PRIMUS Adverse Event — Death (MDR 9611500-2008-00005)
PRIMUS Adverse Event — Death (MDR 9611500-2008-00005) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRIMUS; Generic name: ANESTHESIA WORKSTATION; Manufacturer: DRAEGER MEDICAL AG & CO. KG.
| Device | PRIMUS |
|---|---|
| Generic name | ANESTHESIA WORKSTATION |
| Manufacturer | DRAEGER MEDICAL AG & CO. KG |
| Report number | 9611500-2008-00005 |
| Event type | Death |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Foreign, Health Professional, User facility |
| Narrative | IT WAS REPORTED, AFTER UNEVENTFUL INDUCTION OF ANESTHESIA AND SURGERY, SUDDENLY IT WAS NOT POSSIBLE TO APPLY O2-FLUSH OR BREATHING PRESSURE TO THE PT. THE ANESTHESIA DEVICE WAS IMMEDIATELY CHANGED AND EMERGENCY ACTIONS ON THE PT WERE PERFORMED. THE PT EXPIRED IN THE THEATRE. |
| Source | openFDA MAUDE (device adverse events) |
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