FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2253852 · Received August 11, 2011

Report

Report Number
1824206-2011-04252
Event Type
Malfunction
Date Received
August 11, 2011
Date of Event
July 31, 2011
Report Date
August 1, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECH FOUND SERVICE CODE 20-49 AND RIGHT INTERMEDIATE CABLE WITH INTERMITTENT CONNECTION WAS NOT WORKING CORRECTLY. FOUND OLD FLUID RESIDUE ON UCM BOARD. REPLACED RIGHT INTERMEDIATE CABLE AND UCM BOARD TO CORRECT PROBLEM. BED IN STORAGE AREA.

Description of Event or Problem · 1

CUSTOMER STATED THAT SERVICE REQUIRED LIGHT WAS FLASHING. NO ALLEGED INJURIES BY ACCOUNT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900

Patients

Seq Age Sex Outcome Treatment
1