G4: 26may2020.B4: 22sep2020.It was clarified that this event did not occur during patient use.This event was evaluated by the customer in-house there was no on-site evaluation by the manufacturer.The customer reported that after performance verification testing, no issue could be found.No further repair was documented.The device was then returned to service.Submission of a report does not constitute an admission that medical personnel, user facility, importer, distributor, manufacturer, or product caused or contributed to the event.
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