The production device history record (dhr) for this intra-aortic balloon pump (iabp) unit was reviewed and no non-conformance's related to the reported event were noted.A getinge service territory manager (stm) was dispatched to evaluate the iabp unit.The stm was not able to reproduce the problem.After checking the error logs, a bad executive processor board (epb) was found.The stm replaced the epb and completed all safety, functionality, and calibration checks and all tests passed to factory specifications.The iabp unit was cleared for clinical use and released to the customer.
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