or potency. Using products manufactured under these conditions could potentially pose a health risk, though no adverse events have been confirmed.
You have 2 options:
Quantity: 109 glass amber bottles; Recall #: D-1135-2022
Quantity: 6,782 glass amber bottles; Recall #: D-1136-2022
Quantity: 5 glass amber bottles; Recall #: D-1137-2022
Quantity: 15 glass amber bottles; Recall #: D-1138-2022
Quantity: 15 glass amber bottles; Recall #: D-1139-2022
Quantity: 4 glass amber bottles; Recall #: D-1140-2022
Quantity: 2 glass amber bottles; Recall #: D-1141-2022
Quantity: 219 glass amber bottles; Recall #: D-1125-2022
Quantity: 5 glass amber bottles; Recall #: D-1126-2022
Quantity: 1,047 glass amber bottles; Recall #: D-1127-2022
Quantity: 134 glass amber bottles; Recall #: D-1128-2022
Quantity: 206 glass amber bottles; Recall #: D-1129-2022
Quantity: 7 glass amber bottles; Recall #: D-1130-2022
Quantity: 6,406 glass amber bottles; Recall #: D-1131-2022
Quantity: 49 glass amber bottles; Recall #: D-1132-2022
Quantity: 72 glass amber bottles; Recall #: D-1133-2022
Quantity: 375 glass amber bottles; Recall #: D-1134-2022
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.