Generitech Irregular Pigmentation Recall: FDA Class II

Why it was recalled

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.

Lot numbers, UPCs & expiration codes

Lot #: 2400017, Exp: 4/30/2026

Where it was sold

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-0111-2025
Classification: Class II
Status: Ongoing
Recall initiated: Nov 22, 2024
FDA report date: Dec 11, 2024
Quantity: 77.5lbs
Recall type: Voluntary: Firm initiated
Recalling firm: Generitech Corporation

Original FDA data

Every field from FDA enforcement report D-0111-2025, exactly as published.

Show all FDA fields

City: Fresno
State: CA
Status: Ongoing
Country: United States
Event ID: 95819
Address: 4967 E Lansing Way
Code information: Lot #: 2400017, Exp: 4/30/2026
Postal code: 93727-7408
Report date: Dec 11, 2024
Product type: Drugs
Recall number: D-0111-2025
Classification: Class II
Recalling firm: Generitech Corporation
Product quantity: 77.5lbs
Reason for recall: CGMP Deviations: Inconsistency in the water systems.
Voluntary / mandated: Voluntary: Firm initiated
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
Recall initiation date: Nov 22, 2024
Initial firm notification: E-Mail
Center classification date: Dec 5, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0111-2025, published Dec 11, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

Generitech 10 Irregular Pigmentation Recall

Summary