FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1821777 · Received August 26, 2010

Report

Report Number
1824206-2010-09603
Event Type
Malfunction
Date Received
August 26, 2010
Date of Event
August 3, 2010
Report Date
August 3, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH FOUND THE HEX ROD ON THE CASTER WAS LOOSE AND NOT ALLOWING THE BRAKE TO SET. THE TECH RESET THE HEX ROD AND TIGHTENED UP THE BOLT TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE CASTER ON RIGHT FOOT OF THE BED IS NOT HOLDING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1