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FDAClass II · Drug · Recalled July 8, 2026

Fungal Fusion ERADICATION Solution recall — Blaine Labs Inc

Hazard: CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
D-0698-2026
Brand
Blaine Labs
Classification
Class II
Units affected
1,500 bottles
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Description

Fungal Fusion ERADICATION Solution, Antifungal & Antimicrobial Kit. Contains, 1x2 oz bottle Fungal Fusion Antifungal (Miconazole Nitrate) Cream, 1x2oz bottle Fungal Fusion Antifungal Solution (25% Undecylenic Acid) and 1x1oz bottle of Fungal Fusion Eradication Antimicrobial Show Spray (isopropyl Alcohol, D-Limonene, Undecylenic Acid). Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Santa Fe Springs, CA 90670, Manufactured for Doctor's Inc

Affected products

Companies & origin

Recalling firm location
Santa Fe Springs, CA, United States
Firm address
11037 Lockport Pl, N/A, 90670-4634

Identifying details (verbatim from the notice)

Product codes / lots
Lot BL3572, Exp 04/16/2028
Distribution
Nationwide in the USA
Firm notified the public via
Press Release
FDA event ID
98731
Recall initiated
April 8, 2026
FDA classified
July 16, 2026
FDA report date
July 8, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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