ELITech Group B.V Viva-ProE Systems, Model # 6003-670, UDI: 03661540600357 - Product Usage recall — FDA Z-2764-2019
Software malfunction; The action being taken due to the device becoming inoperable due to software lockup.
Overview of recall records associated with ELITech Group B.V., including dates, categories and classifications where available.
Classification mix: Class III: 1.
Software malfunction; The action being taken due to the device becoming inoperable due to software lockup.
This page summarizes recall records in which the official source identifies ELITech Group B.V. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.