FDA Drugs recall ·
10 Irregular Pigmentation, Accelerator, Pigment Fading Activator… recall
- Recall number
- D-0111-2025
- Date
- (initiated November 22, 2024)
- Company / brand
- Generitech Corporation
4967 E Lansing Way, Fresno, CA, United States - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 77.5lbs
- Hazard tags
- Manufacturing practices (cGMP)
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature + Science, 1 fl. oz., 30 mL Bottle, For Professional Use Only, Only YourRx Inc., Chatsworth, CA 91311, Made in USA, Onlyyourrx.com.
Why was it recalled?
CGMP Deviations: Inconsistency in the water systems.
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
Lot #: 2400017, Exp: 4/30/2026
Distribution
CA
States: California
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-0111-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.