FDA Adverse Event Malfunction Summary report: N

3 MOTOR ADVANCED BED

MDR report key: 1063841 · Received June 19, 2008

Report

Report Number
1824206-2008-02707
Event Type
Malfunction
Date Received
June 19, 2008
Date of Event
June 3, 2008
Report Date
June 5, 2008
Manufacturer
HILL-ROM RITTER
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

REPORTER REPORTED THAT SHE UNLOCKED THE BRAKES TO POSITION THE BED FOR A PATIENT TRANSFER. DENISE STATED THAT THE LEFT FOOT CASTER MOVED DOWNWARD. RN, REPORTED THAT THE PATIENT RECEIVED A RED MARK ON THEIR LEFT ARM DUE TO THE BED MOVING DOWNWARD. THEY APPLIED ICE TO THE PATIENT'S ARM AND THE PATIENT WAS OK. THE HILL-ROM TECHNICIAN FOUND THAT THE LEFT FOOT LEG EXTENSION HAD SEPARATED FROM THE BASEFRAME, DUE TO A BROKEN WELD. THE BASEFRAME WAS REPLACED TO RESOLVE THE ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 3 MOTOR ADVANCED BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1130 NA

Patients

Seq Age Sex Outcome Treatment
1