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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