HEART LUNG MACHINE Adverse Event — Malfunction (MDR 8010762-2020-00139)
HEART LUNG MACHINE Adverse Event — Malfunction (MDR 8010762-2020-00139) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: HEART LUNG MACHINE; Generic name: PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE; Manufacturer: MAQUET CARDIOPULMONARY GMBH.
| Device | HEART LUNG MACHINE |
|---|---|
| Generic name | PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE |
| Manufacturer | MAQUET CARDIOPULMONARY GMBH |
| Report number | 8010762-2020-00139 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER, FOREIGN, HEALTH PROFE |
| Narrative | COMPLAINT ID: (B)(4). |
| Source | openFDA MAUDE (device adverse events) |
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