Medical DeviceJun 14, 2017
Nexstim eXima NBS System Software version 2.2 or higher recall — FDA Z-2319-2017
Software defect: the NBS software may accidentally generate duplicate copies of one or several files.
Class IIFDA: OngoingNexstim PLC
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceJun 14, 2017
Nexstim PLC NBS System 4 (sw version 4.0 or higher), Software update to 4.3.3 and NBS System recall — FDA Z-2320-2017
Software defect: the NBS software may accidentally generate duplicate copies of one or several files.
Class IIFDA: OngoingNexstim PLC
Understanding this recall history
This page summarizes recall records in which the official source identifies Nexstim PLC 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.