RecallHawk
Class II Recall

Benzoyl Peroxide Wash, USP, 5%, 5 FL OZ (148 mL), Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite

SV Labs Toronto Corporation

Summary

The FDA issued a Class II for Benzoyl Peroxide Wash, USP, 5%, 5 FL OZ (148 mL), Distributed by: Rugby Laborato by SV Labs Toronto Corporation. Reason: Microbial contamination of topical product..

Details

Source

Drug Recall

External ID

D-0878-2026

Action Date

2026-10-07

Status

Ongoing

Category

drug

Product Description

Benzoyl 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/Code Info: Lot #: 0525-02-345, Exp. Date 02/2027

Reason for Recall

Microbial contamination of topical product.

Distribution

IL only

Type: Voluntary: Firm initiated

Recall Initiated: 2026-09-01

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 23 drug recalls issued in the same week, part of 40 drug-related FDA actions this month.

SV Labs Toronto Corporation has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (SV Labs Toronto Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does SV Labs Toronto Corporation have FDA actions?

SV Labs Toronto Corporation has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0878-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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