Warning
Remel Recalls Yeastone Broth, 11ML, 10/BOX YY3462
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 #Z-1806-2026Medical Device
Remel Recalls Yeastone Broth, 11ML, 10/BOX YY3462
Remel, Inc · Class II — Moderate Risk
Product Description
Yeastone Broth, 11ML, 10/BOX YY3462
Reason for Recall
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.
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
Worldwide distribution - US Nationwide and the countries of Canada, Vietnam, France, Argentina, Qatar, New Zealand, Uruguay, Turkey, Netherlands, Singapore.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA classified this recall as Class II, indicating the medical device may cause temporary health problems or poses a slight threat of a serious nature. Remel, Inc initiated the recall on March 24, 2026 affecting 2819. Products may report incorrect AST results during quality control. The product was distributed internationally, including the United States. Consumers should check their purchases and discontinue use of any affected product. Contact Remel, Inc for further instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Other Injury Hazards.