FDA Recall D-0111-2025
Generitech Corporation · Fresno, CA
Class II Ongoing 538 days on record
Moderate impact — Class II recall — temporary or medically reversible adverse health consequence possible; remote probability of serious adverse health consequence.
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.
Reason for recall
CGMP Deviations: Inconsistency in the water systems.
Recall record
- Recall number
D-0111-2025- Classification
- Class II
- Status
- Ongoing
- Voluntary or mandated
- Voluntary: Firm initiated
- Firm notification
- Distribution
- CA
- Recall initiated
- 2024-11-22
- Classified by FDA Center
- 2024-12-05
- FDA published
- 2024-12-11
- Recalling firm
- Generitech Corporation
- Firm location
- Fresno, CA
Operational response
Class II recalls indicate possible temporary or reversible health consequences. Remove affected lots from active dispensing. Segregate inventory. Check the firm’s recall notification for guidance on patient outreach.
For the official FDA enforcement record, see FDA's Recall Search.