Model Number N/A |
Device Problem
Connection Problem (2900)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 02/14/2020 |
Event Type
malfunction
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Manufacturer Narrative
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The production device history record (dhr) for this iabp unit was unable to be reviewed as we were not able to obtain the serial number for the iabp associated with this complaint.A getinge service territory manager (stm) was dispatched to evaluate the iabp unit.A supplemental report will be submitted when additional information is provided.
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Event Description
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It was reported that the intra-aortic balloon pump (iabp) alarmed iab disconnected.All the connections were secure and the safety disk was in the appropriate position.There was no blood seen in the iab helium tubing.The customer switched pumps and the alarms stopped.It is unknown if there was any patient harm/injury; however there was no adverse event reported.
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Manufacturer Narrative
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After further investigation, it has been confirmed that this complaint event has been already reported in another emdr.Please refer to mfg report number: 2249723-2020-00390 for complete information on this complaint event.
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Event Description
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It was reported that the intra-aortic balloon pump (iabp) alarmed iab disconnected.All the connections were secure and the safety disk was in the appropriate position.There was no blood seen in the iab helium tubing.The customer switched pumps and the alarms stopped.It is unknown if there was any patient harm/injury; however there was no adverse event reported.
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Search Alerts/Recalls
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