Model Number 0998-00-0800-53 |
Device Problem
Device Displays Incorrect Message (2591)
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Patient Problems
Insufficient Information (4580); Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/18/2023 |
Event Type
malfunction
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Event Description
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It was reported that the cardiosave intra-aortic balloon pump (iabp) safety disc repair needed.
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Manufacturer Narrative
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A supplemental report will be submitted upon completion of our investigation.
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Event Description
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It was reported that the cardiosave intra-aortic balloon pump (iabp) safety disc repair needed.There was no patient involvement reported.
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Manufacturer Narrative
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Record is being cancelled as it was opened in error.Revert all sections to blank : b.Adverse event or product problem d.Suspect medical device e.Initial reporter g.All manufacturers h.Device manufacturers only.
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Event Description
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Record is being cancelled as it was opened in error.
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Search Alerts/Recalls
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