Warning
Blaine Labs Inc Recalls Fungal Fusion ERADICATION Solution
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0698-2026Drug / Pharmaceutical
Blaine Labs Inc Recalls Fungal Fusion ERADICATION Solution
Blaine Labs Inc · Class II — Moderate Risk
Product 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
Reason for Recall
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
Nationwide in the USA
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
Blaine Labs Inc has recalled a pharmaceutical product that the FDA classified as Class II affecting 1,500 bottles. The recall was initiated on April 8, 2026. CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry. It was distributed nationwide. Class II recalls involve products that might cause a temporary health problem or pose only a slight threat of a serious nature. Consumers should discontinue use and contact the firm.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medication Defects.