FDA Adverse Event Malfunction Summary report: N

CCU BED

MDR report key: 2033896 · Received March 23, 2011

Report

Report Number
1824206-2011-01793
Event Type
Malfunction
Date Received
March 23, 2011
Date of Event
March 1, 2011
Report Date
March 1, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THAT THE CASTERS STEMS WERE BROKEN. HE REPLACED THE FOOT CASTERS AND THE BRAKES FUNCTIONED PROPERLY.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES WHEN THE BRAKE IS ENGAGED, THE CASTERS AT THE FOOT END OF THE BED WOULD STILL SWIVEL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CCU BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 894

Patients

Seq Age Sex Outcome Treatment
1