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ELITech Group B.V Recalls

1 recall on record · October 9, 2019 to October 9, 2019 · Medical Devices

October 9, 2019Medical DevicesFDA

ELITech Group B.V. recalls Viva-ProE Systems, Model # 6003-670, UDI: 03661540600357 - Product Usage: The ELITech Clinical Systems Selectra ProM is

Hazard: Software malfunction; The action being taken due to the device becoming inoperable due to software lockup.

ELITech Group B.V Recalls | RecallWatchUSA