FDA Adverse Event Death Summary report: N

UNK

MDR report key: 41546 · Received October 2, 1996

Report

Report Number
2022906-1996-00005
Event Type
Death
Date Received
October 2, 1996
Date of Event
July 17, 1996
Report Date
October 2, 1996
Manufacturer
SPACELABS MED, INC.
Product Code
MHX
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

ALARMS ON BEDSIDE FOUND OFF AND PT HAD OXYGEN SATURATION OF 40%.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNK BEDSIDE MONITOR MHX SPACELABS MED, INC. 90303A UNK

Patients

Seq Age Sex Outcome Treatment
1 31 YR Death