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Sep 30, 2020newest stored source record
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Medical DeviceSep 30, 2020

Beckman Coulter Biomedical GmbH DxA 5000 recall — FDA Z-2983-2020

The DxA 5000 instructions for use may be confusing regarding the re-use of sample IDs. Beckman Coulter has received complaints where the re-use of sample barcodes were not being detected by…

Class IIFDA: TerminatedBeckman Coulter Biomedical GmbH
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