Blaine Labs recalls vite20 Antifungal Cream (10% Undecylenic Acid) due to discontinued stability testing, potentially affecting product safety. Learn if you have the product and what to do.
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
Blaine Labs is recalling vite20 Antifungal Cream because they stopped required stability testing for products still within their expiration date. This could mean the product isn't safe for use as intended.
The product was made without completing necessary stability testing, which is required by regulatory standards to ensure it remains safe and effective over time. This could lead to the product not working properly or being unsafe for use.
People who own or use the vite20 Antifungal Cream (10% Undecylenic Acid) bottle with lot number BL3462, manufactured by Blaine Labs, Inc. in Sante Fe Springs, California.
Check for the product name 'vite20 Antifungal Cream', 0.54 oz (15 g) bottle, lot number BL3462, and expiration date 2/7/2027. The product was manufactured by Blaine Labs, Inc. in Sante Fe Springs, California.
Look for the lot number BL3462 and expiration date 2/7/2027 on the product label.
The recall states that stability testing was discontinued, which could affect product safety, but the official notice does not specify if the product is unsafe to use.
Check for the product name 'vite20 Antifungal Cream', 0.54 oz (15 g) bottle, lot number BL3462, and expiration date 2/7/2027.
The recall record does not specify a remedy, so the official notice does not state what action to take.
We’ve drafted a message you can send Blaine Labs to request your refund or repair — edit it as you like.
Subject: Recall D-0696-2026 — Blaine Labs Blaine Labs Hello, I own a Blaine Labs that is covered by recall D-0696-2026 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.
