Could cause temporary or reversible harm; serious harm is unlikely.
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
| Distributed by / for | Doctor's Inc |
| Full product label | 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 |
| Recalling firm | Blaine Labs Inc |
| Distribution | Nationwide in the USA |
| Quantity | 1,500 bottles |
| Recall initiated | 2026-04-08 |
| Report date | 2026-07-08 |
| Recall completed | — |
| Recall number | D-0698-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Santa Fe Springs CA United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗