PULMONETIC Adverse Event — Injury (MDR 2031702-2008-00038)
PULMONETIC Adverse Event — Injury (MDR 2031702-2008-00038) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PULMONETIC; Generic name: VOLUME VENTILATOR; Manufacturer: CARDINAL HEALTH 203/PULMONETIC SYSTEM, INC..
| Device | PULMONETIC |
|---|---|
| Generic name | VOLUME VENTILATOR |
| Manufacturer | CARDINAL HEALTH 203/PULMONETIC SYSTEM, INC. |
| Report number | 2031702-2008-00038 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, Distributor |
| Narrative | VENTILATOR ALARMS DO NOT SEEM LOUD EVEN WHEN SET TO 80DB. |
| Source | openFDA MAUDE (device adverse events) |
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