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Medium severity

MicroScan Neg MIC 3J REF C54814

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateJune 25, 2025
ReportedApril 15, 2026
Recalling firmBeckman Coulter, Inc.
Country / regionUnited States CA

Hazard

Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics

Affected products

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