840 VENTILLATOR Adverse Event — Malfunction (MDR 8020893-2008-00071)
840 VENTILLATOR Adverse Event — Malfunction (MDR 8020893-2008-00071) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 840 VENTILLATOR; Generic name: VENTILLATOR; Manufacturer: PURITAN-BENNETT CORP.
| Device | 840 VENTILLATOR |
|---|---|
| Generic name | VENTILLATOR |
| Manufacturer | PURITAN-BENNETT CORP |
| Report number | 8020893-2008-00071 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, User facility, Company representation |
| Narrative | THE SVC REPORT SHOWS THE CUSTOMER REPORTED THAT THE 840 VENTILATOR STOPPED CYCLING WHILE IN USE ON THE PT. THE PT WAS NOT HARMED OR INJURED AS A RESULT OF THE EVENT. THE PURITAN BENNETT CUSTOMER SUPPORT ENGINEER (CSE) VERIFIED THE MALFUNCTION. THE CSE INSPECTED THE DEVICE AND REPLACED THE MOTHERBOARD AND AI BOARD. THE UNIT PASSED EXTENDED SELF TESTING. |
| Source | openFDA MAUDE (device adverse events) |
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