FDA Adverse Event Death Summary report: N

BED-CHECK SENSORMAT

MDR report key: 293267 · Received August 17, 2000

Report

Report Number
1640702-2000-00003
Event Type
Death
Date Received
August 17, 2000
Date of Event
July 20, 2000
Report Date
August 17, 2000
Manufacturer
BED-CHECK CORP
Product Code
KMI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PT WAS FOUND AT APPROX 12:15AM BY CNA AND ORIENTEE, LAYING ON THE SIDE, ON THE FLOOR NEXT TO THE BED WITH THE HEAD IN WASTE RECEPTICLE. PT HAD A BED ALARM AND 2, 1/2 SIDERAILS. 1 SIDERAIL DOWN WHEN STAFF FOUND PT AND LIGHT ON OVER DOOR AND AT NURSE'S STATION, BUT NO SOUND EMITTING FROM BED ALARM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BED-CHECK SENSORMAT BED ALARM KMI BED-CHECK CORP 30 DAY *

Patients

Seq Age Sex Outcome Treatment
1 92 YR Death BED-CHECK ALARM