Class II

Medical Device Recall: Yeastone Broth, 11ML, 10/BOX YY3462

Remel, Inc · March 24, 2026

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.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Vietnam, France, Argentina, Qatar, New Zealand, Uruguay, Turkey, Netherlands, Singapore.

States Affected

NATIONWIDE

Quantity Affected

2819

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1806-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.