TERUMO PERFUSION SYSTEM 8000 Adverse Event — Malfunction (MDR 1828100-2008-00090)
TERUMO PERFUSION SYSTEM 8000 Adverse Event — Malfunction (MDR 1828100-2008-00090) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TERUMO PERFUSION SYSTEM 8000; Generic name: HEART LUNG CONSOLE; Manufacturer: TERUMO CARDIOVASCULAR SYSTEMS CORP..
| Device | TERUMO PERFUSION SYSTEM 8000 |
|---|---|
| Generic name | HEART LUNG CONSOLE |
| Manufacturer | TERUMO CARDIOVASCULAR SYSTEMS CORP. |
| Report number | 1828100-2008-00090 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Health Professional, User facility |
| Narrative | DURING PREVENTIVE MAINTENANCE, THE DEVICE DID NOT SWITCH FROM BATTERY BACKUP TO AC POWER AS EXPECTED. THERE WAS NO REPORTED ADVERSE CONSEQUENCE TO THE PT AS A RESULT OF THIS EVENT. |
| Source | openFDA MAUDE (device adverse events) |
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