FDA Adverse Event
Injury
Summary report: N
DRAGER
MDR report key: 724221
·
Received May 18, 2006
Report
- Report Number
- MW1039267
- Event Type
- Injury
- Date Received
- May 18, 2006
- Date of Event
- May 10, 2006
- Report Date
- May 18, 2006
- Manufacturer
- DRE, INC
- Product Code
- CBK
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- TX, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
STAFF CALLED TO PT'S ROOM DUE TO SCREEN ON THE DRAGER VENT OUT. THE PT CONTINUED TO BE VENTILATED BY DRAGER MACHINE. THE SATURATIONS NEVER DROPPED BELOW 96%. THE PT HAD GOOD BILATERAL CHEST EXPANSION. PT NEVER IN ANY DISTRESS. DRAGER VENT SWITCHED OUT AND THE PT PLACED ON A NEW VENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DRAGER | VENTILATOR | CBK | DRE, INC | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 20 YR | Disability |