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Bd Diagnostic Recalls

1 recall on record · April 26, 2017 to April 26, 2017 · Medical Devices

April 26, 2017Medical DevicesFDA

Bd Diagnostic recalls BD Viper LT software, version 3.00H

Hazard: BD has confirmed reports that lower than expected RFU values were generated on customer BD Viper LT Systems after the installation of software version 3.00H. As RFU values decrease, results approach the assay cutoff threshold which has the potential to impact test results.

Bd Diagnostic Recalls | RecallWatchUSA