SERVO-I Adverse Event — Malfunction (MDR 1225700-2008-00012)
SERVO-I Adverse Event — Malfunction (MDR 1225700-2008-00012) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SERVO-I; Generic name: CBK; Manufacturer: MAQUET CRITICAL CARE AB.
| Device | SERVO-I |
|---|---|
| Generic name | CBK |
| Manufacturer | MAQUET CRITICAL CARE AB |
| Report number | 1225700-2008-00012 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-01 |
| Narrative | IT WAS REPORTED THAT THE VENTILATOR FAILED THE INTERNAL LEAKAGE, FLOW TRANSDUCER AND PRESSURE TRANSDUCER TEST DURING PRE USE CHECK. |
| Source | openFDA MAUDE (device adverse events) |
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