Catalog Number 0998-00-3023-53 |
Device Problem
Appropriate Term/Code Not Available (3191)
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Patient Problems
No Known Impact Or Consequence To Patient (2692); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/19/2021 |
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 fse performed a pumping test which was normal.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 prior to use the cs300 intra-aortic balloon pump (iabp) helium tank could not be detected.There was no patient involvement, and no adverse event reported.
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Event Description
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It was reported that prior to use the cs300 intra-aortic balloon pump (iabp) helium tank could not be detected.There was no patient involvement, and no adverse event reported.
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Search Alerts/Recalls
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