Remel recalls Yeastone Broth (11ML, 10/BOX YY3462) due to potential incorrect lab results causing delayed antifungal treatment. Affected lots include 321046, 329835, 330316, 327069, 330317, 336325, 338314, 341161, 303851, 311723.
Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores Quality Control test result.
Remel is recalling Yeastone Broth (11ML, 10/BOX YY3462) because it may give incorrect lab results during quality control. This could lead to delayed treatment or needing a different antifungal drug if the lab ignores the test results.
The Yeastone Broth may produce incorrect results during quality control checks. If the lab ignores these results, it could delay treatment or require switching to another antifungal medication.
Users of Yeastone Broth for laboratory testing are affected. Lab technicians and healthcare providers who use this product for antifungal testing are most at risk.
Check the lot numbers on the packaging: 321046, 329835, 330316, 327069, 330317, 336325, 338314, 341161, 303851, 311723. The product is labeled as Yeastone Broth, 11ML, 10/BOX YY3462.
Look for lot numbers 321046, 329835, 330316, 327069, 330317, 336325, 338314, 341161, 303851, or 311723 on the packaging.
The product may report incorrect AST results during quality control, which could lead to delayed treatment or needing a different antifungal agent if the lab ignores the test results.
Check the lot numbers on the packaging. If it matches the listed lots, contact Remel for guidance.
The recall is for potential lab errors, not physical injury risks. The hazard is low risk as it relates to test accuracy, not direct harm.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-1806-2026 — Remel Remel Hello, I own a Remel that is covered by recall Z-1806-2026 from Remel. 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.
