10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature + Science, 1 fl. oz., 30 mL Bottl
Summary
The FDA issued a Class II for 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, by Generitech Corporation. Reason: CGMP Deviations: Inconsistency in the water systems..
Details
Source
Drug Recall
External ID
D-0111-2025
Action Date
2024-12-11
Status
Ongoing
Category
drug
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/Code Info: Lot #: 2400017, Exp: 4/30/2026
Quantity Affected: 77.5lbs
Reason for Recall
CGMP Deviations: Inconsistency in the water systems.
Distribution
CA
Type: Voluntary: Firm initiated
Recall Initiated: 2024-11-22
Company
Fresno, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 64 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Generitech Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Generitech Corporation have FDA actions?
This is the only FDA action we have on record for Generitech Corporation in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0111-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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