FDA Adverse Event Malfunction Summary report: N

4 MOTOR ADVANCE BED

MDR report key: 1190713 · Received October 6, 2008

Report

Report Number
1824206-2008-03707
Event Type
Malfunction
Date Received
October 6, 2008
Date of Event
September 8, 2008
Report Date
September 8, 2008
Manufacturer
HILL-ROM RITTER
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE HOSPITAL MAINTENANCE PERSON REPORTED THAT THE SCALE ACCURACY ON THIS BED IS OFF BY 10LBS. AFTER TROUBLESHOOTING WITH A HILL-ROM TECHNICIAN, IT WAS DISCOVERED THAT THE SCALE LOAD BEAMS WERE LOOSE, AND NEEDED TO RETIGHTENED. THERE WERE NO ADVERSE EVENTS ASSOCIATED WITH THIS PRODUCT PROBLEM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 4 MOTOR ADVANCE BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1165 NA

Patients

Seq Age Sex Outcome Treatment
1