CLASS II ONGOING Drug recall · Reported 11 Dec 2024 · FDA Enforcement Report
10 Irregular Pigmentation, Accelerator recalled by Generitech
Generitech is recalling 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature +, distributed in California. The recall was initiated on 22 Nov 2024 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0111-2025
- FDA event ID
- 95819
- Recalling firm
- Generitech, Fresno, CA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 22 Nov 2024
- FDA classified
- 5 Dec 2024
- Reported
- 11 Dec 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Manufacturing (CGMP) Deviations
Timeline
| 22 Nov 2024 | Recall initiated by company | |
| 5 Dec 2024 | Classified by FDA | +13 days |
| 11 Dec 2024 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations: Inconsistency in the water systems.
Product as listed by the FDA
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.
Where it was distributed
CA
Questions about this recall
Is 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature + recalled?
Yes. Generitech recalled 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature + on 22 Nov 2024. The recall is Class II and its status is Ongoing. Recall number D-0111-2025.
Why was it recalled?
CGMP Deviations: Inconsistency in the water systems.
Which lots are affected?
Lot #: 2400017, Exp: 4/30/2026
Where was it sold?
CA
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.