ibspot is recalling three boxes of Taoscare Motion Sickness Patches because the product was marketed without the required FDA-approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). These patches, manufactured by Henan Xinyongtal Medical Technology, Ltd., were distributed in Wyoming and Virginia. Consumers should stop using these patches and consult a healthcare provider or pharmacist regarding any health concerns.
Using drugs that have not been reviewed by the FDA for safety and effectiveness poses a risk to consumers because the products have not met federal standards for quality, safety, or efficacy.
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Recall Number: D-0098-2026; Quantity: 3 boxes; Manufacturer: Henan Xinyongtal Medical Technology., Ltd.
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 ยท 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.