Generitech Corporation: Drug Recall
Recall #D-0111-2025 · 11/22/2024
Class II: Risk
Recall Details
- Recall Number
- D-0111-2025
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Generitech Corporation
- Status
- Ongoing
- Date Initiated
- 11/22/2024
- Location
- Fresno, CA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 77.5lbs
Reason for Recall
CGMP Deviations: Inconsistency in the water systems.
Product Description
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.
Distribution Pattern
CA
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.