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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Topical Products

Proactiv Acne Treatments Recalled for Benzene Contamination

Agency Publication Date: April 9, 2025
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Summary

Alchemee, LLC is recalling approximately 41,737 bottles of Proactiv Skin Smoothing Exfoliator (benzoyl peroxide 2.5%) and Proactiv Emergency Blemish Relief (benzoyl peroxide 5%). These topical acne treatments, sold in various sizes including 6 oz. bottles and 0.33 oz. tubes, are being recalled due to the presence of benzene, a chemical contaminant. The recall includes specific lots of the exfoliator and the emergency blemish relief products distributed nationwide.

Risk

Benzene is classified as a human carcinogen. Long-term exposure to benzene through inhalation, oral intake, or skin contact can potentially lead to cancers such as leukemia and other blood disorders.

What You Should Do

  1. This recall affects Proactiv Skin Smoothing Exfoliator and Proactiv Emergency Blemish Relief acne treatments sold in 6 fl. oz. bottles, 0.33 oz. tubes, and twin packs.
  2. Check your products for the following lot numbers and expiration dates: lot V4204A (Exp 07/31/2025) for the Skin Smoothing Exfoliator, and lots V3304A or V3305A (Exp 10/31/2025) for the Emergency Blemish Relief.
  3. Verify the UPC barcodes on your product packaging: 735786015282, 842944102231, 735786019211, or 842944102415.
  4. If you have health concerns, contact your healthcare provider or pharmacist.
  5. Return any unused product to the place of purchase for a refund, throw it away, or contact Alchemee, LLC for further instructions.
  6. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%)
Variants: 6 fl. oz. (177.4 mL), 0.33 OZ (9.45g), 2.5% Strength
UPC Codes:
735786015282
842944102231
Lot Numbers:
V4204A (Exp 07/31/2025)

Distributed by Alchemee, LLC, Santa Monica, CA 90401.

Product: Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%)
Variants: 0.33 oz. (9.45 g), Twin Pack, 5% Strength
UPC Codes:
735786019211
842944102231
842944102415
Lot Numbers:
V3304A (Exp 10/31/2025)
V3305A (Exp 10/31/2025)

Distributed by Alchemee LLC, Santa Monica, CA 90401.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96508
Status: Active
Manufacturer: Alchemee, LLC
Sold By: Retailers nationwide; Online retailers
Manufactured In: United States
Units Affected: 2 products (38,237 bottles; 3,500 bottles)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.