FHF Farmhouse Fresh, Midnight Clearing, NIGHT LOTION, 2.5% BENZOYL PEROXIDE ACNE TREATMENT, OTC a) 0.5 fl. oz./15ml; and
Summary
The FDA issued a Class II for FHF Farmhouse Fresh, Midnight Clearing, NIGHT LOTION, 2.5% BENZOYL PEROXIDE ACNE by Owen Biosciences Inc.. Reason: Chemical contamination: Presence of benzene.
Details
Source
Drug Recall
External ID
D-0452-2026
Action Date
2026-04-22
Status
Ongoing
Category
drug
Product Description
FHF Farmhouse Fresh, Midnight Clearing, NIGHT LOTION, 2.5% BENZOYL PEROXIDE ACNE TREATMENT, OTC a) 0.5 fl. oz./15ml; and b)1 fl. oz./30ml tubes; Made in the USA for FarmHouse Fresh, 8797 CR 858 McKinney, Texas
Lot/Code Info: Lot #2595500, Exp.10/2/2026 Lot #2549700, Exp.6/12/2026 Lot #2638200, Exp.4/30/2027
Quantity Affected: 7,975 tubes
Reason for Recall
Chemical contamination: Presence of benzene
Distribution
U.S. Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-03
Company
Baton Rouge, LA
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 94 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Owen Biosciences Inc. has 4 FDA actions in our database, including 4 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 (Owen Biosciences Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Owen Biosciences Inc. have FDA actions?
Owen Biosciences Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0452-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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