FDA Adverse Event Malfunction Summary report: N

P850 CENTRA BED

MDR report key: 1190650 · Received October 3, 2008

Report

Report Number
1824206-2008-03704
Event Type
Malfunction
Date Received
October 3, 2008
Date of Event
September 10, 2008
Report Date
September 10, 2008
Manufacturer
HILL-ROM RITTER.
Product Code
FNL
Report Source
Manufacturer report
Reporter Location
HI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE HI-LOW DRIFTING IS UNINTENTIONAL MOVEMENT OF THE BED WHICH HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN CLEANED AND LUBRICATED THE HI-LOW DRIVE IN ORDER TO RESOLVE THE PROBLEM. ALL BED DRIVES ARE REQUIRED TO BE INSPECTED, CLEANED, AND LUBRICATED AT LEAST ONCE A YEAR IN ACCORDANCE WITH THE PRODUCT SERVICE MANUAL.

Description of Event or Problem · 1

A TECHNICIAN DISCOVERED THAT THIS BED WOULD DRIFT DOWN FROM THE UP POSITION. THERE WAS NO PATIENT IN THE BED AT THAT TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 P850 CENTRA BED AC POWERED HOSPTIAL BED FNL HILL-ROM RITTER. P850 NA

Patients

Seq Age Sex Outcome Treatment
1