Catalog Number 0998-00-0800-53 |
Device Problem
Unexpected Shutdown (4019)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 04/09/2021 |
Event Type
malfunction
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Manufacturer Narrative
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A getinge field service engineer (fse) was dispatched to evaluate this unit.The biomed stated the batteries were depleted and charged the iabp overnight.The fse was unable to reproduce the issue.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 while in use on a patient, the cardiosave intra-aortic balloon pump (iabp) screen was not working.No patient harm, serious injury or adverse event was reported.
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Event Description
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It was reported that while in use on a patient, the cardiosave intra-aortic balloon pump (iabp) screen was not working.No patient harm, serious injury or adverse event was reported.
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Search Alerts/Recalls
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