10 Irregular Pigmentation — Class II drug recall D-0111-2025
Ongoing recall by Generitech Corporation, reported 2024-12-11, distributed in CA. CGMP Deviations: Inconsistency in the water systems.
| Recall number | D-0111-2025 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Generitech Corporation, Fresno, CA, United States |
| Recall initiated | 2024-11-22 |
| Classified | 2024-12-05 |
| Reported by FDA | 2024-12-11 |
| Distributed | CA |
| Quantity | 77.5 pounds |
| Reason classes | cgmp |
| Lot numbers | 2400017 |
| Expiration dates | 2026-04-30 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0111-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.