CS300 INTRA-AORTIC BALLOON PUMP Adverse Event — Malfunction (MDR 10004520)
CS300 INTRA-AORTIC BALLOON PUMP Adverse Event — Malfunction (MDR 10004520) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CS300 INTRA-AORTIC BALLOON PUMP; Generic name: SYSTEM, BALLOON, INTRA-AORTIC AND CONTROL; Manufacturer: DATASCOPE CORP..
| Device | CS300 INTRA-AORTIC BALLOON PUMP |
|---|---|
| Generic name | SYSTEM, BALLOON, INTRA-AORTIC AND CONTROL |
| Manufacturer | DATASCOPE CORP. |
| Report number | 10004520 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Narrative | WITH 2 DOCTORS WENT TO CT FOR AN EMERGENCY ABDOMINAL CT. UPON ARRIVAL TO CT, THE BALLOON PUMP SHUT DOWN. WE WERE AT CT AT THIS POINT AND WE PLUGGED IT IN IMMEDIATELY BUT IT WOULD NOT TURN BACK ON. WE IMMEDIATELY CALLED THE CCU AND PUSHED A NEW BALLOON PUMP DOWN AND WE SWITCHED IT OUT. |
| Source | openFDA MAUDE (device adverse events) |
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