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Use caution Drug recall · FDA · Published September 1, 2026

SV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination

SV Labs Toronto Corporation recalls specific lots of Benzoyl Peroxide Wash, USP 10% due to microbial contamination. Check your bottle's lot number and expiration date.

🇺🇸 FDA recall #D-0879-2026DrugSV Labs ›
✎ GovInfoNow plain-language explainer

What happened, in plain English

SV Labs Toronto Corporation is recalling Benzoyl Peroxide Wash, USP, 10%, because the product may be contaminated with microorganisms. The recall affects specific lots of both 5 FL OZ and 8.5 FL OZ bottles distributed in Illinois. Consumers should check their products against the listed lot numbers to see if they are affected. Read more at govinfonow.com/recall/1443849-sv-labs-toronto-corporation-recalls-benzoyl-peroxide-wash-usp-10.

Source Summary by GovInfoNow · govinfonow.com/recall/1443849-sv-labs-toronto-corporation-recalls-benzoyl-peroxide-wash-usp-10 · Published October 13, 2026 · Updated October 13, 2026 · FDA enforcement record: FDA #D-0879-2026

Cite this page

“SV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/1443849-sv-labs-toronto-corporation-recalls-benzoyl-peroxide-wash-usp-10. Based on FDA recall #D-0879-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0879-2026%22&limit=1).

Why it’s dangerous

The product is contaminated with microorganisms, which can pose a health risk when applied to the skin. This could potentially lead to skin infections or other adverse reactions in users.

Who’s affected

Individuals in Illinois who purchased Benzoyl Peroxide Wash, USP 10% from the recalled lots. Users of topical acne treatments are at risk of skin irritation or infection from the contamination.

How to tell if you have this one

Look for Benzoyl Peroxide Wash, USP, 10% in either 5 FL OZ (NDC 0536-1261-63) or 8.5 FL OZ (NDC 0536-1351-42) bottles. Check the lot numbers: for 5 FL OZ, lots are 0575-01-366 and 0565-02-336; for 8.5 FL OZ, lots are 0645-02-355, 0575-02-336, and 0565-12-317. Verify expiration dates: Jan-27, Feb-27, or Dec-26.

  • Brand
    SV Labs
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    IL only
Recall numberProduct, codes & lotsQuantity
D-0878-2026Benzoyl Peroxide Wash, USP, 5%, 5 FL OZ (148 mL), Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1259-63; Lot #: 0525-02-345, Exp. Date 02/2027—
D-0879-2026Benzoyl Peroxide Wash, USP, 10%, packaged in a)5 FL OZ (148mL) bottles (NDC 0536-1261-63), and b) 8.5 FL OZ (237 mL) bottles (NDC 0536-1351-42), Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152.; a) Lot #: 0575-01-366, Exp. Date Jan-27; 0565-02-336, Exp. Date FEB-27; b) Lot #: 0645-02-355, 0575-02-336, Exp. Date Feb-27; 0565-12-317, Exp. Date Dec-26—
Based on the official FDA remedy

What to do — step by step

  1. Check your product

    Compare the lot number and expiration date on your Benzoyl Peroxide Wash bottle against the recalled lots listed in the record.

  2. Stop using contaminated bottles

    If your product matches the recalled lot numbers, stop using it immediately to avoid potential microbial exposure.

Where it went and when

Where it was distributed

Distributed in Illinois.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “IL only” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois.

Recall timeline

FDA published this recall 36 days after the firm started it.

1. Firm started the recall: Sep 1, 202612. FDA classified it Class II: Sep 30, 202623. Published in FDA’s Enforcement Report: Oct 7, 202634. Added to GovInfoNow: Oct 13, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0879-2026 (September 1, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0879-2026 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 13, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA