Model Number N/A |
Device Problem
Unexpected Shutdown (4019)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 02/09/2021 |
Event Type
malfunction
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Manufacturer Narrative
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A getinge field service engineer (fse) was dispatched to evaluate the iabp and was unable to reproduce the reported issue.The fse replaced was the console cover screw kit that is required for inspection.Unit passed all functional and safety test per factory specifications.The iabp was then released to the customer and cleared for clinical service.
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Event Description
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It was reported that during use on a patient, the cardiosave intra-aortic balloon pump (iabp) unit shut down.The patient was connected to another unit to continue therapy.No patient harm, serious injury or adverse event was reported.
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Event Description
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It was reported that during use on a patient, the cardiosave intra-aortic balloon pump (iabp) unit shut down.The patient was connected to another unit to continue therapy.No patient harm, serious injury or adverse event was reported.
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Search Alerts/Recalls
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