Patient information was not provided.Livanova (b)(4) manufactures the s5 cardioplegia sensor module.The incident occurred in (b)(6).This medwatch report is being filed on behalf of livanova (b)(4).The customer reported that the defect only occurred once and that they have had no other issues with the unit following the event.A livanova field service representative was dispatched to the facility to investigate.The service representative was unable to duplicate the reported issue.As the issue could not be reproduced, a root cause was not determined.If any additional information pertinent to the reported event is received, it will be provided in a supplemental report.Device not returned.
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