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Beckman Coulter

MedTech Current publications and recall entries tagged Beckman Coulter.

Device RecallsFDA Class II Recall Watch: 16–22 August 2026

Beckman Coulter recalls DxC 500 analyzers over calculated-rule software defect

The defect is notable because a software import can silently change laboratory calculation logic rather than producing an obvious system failure. Laboratories determine whether predefined rules were modified and whether results need retrospective review.