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ACTIVE RECALL — CLASS IIActive recallD-0273-2025/FDA enforcement
Zapzyt Acne Treatment Gel·Cosmetics·Feb 24, 2025

Zapzyt, Acne Treatment Gel, 10% Benzoyl Peroxide Gel, Packaged in 1 OZ (28.35g) Tube, …

What you need to know

Class II

  • What happened

    Chemical Contamination: Presence of benzene.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A known human carcinogen that can be introduced through contaminated ingredients or manufacturing processes.

  • Action required

    Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement.

Active recall · classified by the FDANationwide (US)More cosmetics

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Product identification

Source: FDA COSMETICS

Brand nameZapzyt Acne Treatment Gel
Recalling firmDenison Pharmaceuticals, LLCLincoln, RI, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot #: 9762, Exp. Date 2/28/2025; 9763, 9764, 9765, Exp. Date 3/31/2025; 9869, 9870, Exp. Date 5/31/2025; 9871, 9872, Exp. Date 7/31/2025; 9996, 9997, 9998, Exp. Date 8/31/2025; 9995, Exp. Date 10/31/2025
  • 0154, 0153, 0326, Exp. Date 1/31/2026; 0155, 0156, 0161, 0327, 0329, 0328, Exp. Date 2/28/2026; 0479, 0480, Exp. Date 5/31/2026.
Distribution area
Nationwide

Nationwide within the USA

United States

Quantity affected642, 131 tubes
Recall initiationFDA report date: March 19, 2025
FDA recall numberD-0273-2025

Beyond the headline

The recall, in context

Denison Pharmaceuticals, LLC initiated this cosmetics recall on February 24, 2025. The FDA enforcement report states: Chemical Contamination: Presence of benzene. The FDA report lists distribution as: Nationwide within the USA.

The FDA enforcement report describes the reason as: Chemical Contamination: Presence of benzene.

Zapzyt, Acne Treatment Gel, 10% Benzoyl Peroxide Gel, Packaged in 1 OZ (28.35g) Tube, … was made or distributed by Denison Pharmaceuticals, LLC in Lincoln, RI, United States. This page reflects FDA report D-0273-2025, dated March 19, 2025.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a known human carcinogen that can be introduced through contaminated ingredients or manufacturing processes.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Set the product aside and do not apply it.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Benzene contamination

Possible health effects

Benzene is a known human carcinogen. Long-term exposure is associated with blood disorders and cancer. A recall is a precautionary step to reduce exposure.

When symptoms may appear

Health effects are generally associated with repeated or long-term exposure rather than a single incubation period.

Higher-risk groups

People who use the affected product frequently, pregnant people, children and people with existing blood disorders should be especially cautious.

What to do now

  1. 1Stop using the affected cosmetic or personal-care product immediately.
  2. 2Keep the package and contact the retailer or manufacturer about a refund or replacement; do not use it as a substitute.
  3. 3If you have concerns about exposure or symptoms, speak with a healthcare professional.

Benzene is a known human carcinogen; this information is not a personal exposure assessment.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Zapzyt, Acne Treatment Gel, 10% Benzoyl Peroxide Gel, Packaged in 1 OZ (28.35g) Tube, … recall?

Zapzyt Acne Treatment Gel recalled Zapzyt, Acne Treatment Gel, 10% Benzoyl Peroxide Gel, Packaged in 1 OZ (28.35g) Tube, … in an FDA Class II enforcement action reported as D-0273-2025. Chemical Contamination: Presence of benzene.

What should I do if I bought this product?

Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement. Stop using the affected cosmetic or personal-care product immediately. Keep the package and contact the retailer or manufacturer about a refund or replacement; do not use it as a substitute. If you have concerns about exposure or symptoms, speak with a healthcare professional.

Is the Zapzyt Acne Treatment Gel recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D-0273-2025. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.