Taoscare Motion Sickness Patches 36-count box, Henan Xinyongtal Medical Technology., Ltd., Address: he nan sheng zhou ko
Summary
The FDA issued a Class II for Taoscare Motion Sickness Patches 36-count box, Henan Xinyongtal Medical Technolo by ibspot. Reason: Marketed Without an Approved NDA/ANDA.
Details
Source
Drug Recall
External ID
D-0098-2026
Action Date
2025-10-29
Status
Ongoing
Category
drug
Product Description
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
Lot/Code Info: none
Quantity Affected: 3 boxes
Reason for Recall
Marketed Without an Approved NDA/ANDA
Distribution
WY and VA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-09
Company
Elkins Park, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 58 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (ibspot) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ibspot have FDA actions?
This is the only FDA action we have on record for ibspot in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0098-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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