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Beckman Coulter Biomedical Gmbh Recalls

4 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Beckman Coulter Biomedical Gmbh.

4Total Recalls
0Critical
47Units Affected
Jul 17, 2024Most Recent
All Recalls

Every Beckman Coulter Biomedical Gmbh Recall

Sorted by most recent. Click any recall for full details.

4 recalls
High RiskFDA
Beckman Coulter Biomedical Gmbh
PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.
Medical Devices·0 affected·Jul 17, 2024
High RiskFDA
Beckman Coulter Biomedical Gmbh
Power Express, REF B90918
Medical Devices·0 affected·Jul 17, 2024
High RiskFDA
Beckman Coulter Biomedical Gmbh
Beckman Coulter DxA Automation System, DxA 5000 Fit, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly
Medical Devices·15 affected·Jun 2, 2023
High RiskFDA
Beckman Coulter Biomedical Gmbh
DxA 5000; Catalog Number:B50516; UDI:15099590707118 - Product Usage: The DxA 5000 is a high-speed, modular, automated sample handling sys...
Diagnostic Devices·32 affected·Jun 17, 2020