RecallHawk
Class II Recall

Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%), 0.33 oz. (9.45 g), Distributed by Alchemee LLC, Santa Monica, C

Alchemee, LLC

Summary

The FDA issued a Class II for Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%), 0.33 oz. (9.45 g), Dist by Alchemee, LLC. Reason: Chemical contamination: Presence of benzene.

Details

Source

Drug Recall

External ID

D-0359-2025

Action Date

2025-04-16

Status

Ongoing

Category

drug

Product Description

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,

Lot/Code Info: Lots V3304A, V3305A, Exp 10/31/2025

Quantity Affected: 38,237 bottles

Reason for Recall

Chemical contamination: Presence of benzene

Distribution

Nationwide in the USA

Type: Voluntary: Firm initiated

Recall Initiated: 2025-03-12

Company

Alchemee, LLC

Hawthorne, NY

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 86 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

Alchemee, LLC has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Alchemee, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Alchemee, LLC have FDA actions?

Alchemee, LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0359-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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