FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 1883924 · Received October 22, 2010

Report

Report Number
1824206-2010-10614
Event Type
Malfunction
Date Received
October 22, 2010
Date of Event
September 28, 2010
Report Date
September 28, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH FOUND GREASE ON THE HI/LOW DRIVE BRAKE DRUM. THE TECH CLEANED THE HI/LOW DRIVE BRAKE DRUM ASSEMBLY TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE HI/LOW DRIFTS DOWN AFTER RELEASING THE DOWN CONTROL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CENTRA BED AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 850

Patients

Seq Age Sex Outcome Treatment
1