SERVO-I Adverse Event — Malfunction (MDR 1225700-2008-00013)
SERVO-I Adverse Event — Malfunction (MDR 1225700-2008-00013) 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 | 1225700-2008-00013 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-01 |
| Narrative | THE CUSTOMER REPORTED THAT WHILE THE VENTILATOR WAS CONNECTED TO A PT THREE TECHNICAL ERRORS INDICATING INTERNAL 12V POWER FAILURE, BATTERY LOW AND EXCEEDED BAROMETER LOWER LIMIT VALUE WERE GENERATED. VENTILATION CONSEQUENTLY STOPPED. THERE WAS NO PT INJURY. |
| Source | openFDA MAUDE (device adverse events) |
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