Patient identifier was not provided.Livanova (b)(4) manufactures the s5 roller pump.The incident occurred in (b)(6).This medwatch report is being filed on behalf of livanova (b)(4).A livanova field service representative was dispatched to the facility to investigate.The service representative was able to confirm the reported issue and traced the failure to a faulty power switch, which was replaced to resolve the issue.Subsequent functional verification testing was completed without further issues and the unit was returned to service.The replaced part was returned to livanova (b)(4) for further evaluation.A defect was identified in the switch that would not allow it to latch properly when mounted.A supplier quality notification was initiated to inform the supplier of the defect.A review of the dhr did not identify any deviations or non-conformities relevant to the reported issue.If any additional information pertinent to the reported event is received, it will be provided in a supplemental report.
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