AUTOCAT2 WAVE Adverse Event — Malfunction (MDR 1219856-2008-00050)
AUTOCAT2 WAVE Adverse Event — Malfunction (MDR 1219856-2008-00050) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: AUTOCAT2 WAVE; Generic name: INTRA-AORTIC BALLOON PUMP PRODUCTS; Manufacturer: ARROW INTL., INC..
| Device | AUTOCAT2 WAVE |
|---|---|
| Generic name | INTRA-AORTIC BALLOON PUMP PRODUCTS |
| Manufacturer | ARROW INTL., INC. |
| Report number | 1219856-2008-00050 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | User facility |
| Narrative | IT WAS REPORTED THAT WHILE TRANSPORTING A PT, THE PUMP'S BATTERY "DIED." FIELD SERVICE WAS PHONED AND THE FOLLOWING IS A LIST OF THE FINDINGS AND THE ACTIONS TAKEN: FUSES CHECKED - REPLACED POWER SUPPLY, PERFORMED FUNCTIONAL CHECK - PASSED, PERFORMED ELECTRICAL SAFETY CHECK - PASSED. UNIT WAS RETURNED TO FACILITY ON 02/05/08. |
| Source | openFDA MAUDE (device adverse events) |
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