# FDA recall D-0111-2025

> **Generitech Corporation** · Class II · drug recall initiated 2024-11-22.

## 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.

## Distribution

CA

## Key facts

- **Recall number:** D-0111-2025
- **Recalling firm:** Generitech Corporation
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2024-11-22
- **Report date:** 2024-12-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fresno, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0111-2025

## Citation

> AI Analytics. FDA recall D-0111-2025. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-0111-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
