Medications & Supplements/Topical Products

Only Your Rx Pigment Fading Activator Recalled for Water System Inconsistency

Agency Publication Date: December 5, 2024

Summary

Generitech Corporation is recalling 78 units (approximately 77.5 lbs) of Only Your Rx (Nature + Science) 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator. The recall affects 1 fl. oz. (30 mL) bottles intended for professional use only. This action was taken due to inconsistencies discovered in the water systems during the manufacturing process, which deviate from required quality standards.

Risk

Issues with water systems during manufacturing can lead to product quality issues or potential contamination. While no specific health incidents have been reported, consumers should stop using the product to avoid potential adverse reactions.

What You Should Do

This recall affects Only Your Rx (Nature + Science) 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, sold in 1 fl. oz. (30 mL) bottles.
Identify affected products by checking for Lot # 2400017 with an expiration date of 4/30/2026 on the label.
Stop using the recalled product immediately.
If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Generitech Corporation for further instructions.
Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

Option 1: Full Refund

How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund

Option 2: Dispose of Product

How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature + Science (1 fl. oz. / 30 mL)by Only Your Rx

Variants: For Professional Use Only

Lot Numbers:

2400017 (Exp 4/30/2026)

Distributed in 30 mL bottles; manufactured by Generitech Corporation in Fresno, CA.

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 95819

Status: Active

Manufacturer: Generitech Corporation

Sold By: Only YourRx Inc.

Manufactured In: United States

Units Affected: 77.5lbs

Distributed To: California

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.

Summary

What You Should Do

This recall affects Only Your Rx (Nature + Science) 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, sold in 1 fl. oz. (30 mL) bottles.

Identify affected products by checking for Lot # 2400017 with an expiration date of 4/30/2026 on the label.

Stop using the recalled product immediately.

If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Generitech Corporation for further instructions.

Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.