FDA Adverse Event Malfunction Summary report: N

BED CHECK CORDLESS SENSORMAT

MDR report key: 6259922 · Received January 18, 2017

Report

Report Number
6259922
Event Type
Malfunction
Date Received
January 18, 2017
Date of Event
October 25, 2016
Report Date
November 25, 2016
Manufacturer
STANLEY SECURITY SOLUTIONS, INC.,
Product Code
KMI
Product Problem
Yes
Report Source
User Facility report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

BED CHECK PAD WOULD NOT CONNECT TO THE DEVICE. ANOTHER PAD WAS OBTAINED AND CONNECTED WITHOUT DIFFICULTY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
44132 BED CHECK CORDLESS SENSORMAT MONITOR, BED PATIENT KMI STANLEY SECURITY SOLUTIONS, INC., 73050 A0516

Patients

Seq Age Sex Outcome Treatment
1 90 YR