FDA recall D-0879-2026 · Oct 7, 2026
SV Labs Toronto Corporation: Benzoyl Peroxide Wash recall
Product
Benzoyl 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.
Reason for recall
Microbial contamination of topical product.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- 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
- Distribution
- IL only
- Recalling firm
- SV Labs Toronto Corporation, Brampton
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-09-01
Source: openFDA enforcement record D-0879-2026 · search recall number D-0879-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 12:58 AM EDT. The agency notice is the final word.
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