Taoscare recalled 3 boxes of motion sickness patches on October 9, 2025. The product was marketed without an approved NDA/ANDA. Consumers should stop using the patches immediately and seek guidance.
Marketed Without an Approved NDA/ANDA
Consumers and healthcare providers should stop using this product immediately. Contact ibspot or your healthcare provider for guidance. Notification method: E-Mail
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The recall involves Taoscare Motion Sickness Patches sold in 36-count boxes. The product was distributed in Wyoming and Virginia.
These patches were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). This raises concerns about their safety and efficacy.
There are no reported incidents associated with this product at this time. However, the lack of regulatory approval poses potential risks.
Stop using the Taoscare Motion Sickness Patches immediately. Contact ibspot or your healthcare provider for further guidance.
For more information, visit the FDA website or contact ibspot via email for assistance on the recall.
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