FDA Drugs recall ·
LILAS Feminine Pain Relief Patch, Menthol 10%, a) 5 patches per box ( recall
- Recall number
- D-0069-2025
- Date
- (initiated October 24, 2024)
- Company / brand
- Unexo Life Sciences Private Limited
B16, Sector 4, Bawana Industrial Area, New Delhi, India - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Terminated
- Units affected
- 363,300 patches
- Hazard tags
- Manufacturing practices (cGMP)
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
LILAS Feminine Pain Relief Patch, Menthol 10%, a) 5 patches per box (UPC 7 87099 48212 1) and 10 patches per box (UPC 7 87099 48211 4), Distributed by: Lilas Wellness, Inc., Beaverton, Oregon 97008-7105
Why was it recalled?
cGMP Deviations
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
a) UPC 7 87099 48212 1 b) UPC 7 87099 48211 4
Distribution
Nationwide in the US
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0069-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.