FDA Adverse Event Death Summary report: N

BCI PULSE PATIENT CABLE

MDR report key: 431911 · Received December 4, 2002

Report

Report Number
431911
Event Type
Death
Date Received
December 4, 2002
Date of Event
September 20, 2002
Report Date
November 20, 2002
Manufacturer
SIMS BCI, INC
Product Code
DSA
Report Source
User Facility report
Reporter Location
KY, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

WHEN A PERSON WENT INTO REPOSITION PT THEY FOUND PT WAS UNRESPONSIVE. THERE WAS NO INDICATOR LIGHT AT THE NURSES STATION, BUT ALARM WAS SOUNDING IN THE ROOM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BCI PULSE PATIENT CABLE MONITORING EXTENSION CABLE DSA SIMS BCI, INC 3311 *

Patients

Seq Age Sex Outcome Treatment
1 64 YR Death