FDA Drug Recalls

Recalls / Class II

Class IID-0067-2025

Product

HealthWise PERIOD PATCH Menstrual Pain Relief, Menthol 10%, 10 patches per box, Manufactured for Veridian Healthcare, LLC, Gurnee, IL 60031 NDC 71101-947-10, UPC 8 45717 01072 6

Brand name
Healthwise Menstrual Pain Relief Patch
Generic name
Menthol
Active ingredient
Menthol, Unspecified Form
Route
Topical
NDC
71101-947
FDA application
M017
Affected lot / code info
UPC 8 45717 01072 6

Why it was recalled

cGMP Deviations

Recalling firm

Firm
Unexo Life Sciences Private Limited
Manufacturer
Veridian Healthcare
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
B16, Sector 4, Bawana Industrial Area, New Delhi, N/A, India

Distribution

Quantity
10,368 patches
Distribution pattern
Nationwide in the US

Timeline

Recall initiated
2024-10-24
FDA classified
2024-11-22
Posted by FDA
2024-12-04
Terminated
2025-09-16
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0067-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: Healthwise Menstrual Pain Relief Patch · FDA Drug Recalls