Blaine Labs recalls Fungal Fusion Antifungal Solution due to discontinued stability testing, risking product effectiveness and safety. Affected units include specific lot numbers and expiration dates.
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
Blaine Labs is recalling their Fungal Fusion Antifungal Solution and related products because they stopped required stability testing for items still within their expiration date. This could mean the products might not work as intended or could be unsafe.
The recall is due to Blaine Labs discontinuing required stability testing for products still within their expiration date. This means the products might not be as effective or could pose safety risks if used without proper testing.
People who own or use the Fungal Fusion Antifungal Solution, Antimicrobial Kit, or related products with lot number BL3572 manufactured by Blaine Labs. Those using the product for medical purposes may be at slightly higher risk.
Check for the lot number BL3572 on the product label. The product was manufactured by Blaine Labs, Inc. and expires April 16, 2028.
Look for the lot number BL3572 on the Fungal Fusion Antifungal Solution or related products.
Blaine Labs discontinued required stability testing for products still within their expiration date, which could affect product effectiveness and safety.
Check the product label for the lot number BL3572. If you have it, contact Blaine Labs for further instructions.
The recall is due to potential effectiveness and safety issues from discontinued stability testing, but no specific serious injury risk is mentioned.
We’ve drafted a message you can send Blaine Labs to request your refund or repair — edit it as you like.
Subject: Recall D-0698-2026 — Blaine Labs Blaine Labs Hello, I own a Blaine Labs that is covered by recall D-0698-2026 from Blaine Labs. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
