HomeMedical Device recalls
Medium severity

Yeastone Broth, 11ML, 10/BOX YY3462

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateMarch 24, 2026
ReportedApril 22, 2026
Recalling firmRemel, Inc
Country / regionUnited States KS

Hazard

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.

Affected products

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