10 Irregular Pigmentation recall
FDA recall D-0111-2025 · initiated Nov 22, 2024
Generitech Corporation recalled 10 Irregular Pigmentation in Nov 2024 — an FDA Class II recall (D-0111-2025) because CGMP Deviations: Inconsistency in the water systems.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
CGMP Deviations: Inconsistency in the water systems.
The manufacturing process itself
The FDA found the process itself out of compliance, usually before any defective product was identified.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: 77.5lbs
Details
- Product
- 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.
- Recalling company
- Generitech Corporation
- Classification
- Class II
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- CA
- Initiated
- Nov 22, 2024
- FDA report date
- Dec 11, 2024
Frequently asked
- Was 10 Irregular Pigmentation recalled?
- Generitech Corporation recalled 10 Irregular Pigmentation in Nov 2024 — an FDA Class II recall (D-0111-2025) because CGMP Deviations: Inconsistency in the water systems. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was 10 Irregular Pigmentation recalled?
- Per the FDA enforcement record, the reason for recall D-0111-2025 was: CGMP Deviations: Inconsistency in the water systems.
- Is a recalled 10 Irregular Pigmentation dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of 10 Irregular Pigmentation are affected?
- Distributed: CA. The recall covers these lots — Lot #: 2400017, Exp: 4/30/2026. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0111-2025.