HIGH

ibspot Taoscare Motion Sickness Patches Recalled Over NDA/ANDA Issue (2025)

ibspot recalled Taoscare Motion Sickness Patches, 36-count boxes, sold in Wyoming and Virginia. The recall centers on marketing without an approved NDA or ANDA. Consumers and healthcare providers should stop using the product immediately and contact ibspot for guidance.

Quick Facts at a Glance

Recall Date
October 9, 2025
Hazard Level
HIGH
Brand
ibspot
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
2 states
At-Risk Groups
GENERAL

Hazard Information

Marketed Without an Approved NDA/ANDA

What You Should Do

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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About This Product

Taoscare Motion Sickness Patches are a transdermal patch product marketed under the ibspot brand. They are sold in 36-count boxes and intended to provide relief from motion sickness.

Why This Is Dangerous

The defect is regulatory in nature. The product was marketed without an approved NDA/ANDA. This constitutes noncompliance with drug approval requirements rather than a physical defect in the patch.

Industry Context

This recall is not described as part of a broader industry pattern by the agency.

Real-World Impact

Consumers face potential regulatory risk and confusion about product status. Financial loss may occur if refunds or replacements are offered. No injuries have been reported to date.

Practical Guidance

How to identify if yours is affected

  1. Locate Taoscare Motion Sickness Patches, 36-count box bearing the ibspot brand.
  2. Check for the absence of an approved NDA/ANDA labeling note on packaging.
  3. Note WY and VA distribution as part of the recall footprint.

Where to find product info

Refer to the FDA enforcement recall page linked in the notice for official guidance and status.

What timeline to expect

Refunds or replacements, if offered, typically take several weeks to process after confirmation of eligibility.

If the manufacturer is unresponsive

  • Escalate to ibspot via recall notification email
  • If still unresponsive, contact FDA/FTC consumer hotlines or file a complaint with CPSC if applicable
  • Keep records of all communications and packaging.

How to prevent similar issues

  • Always verify NDA/ANDA status for drug products before purchase.
  • Look for FDA recall notices and verify product listing before use.
  • Consider safer, FDA-approved OTC motion sickness products when shopping.

Documentation advice

Keep packaging, recall notices, and correspondence with the manufacturer. Take photos of packaging and product labels.

Product Details

Product: Taoscare Motion Sickness Patches, 36-count boxes Brand: ibspot Manufacturer: Henan Xinyongtal Medical Technology., Ltd. Address: he nan sheng zhou kou shi huai yang xian gong ye yuan qu, X003SR097N Sold by/Distribution: Wyoming and Virginia (WY and VA) Recall date: 2025-10-09 Recall number: D-0098-2026 Status: ACTIVE Hazard: Marketed Without an Approved NDA/ANDA Remedy: Stop using the product and contact ibspot or your healthcare provider for guidance Link to recall: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0098-2026

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • 3 boxes recalled
  • 36-count box
  • NDA/ANDA issue
  • Distributed in WY and VA
  • Active recall as of 2025-10-29
  • Recall number D-0098-2026

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
4/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Brand
Affected States
WY, VA
Report Date
October 29, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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