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