Generitech Corporation recalls 10 units of Only Your Rx Pigment Fading Activator due to water system inconsistencies in manufacturing. This may affect product consistency and safety for professional use.
CGMP Deviations: Inconsistency in the water systems.
Generitech Corporation is recalling 10 units of their Pigment Fading Activator product because of water system inconsistencies during manufacturing. This could lead to inconsistent product quality and potential safety issues for professional users.
The product was manufactured with inconsistent water systems, which could lead to variations in the product's composition. This may affect the product's effectiveness and safety for professional use.
Professional users of this product are likely affected. Those using the product for medical purposes should be cautious as it's intended for professional use only.
Check for the product name '10 Irregular Pigmentation, Accelerator, Pigment Fading Activator' on a 1 fl. oz. bottle labeled 'Only Your Rx'. The lot number 2400017 and expiration date 4/30/2026 are also associated with this recall.
Verify the product name, lot number, and expiration date to confirm if it's part of the recall.
The recall is due to water system inconsistencies during manufacturing, which may affect product consistency and safety for professional use. The product is intended for professional use only.
Generitech Corporation is recalling 10 units of this product.
The recall does not specify a remedy, so check the product details to confirm if it's part of the recall.
We’ve drafted a message you can send Only Your Rx to request your refund or repair — edit it as you like.
Subject: Recall D-0111-2025 — Only Your Rx Only Your Rx Hello, I own a Only Your Rx that is covered by recall D-0111-2025 from Only Your Rx. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
