PNEUPAC PARAPAC PLUS Adverse Event — Malfunction (MDR 3012307300-2020-03395)
PNEUPAC PARAPAC PLUS Adverse Event — Malfunction (MDR 3012307300-2020-03395) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PNEUPAC PARAPAC PLUS; Generic name: VENTILATOR, EMERGENCY, POWERED (RESUSCITATOR); Report number: 3012307300-2020-03395.
| Device | PNEUPAC PARAPAC PLUS |
|---|---|
| Generic name | VENTILATOR, EMERGENCY, POWERED (RESUSCITATOR) |
| Report number | 3012307300-2020-03395 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | USER FACILITY |
| Narrative | INFORMATION WAS RECEIVED INDICATING THAT A SMITHS MEDICAL PNEUPAC PARAPAC PLUS WAS CYCLING ON AND OFF. IT WAS REPORTED THAT A NEW BATTERY HAD BEEN INSERTED BUT STILL WAS GIVING A LOW-PRESSURE ALERT ALONG WITH A LOW BATTERY ALERT. THERE WERE NO REPORTED ADVERSE EFFECTS. |
| Source | openFDA MAUDE (device adverse events) |
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