840 VENTILATOR Adverse Event — Malfunction (MDR 8020893-2008-00072)
840 VENTILATOR Adverse Event — Malfunction (MDR 8020893-2008-00072) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 840 VENTILATOR; Generic name: VENTILATOR; Manufacturer: PURITAN-BENNETT CORPORATIONS.
| Device | 840 VENTILATOR |
|---|---|
| Generic name | VENTILATOR |
| Manufacturer | PURITAN-BENNETT CORPORATIONS |
| Report number | 8020893-2008-00072 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, User facility, Company representation |
| Narrative | THE SERVICE REPORT SHOWS THE CUSTOMER REPORTED THAT THE 840 VENTILATOR STOPPED CYCLING WHILE IN USE ON A PT. THE PT WAS NOT HARMED OR INJURED AS A RESULT OF THE EVENT. |
| Source | openFDA MAUDE (device adverse events) |
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