Catalog Number 0998-00-0800-53 |
Device Problem
Power Problem (3010)
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Patient Problem
No Patient Involvement (2645)
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Event Date 01/28/2021 |
Event Type
malfunction
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Manufacturer Narrative
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A getinge field service engineer (fse) was dispatched to evaluate this unit.The iabp was not completely inserted into the cart.The fse secured the unit into the cart.The iabp charged properly.The fse 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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Event Description
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It was reported that the cardiosave intra-aortic balloon pump (iabp) was not detecting ac power.There was no patient involvement, and no adverse event reported.
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Event Description
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It was reported that the cardiosave intra-aortic balloon pump (iabp) was not detecting ac power.There was no patient involvement, and no adverse event reported.
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Search Alerts/Recalls
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