HIGHFDA DRUG

Torrey Pines Benzaderm BPO Cleanser 10% Recall Over Benzene Contamination, 2025

Torrey Pines Dermatology & Laser Center's Benzaderm BPO Cleanser recall remains active. The FDA-listed recall covers benzoyl peroxide cleanser lot numbers 58170A and 58172A with expiration 09/2025. Consumers should stop use and contact the recall coordinator.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
September 12, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
September 12, 2025
Hazard Level
HIGH
Brand
Private Label Skin Care
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
2 states
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Private Label Skin Care
Product type
BPO Cleanser (benzoyl peroxide)
Model numbers
Lot # 58170A, Lot # 58172A
Sizes
7 oz (201 g)
Sold at
Unknown
Where affected
CA, GA

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    September 12, 2025

  2. Reported by FDA DRUG

    October 1, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Private Label Skin Care Inc. or your healthcare provider for guidance. Notification method: Letter

About This Product

A benzoyl peroxide cleanser used for acne treatment. Sold under a private-label brand and distributed in CA and GA.

Why This Is Dangerous

Benzene exposure is a known carcinogen. Contaminated cleansers pose health risks through topical exposure.

Industry Context

This recall is not described as part of a broader industry pattern in the provided data.

Real-World Impact

Immediate product withdrawal reduces exposure risk. Consumers should await recall guidance for refunds or replacements.

Practical Guidance

How to identify if yours is affected

  1. Check lot numbers 58170A and 58172A on the product packaging
  2. Verify expiration date 09/2025
  3. Review recall notice from FDA page

Where to find product info

FDA recall page and enforcement report D-0665-2025

What timeline to expect

Refund or replacement processing timelines will be provided by the recall coordinator; expect weeks to a couple of months

If the manufacturer is unresponsive

  • Document all communications
  • Escalate to FDA consumer complaint if needed
  • Consider consumer protection agency contact if company is unresponsive

How to prevent similar issues

  • Verify ingredient safety recalls before purchase
  • Choose trusted brands with transparent testing data
  • Keep packaging until disposal or refund is complete

Documentation advice

Retain receipt, packaging, lot number, expiration date, and all recall notices

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Product Details

Brand: Private Label Skin Care. Product: Benzaderm BPO Cleanser 10% 7 oz (201 g). Model/Lot: Lot # 58170A and 58172A. Expiration: 09/2025. Distribution: California and Georgia. Recall date: 2025-09-12. Status: ACTIVE.

Reported Incidents

No specific injuries or illnesses are reported in the provided data.

Key Facts

  • Hazard Level: HIGH
  • Brand: Private Label Skin Care
  • Product: Benzaderm BPO Cleanser 10% 7 oz (201 g)
  • Lot: 58170A and 58172A Exp: 09/2025

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
POISONINGELECTRICALOTHER

Product Details

Model Numbers
Lot # 58170A
Lot # 58172A
Affected States
CA, GA
Report Date
October 1, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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