Motion Sickness Patches Recall: Taoscare 36-count box
Announced 2025-10-29 · FDA
Taoscare Motion Sickness Patches 36-count boxes marketed by ibspot were marketed without an approved NDA/ANDA, according to the FDA. The recall involves 3 boxes distributed in Wyoming and Virginia. No recall number is provided, and no corrective-action details are available.
| Brand | ibspot |
|---|---|
| Product | Taoscare Motion Sickness Patches 36-count box, Henan Xinyongtal Medical Technology., Ltd., Address: he nan sheng zhou kou shi huai yang xian gong ye yuan qu, X003SR097N |
| Reason | Marketed Without an Approved NDA/ANDA |
| Severity | moderate |
| Units affected | 3 |
| Distribution | WY and VA |
| Agency | FDA |
| Recall / campaign no. | none |
WHAT YOU SHOULD DO
- Stop using the recalled patches immediately.
- If you have the Taoscare 36-count box distributed to WY or VA, set it aside and contact the seller for disposal or a refund.
- Check for updates from the FDA or the retailer for instructions about return or disposal.
- If you have any adverse health effects, consult a healthcare professional.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.