Drug & medication recalls Moderate risk

10 Irregular Pigmentation recalled over manufacturing violations

Recall date
November 22, 2024
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Generitech Corporation recalls 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature + Science, 1 fl. oz., 30 mL Bott…
Recall number
D-0111-2025
FDA classification
Class II
Brand / firm
Generitech Corporation
Sold / distributed
CA

Why it was recalled

CGMP Deviations: Inconsistency in the water systems.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.

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