CLASS II ONGOING Drug recall · Reported 16 Apr 2025 · FDA Enforcement Report

Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%) recalled

Alchemee is recalling Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%), distributed nationwide in the US. The recall was initiated on 12 Mar 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots V3304A, V3305A, Exp 10/31/2025
Quantity recalled38,237 bottles

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-0359-2025
FDA event ID
96508
Recalling firm
Alchemee, Hawthorne, NY
Classification
Class II
Status
Ongoing
Recall initiated
12 Mar 2025
FDA classified
9 Apr 2025
Reported
16 Apr 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Benzene

Timeline

12 Mar 2025Recall initiated by company
9 Apr 2025Classified by FDA+28 days
16 Apr 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Chemical contamination: Presence of benzene

Product as listed by the FDA

Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%), 0.33 oz. (9.45 g), Distributed by Alchemee LLC, Santa Monica, CA 90401, Made in the USA, UPC 7 35786 01921 1, UPC 8 42944 10223 1, and also packaged as a twin pack UPC 8 42944 10241 5,

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Chemical contamination: Presence of benzene

Which lots are affected?

Lots V3304A, V3305A, Exp 10/31/2025

Where was it sold?

Nationwide in the USA

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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 96508

This product is part of a recall event; the main page for the event is Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%) recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IIProactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%) recalledAlchemeeBenzeneNationwide

More recalls from Alchemee

All 2
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIProactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%) recalledAlchemeeBenzeneNationwide