FDA Adverse Event
Injury
Summary report: N
VAPORIZER FRO NORTH AMERICAN DRAGER
MDR report key: 26216
·
Received September 13, 1995
Report
- Report Number
- 2517967-1995-00027
- Event Type
- Injury
- Date Received
- September 13, 1995
- Date of Event
- August 23, 1995
- Report Date
- September 13, 1995
- Manufacturer
- OHMEDA
- Product Code
- CAD
- Adverse Event
- Yes
- Report Source
- Distributor report
- Reporter Location
- CO, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE PT WAS DIAGNOSED WITH PULMONARY EDEMA WHEN COMING OUT OF RECOVERY FROM A SURGERY THAT DAY. THE PT HAD BEEN ANESTHETIZED WITH DESFLURANE, A NARCOTIC AND O2. THE PT WAS GIVEN LASIX TO PREVENT FURTHER DEVELOPMENT OF AND REVERSE THE PULMONARY EDEMA. THE PT RESPOND APPROPIATELY AND QUICKLY AND HAD BEEN RELEASED FROM THE HOSP. THE VAPORIZER HAS BEEN REMOVED FROM SERVICE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VAPORIZER FRO NORTH AMERICAN DRAGER | DEFLURANE VAPORIZER | CAD | OHMEDA | TEC-6 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Required Intervention |